On the public citation graph
Cortistatins A, B, C, and D, Anti-angiogenic Steroidal Alkaloids, from the Marine Sponge Corticium simplex
0 signed · 298 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0040-4020(94)01015-ropenalex-snapshot
Constituents of cimicifugae rhizoma II. Isolation and structures of new cycloartenol triterpenoids and related compounds from Cimicifuga foetida L
inferredcites →https://doi.org/10.1016/j.tet.2005.05.038openalex-snapshot
Efficient total synthesis of bastadin 6, an anti-angiogenic brominated tyrosine-derived metabolite from marine sponge
inferredcites →https://doi.org/10.1016/s0040-4020(01)88180-1openalex-snapshot
Five new steroidal alkaloids from buxus papilosa. Some relationships between structures and specific rotations
inferredcites →https://doi.org/10.1016/s0040-4039(98)01655-4openalex-snapshot
A new steroidal alkaloid from a marine sponge Corticium sp
inferredcites →https://doi.org/10.1056/nejm199512283332608openalex-snapshot
Clinical Applications of Research on Angiogenesis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4466.1.4zenodo-depositor-declared
New sciaphilic plakinids (Porifera, Homoscleromorpha) from the Central-Western Pacific
inferred← citeshttps://doi.org/10.1002/0471264180.or115.01openalex-snapshot
(4+3) Cycloadditions of Allylic and Related Cations
inferred← citeshttps://doi.org/10.1002/9781118120392.ch4openalex-snapshot
Electronic CD Exciton Chirality Method: Principles and Applications
inferred← citeshttps://doi.org/10.1002/9781118342886.ch9openalex-snapshot
Domino Reactions in the Enantioselective Synthesis of Bioactive Natural Products
inferred← citeshttps://doi.org/10.1002/9781118596784.ssd021openalex-snapshot
Cascade Reactions in Stereoselective Synthesis
inferred← citeshttps://doi.org/10.1002/9781118778173.ch12openalex-snapshot
A Formal [3+3] Cycloaddition Approach To Natural Product Synthesis
inferred← citeshttps://doi.org/10.1002/9781118778173.ch19openalex-snapshot
Application of The [4+3] Cycloaddition Reaction To The Synthesis of Natural Products
inferred← citeshttps://doi.org/10.1002/9781118940228.ch10openalex-snapshot
Natural Product Synthesis for Drug Discovery and Chemical Biology
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod019openalex-snapshot
Porifera (Sponges)–1
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod195openalex-snapshot
Porifera (Sponges)–5
inferred← citeshttps://doi.org/10.1002/9783527621071.ch9openalex-snapshot
Antiangiogenic Alkaloids from Marine Organisms
inferred← citeshttps://doi.org/10.1002/9783527654628.ch10openalex-snapshot
Oxidations in C–C Bond Building
inferred← citeshttps://doi.org/10.1002/9783527671304.ch14openalex-snapshot
Domino Reactions in the Total Synthesis of Natural Products
inferred← citeshttps://doi.org/10.1002/9783527698479.ch13openalex-snapshot
Total Synthesis of Complex Natural Products via Dearomatization
inferred← citeshttps://doi.org/10.1002/adsc.200900864openalex-snapshot
Divergent Reactivity of 2‐Azetidinone‐Tethered Allenols with Electrophilic Reagents: Controlled Ring Expansion versus Spirocyclization
inferred← citeshttps://doi.org/10.1002/adsc.201301153openalex-snapshot
Advancement in Cascade [1,n]‐Hydrogen Transfer/Cyclization: A Method for Direct Functionalization of Inactive C(sp3)H Bonds
inferred← citeshttps://doi.org/10.1002/adsc.201600218openalex-snapshot
Regio‐ and Stereoselective Syntheses of 7‐Oxabicyclo[2.2.1]heptanes via a Gold(I)‐Catalyzed Cycloisomerization of Alkynediols: Asymmetric Total Synthesis of Farnesiferol C
inferred← citeshttps://doi.org/10.1002/adsc.70438openalex-snapshot
Transition Metal‐Catalyzed Functionalization of Nonallylic Alkenyl Alcohols via Chain‐Walking Strategies
inferred← citeshttps://doi.org/10.1002/ange.200802203openalex-snapshot
Rapid Construction of the Cortistatin Pentacyclic Core
inferred← citeshttps://doi.org/10.1002/ange.200803550openalex-snapshot
Total Synthesis of (+)‐Cortistatin A
inferred← citeshttps://doi.org/10.1002/ange.200803720openalex-snapshot
Highlights der Steroidchemie: chemische Totalsynthese versus Semisynthese
inferred← citeshttps://doi.org/10.1002/ange.200901116openalex-snapshot
Stereodivergent Synthesis of 17‐α and 17‐β‐Aryl Steroids: Application and Biological Evaluation of D‐Ring Cortistatin Analogues
inferred← citeshttps://doi.org/10.1002/ange.200904565openalex-snapshot
Brønsted Acid Catalyzed Enantioselective Semipinacol Rearrangement for the Synthesis of Chiral Spiroethers
inferred← citeshttps://doi.org/10.1002/ange.200904778openalex-snapshot
Cortistatin A is a High‐Affinity Ligand of Protein Kinases ROCK, CDK8, and CDK11
inferred← citeshttps://doi.org/10.1002/ange.201104769openalex-snapshot
A Versatile Synthesis of Substituted Isoquinolines
inferred← citeshttps://doi.org/10.1002/ange.201202699openalex-snapshot
Asymmetric Syntheses of 8‐Oxabicyclo[3,2,1]octanes: A Cationic Cascade Cyclization
inferred← citeshttps://doi.org/10.1002/ange.201204274openalex-snapshot
Organocatalytic Asymmetric Direct CH Functionalization of Ethers: A Highly Efficient Approach to Chiral Spiroethers
inferred← citeshttps://doi.org/10.1002/ange.201204469openalex-snapshot
Enantioselektive Titan(III)‐katalysierte reduktive Cyclisierung von Ketonitrilen
inferred← citeshttps://doi.org/10.1002/ange.201402834openalex-snapshot
Catalytic Asymmetric Synthesis of 8‐Oxabicyclooctanes by Intermolecular [5+2] Pyrylium Cycloadditions
inferred← citeshttps://doi.org/10.1002/ange.202312829openalex-snapshot
Light‐Driven Enantioselective Carbene‐Catalyzed Radical‐Radical Coupling
inferred← citeshttps://doi.org/10.1002/anie.200802203openalex-snapshot
Rapid Construction of the Cortistatin Pentacyclic Core
inferred← citeshttps://doi.org/10.1002/anie.200803550openalex-snapshot
Total Synthesis of (+)‐Cortistatin A
inferred← citeshttps://doi.org/10.1002/anie.200803720openalex-snapshot
Highlights in Steroid Chemistry: Total Synthesis versus Semisynthesis
inferred← citeshttps://doi.org/10.1002/anie.200901116openalex-snapshot
Stereodivergent Synthesis of 17‐α and 17‐β‐Aryl Steroids: Application and Biological Evaluation of D‐Ring Cortistatin Analogues
inferred← citeshttps://doi.org/10.1002/anie.200904565openalex-snapshot
Brønsted Acid Catalyzed Enantioselective Semipinacol Rearrangement for the Synthesis of Chiral Spiroethers
inferred← citeshttps://doi.org/10.1002/anie.200904778openalex-snapshot
Cortistatin A is a High‐Affinity Ligand of Protein Kinases ROCK, CDK8, and CDK11
inferred← citeshttps://doi.org/10.1002/anie.201104769openalex-snapshot
A Versatile Synthesis of Substituted Isoquinolines
inferred← citeshttps://doi.org/10.1002/anie.201202699openalex-snapshot
Asymmetric Syntheses of 8‐Oxabicyclo[3,2,1]octanes: A Cationic Cascade Cyclization
inferred← citeshttps://doi.org/10.1002/anie.201204274openalex-snapshot
Organocatalytic Asymmetric Direct CH Functionalization of Ethers: A Highly Efficient Approach to Chiral Spiroethers
inferred← citeshttps://doi.org/10.1002/anie.201204469openalex-snapshot
Enantioselective Titanium(III)‐Catalyzed Reductive Cyclization of Ketonitriles
inferred← citeshttps://doi.org/10.1002/anie.201402834openalex-snapshot
Catalytic Asymmetric Synthesis of 8‐Oxabicyclooctanes by Intermolecular [5+2] Pyrylium Cycloadditions
inferred← citeshttps://doi.org/10.1002/anie.202312829openalex-snapshot
Light‐Driven Enantioselective Carbene‐Catalyzed Radical‐Radical Coupling
inferred← citeshttps://doi.org/10.1002/asia.202200896openalex-snapshot
Total Synthesis of Natural Products using Gold Catalysis
inferred← citeshttps://doi.org/10.1002/cbdv.202401971openalex-snapshot
Natural Products‐Based Anticancer Agents: Synthesis and Anticancer Activities of Funtumine Amide/Sulfonamide Derivatives
inferred← citeshttps://doi.org/10.1002/cbdv.71504openalex-snapshot
Marine Natural Products From Indonesia and Their Biosynthetic Origins: Part 1: Terpenoids and Meroterpenoids
inferred← citeshttps://doi.org/10.1002/chem.200902185openalex-snapshot
Gold‐Catalyzed Transannular [4+3] Cycloaddition Reactions
inferred← citeshttps://doi.org/10.1002/chem.201502890openalex-snapshot
Formal Total Synthesis of (+)‐Cortistatins A and J
inferred← citeshttps://doi.org/10.1002/chem.201800019openalex-snapshot
Transannular [4+3] Cycloadditions of Macrocyclic Epoxy Ketones
inferred← citeshttps://doi.org/10.1002/chem.201900807openalex-snapshot
Rapid Access to Oxa‐Bridged Bicyclic Skeletons through Gold‐Catalyzed Tandem Rearrangement Reaction
inferred← citeshttps://doi.org/10.1002/chem.202100763openalex-snapshot
Catalytic Reductive Cross‐Coupling between Aromatic Aldehydes and Arylnitriles
inferred← citeshttps://doi.org/10.1002/chem.202104329openalex-snapshot
Vinylcyclopropane [3+2] Cycloaddition with Acetylenic Sulfones Based on Visible Light Photocatalysis**
inferred← citeshttps://doi.org/10.1002/cjoc.201600277openalex-snapshot
Efficient Synthesis of Isoquinolines by AgNO3‐Catalyzed Sequential Imination‐Annulation of 2‐Alkynyl Aldehydes with Ammonium Bicarbonate
inferred← citeshttps://doi.org/10.1002/cmdc.201000302openalex-snapshot
Hypoxia‐Selective Growth Inhibition of Cancer Cells by Furospinosulin‐1, a Furanosesterterpene Isolated from an Indonesian Marine Sponge
inferred← citeshttps://doi.org/10.1002/ejoc.200400567openalex-snapshot
A Formal [3 + 3] Cycloaddition Approach to Natural‐Product Synthesis
inferred← citeshttps://doi.org/10.1002/ejoc.201000247openalex-snapshot
Synthetic Strategies Directed Towards the Cortistatin Family of Natural Products
inferred← citeshttps://doi.org/10.1002/ejoc.201100020openalex-snapshot
Sn(OTf)2 as an Effective Lewis Acid in Reactions of Cyclopropyl Ketones with Acetic Anhydride: Application in the Synthesis of a 19‐Nor‐B‐homo Steroid
inferred← citeshttps://doi.org/10.1002/ejoc.201200162openalex-snapshot
Synthesis of Substituted Furans through Domino Aldol/Homo‐Michael Reactions of Formylcyclopropane 1,1‐Diesters with 1,3‐Dicarbonyls
inferred← citeshttps://doi.org/10.1002/ejoc.201301033openalex-snapshot
The Orthoester Johnson–Claisen Rearrangement in the Synthesis of Bioactive Molecules, Natural Products, and Synthetic Intermediates – Recent Advances
inferred← citeshttps://doi.org/10.1002/ijc.31965openalex-snapshot
Therapeutic value of steroidal alkaloids in cancer: Current trends and future perspectives
inferred← citeshttps://doi.org/10.1002/ijch.201100005openalex-snapshot
Terpenoid‐Alkaloids: Their Biosynthetic Twist of Fate and Total Synthesis
inferred← citeshttps://doi.org/10.1002/med.21346openalex-snapshot
Therapeutic Potential of Steroidal Alkaloids in Cancer and Other Diseases
inferred← citeshttps://doi.org/10.1002/med.22113openalex-snapshot
Harnessing the Power of Natural Products for Targeted Protein Degradation
inferred← citeshttps://doi.org/10.1002/vjch.201960001openalex-snapshot
Highly oxygenated isoprenoid lipids derived from terrestrial and aquatic sources: Origin, structures and biological activities
inferred← citeshttps://doi.org/10.1007/978-1-0716-1579-9_7openalex-snapshot
Designing Efficient Cascade Reactions in Drug Discovery
inferred← citeshttps://doi.org/10.1007/978-1-4614-4654-5_9openalex-snapshot
Natural Products as Tools for Discovering New Cancer Targets
inferred← citeshttps://doi.org/10.1007/978-3-032-01098-8_2openalex-snapshot
Chemical Evolution of Indonesian Marine Natural Products
inferred← citeshttps://doi.org/10.1007/978-3-319-07145-9_3openalex-snapshot
Marine Sponge Derived Antiangiogenic Compounds
inferred← citeshttps://doi.org/10.1007/978-4-431-54038-0_9openalex-snapshot
Search for New Medicinal Seeds from Marine Organisms
inferred← citeshttps://doi.org/10.1007/978-81-322-2794-6_14openalex-snapshot
Marine Sponge-Derived Antiangiogenic Compounds for Cancer Therapeutics
inferred← citeshttps://doi.org/10.1007/978-94-024-1612-1_15openalex-snapshot
Natural Products from Sponges
inferred← citeshttps://doi.org/10.1007/978-981-13-6244-6_12openalex-snapshot
Exploring Bioactive Marine Natural Products and Identification of Their Molecular Targets
inferred← citeshttps://doi.org/10.1007/s00044-025-03486-2openalex-snapshot
Synthesis of simplified didehydro-cortistatin A derivatives as anti-proliferative agents
inferred← citeshttps://doi.org/10.1007/s00706-020-02586-6openalex-snapshot
Applications of Knoevenagel condensation reaction in the total synthesis of natural products
inferred← citeshttps://doi.org/10.1007/s11224-023-02239-4openalex-snapshot
Molecular docking, expounding the regiospecificity, stereoselectivity, and the mechanism of [5+2] cycloaddition reaction between ethereal ether and oxidopyrylium
inferred← citeshttps://doi.org/10.1007/s11306-010-0239-2openalex-snapshot
Metabolic fingerprinting as an indicator of biodiversity: towards understanding inter-specific relationships among Homoscleromorpha sponges
inferred← citeshttps://doi.org/10.1007/s11418-010-0477-7openalex-snapshot
Anti-angiogenic effect of triterpenoidal saponins from Polygala senega
inferred← citeshttps://doi.org/10.1007/s13659-022-00345-0openalex-snapshot
Chemistry and bioactivities of natural steroidal alkaloids
inferred← citeshttps://doi.org/10.1007/s41061-016-0018-2openalex-snapshot
Hydrogen-Atom Transfer Reactions
inferred← citeshttps://doi.org/10.1007/s41061-020-00316-4openalex-snapshot
Alkynoates as Versatile and Powerful Chemical Tools for the Rapid Assembly of Diverse Heterocycles under Transition-Metal Catalysis: Recent Developments and Challenges
inferred← citeshttps://doi.org/10.1007/s41061-025-00508-wopenalex-snapshot
A Review of Approaches Developed for Spiroether Synthesis
inferred← citeshttps://doi.org/10.1016/b978-0-323-95086-2.00021-7openalex-snapshot
Anticancer potentiated bioactive compounds from marine flora
inferred← citeshttps://doi.org/10.1016/b978-0-443-21816-3.00011-7openalex-snapshot
Harnessing the power of traditional Chinese medicine for targeted protein degradation
inferred← citeshttps://doi.org/10.1016/b978-0-443-49144-3.00005-8openalex-snapshot
From evolution to innate role: An overview of triterpenoid saponins and steroidal alkaloids in plant secondary metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-444-59603-1.00003-5openalex-snapshot
Synthesis of Bioactive Natural Products by Propargylic Carboxylic Ester Rearrangements
inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00043-5openalex-snapshot
Marine Invertebrates: Sponges
inferred← citeshttps://doi.org/10.1016/j.antiviral.2018.07.016openalex-snapshot
Natural product-derived compounds in HIV suppression, remission, and eradication strategies
inferred← citeshttps://doi.org/10.1016/j.bbagen.2009.03.011openalex-snapshot
Marine pharmacology in 2005–6: Marine compounds with anthelmintic, antibacterial, anticoagulant, antifungal, anti-inflammatory, antimalarial, antiprotozoal, antituberculosis, and antiviral activities; affecting the cardiovascular, immune and nervous systems, and other miscellaneous mechanisms of…
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103624openalex-snapshot
Binding patterns and structure–activity relationship of CDK8 inhibitors
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106873openalex-snapshot
Indoloquinazoline alkaloids suppress angiogenesis and inhibit metastasis of melanoma cells
inferred← citeshttps://doi.org/10.1016/j.bmc.2007.08.017openalex-snapshot
Structure–activity relationship and biological property of cortistatins, anti-angiogenic spongean steroidal alkaloids
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.12.058openalex-snapshot
Angiogenesis inhibitors identified by cell-based high-throughput screening: Synthesis, structure–activity relationships and biological evaluation of 3-[(E)-styryl]benzamides that specifically inhibit endothelial cell proliferation
inferred← citeshttps://doi.org/10.1016/j.bmc.2017.02.038openalex-snapshot
Design and synthesis of selective CDK8/19 dual inhibitors: Discovery of 4,5-dihydrothieno[3′,4′:3,4]benzo[1,2-d]isothiazole derivatives
inferred← citeshttps://doi.org/10.1016/j.bmc.2020.115461openalex-snapshot
New CDK8 inhibitors as potential anti-leukemic agents – Design, synthesis and biological evaluation
inferred← citeshttps://doi.org/10.1016/j.carres.2014.06.007openalex-snapshot
Highly regio- and diastereoselective, acidic clay supported intramolecular nitrile oxide–alkene cycloaddition on d-ribose derived nitriles: an efficient synthetic route to isoxazoline fused five and six membered carbocycles
inferred← citeshttps://doi.org/10.1016/j.chom.2012.05.016openalex-snapshot
An Analog of the Natural Steroidal Alkaloid Cortistatin A Potently Suppresses Tat-Dependent HIV Transcription
inferred← citeshttps://doi.org/10.1016/j.coviro.2019.07.011openalex-snapshot
Targeting HIV-1 proviral transcription
inferred← citeshttps://doi.org/10.1016/j.ejca.2008.07.001openalex-snapshot
Marine pharmacology in 2005–2006: Antitumour and cytotoxic compounds
inferred← citeshttps://doi.org/10.1016/j.ejmcr.2021.100023openalex-snapshot
A comprehensive review on chemistry and pharmacology of marine bioactives as antimetastatic agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.08.002openalex-snapshot
Synthesis and biological evaluations of new analogs of 2-methoxyestradiol: Inhibitors of tubulin and angiogenesis
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.113043openalex-snapshot
Angel or Devil ? - CDK8 as the new drug target
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113391openalex-snapshot
Discovery of a potent, highly selective, and orally bioavailable inhibitor of CDK8 through a structure-based optimisation
inferred← citeshttps://doi.org/10.1016/j.etap.2013.09.014openalex-snapshot
Antiangiogenic effects of marine sponge derived compounds on cancer
inferred← citeshttps://doi.org/10.1016/j.isci.2024.111244openalex-snapshot
CBP/p300 lysine acetyltransferases inhibit HIV-1 expression in latently infected T cells
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2018.05.018openalex-snapshot
Recent applications of Stille reaction in total synthesis of natural products: An update
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2019.07.016openalex-snapshot
NHC–Au(I) catalyzed enantioselective intramolecular [4+3] cycloaddition of furan propargyl esters
inferred← citeshttps://doi.org/10.1016/j.tet.2007.02.112openalex-snapshot
Cortistatins E, F, G, and H, four novel steroidal alkaloids from marine sponge Corticium simplex
inferred← citeshttps://doi.org/10.1016/j.tet.2009.04.002openalex-snapshot
Stereoselective synthesis of N-heterocycles: application of the asymmetric Cu-catalyzed addition of Et2Zn to functionalized alkyl and aryl imines
inferred← citeshttps://doi.org/10.1016/j.tet.2010.01.030openalex-snapshot
Formal total synthesis of (±)-cortistatin A
inferred← citeshttps://doi.org/10.1016/j.tet.2011.10.026openalex-snapshot
Synthetic studies toward (+)-cortistatin A
inferred← citeshttps://doi.org/10.1016/j.tet.2013.11.065openalex-snapshot
First total synthesis of the marine steroid alkaloid plakinamine B
inferred← citeshttps://doi.org/10.1016/j.tet.2017.01.042openalex-snapshot
Short-step synthesis and structure-activity relationship of cortistatin A analogs
inferred← citeshttps://doi.org/10.1016/j.tet.2017.03.078openalex-snapshot
New bromopyrrole alkaloids from the marine sponge Agelas sp.
inferred← citeshttps://doi.org/10.1016/j.tet.2018.08.011openalex-snapshot
A rearranged seco-steroid with new skeleton and five new abnormal progesteroids from Nodulisporium sp.
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130840openalex-snapshot
Transition states of the gold-catalyzed transannular [4+3] cycloaddition reactions: A computational study
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.05.003openalex-snapshot
Cortistatins J, K, L, novel abeo-9(10-19)-androstane-type steroidal alkaloids with isoquinoline unit, from marine sponge Corticium simplex
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.09.018openalex-snapshot
A concise synthesis of the cortistatin core
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.09.019openalex-snapshot
A novel α,β-unsaturated nitrone-aryne [3+2] cycloaddition and its application in the synthesis of the cortistatin core
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.09.157openalex-snapshot
Synthesis of CD-ring structure of cortistatin A, an anti-angiogenic steroidal alkaloid from marine sponge
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.02.038openalex-snapshot
Efficient and stereoselective installation of isoquinoline: formal total synthesis of cortistatin A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.03.138openalex-snapshot
Gold-catalyzed transannular [4+3] cycloaddition reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.02.099openalex-snapshot
Gold-catalyzed intermolecular [4C+3C] cycloaddition reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.10.043openalex-snapshot
Direct amination of EF spiroketal in steroidal sapogenins: an efficient synthetic strategy and method for related alkaloids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.007openalex-snapshot
Recent application of oxa-Michael reaction in complex natural product synthesis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.01.027openalex-snapshot
Synthetic studies toward swinhoeisterol A, a novel steroid with an unusual carbon skeleton
inferred← citeshttps://doi.org/10.1016/s0959-6380(02)80009-5openalex-snapshot
Chapter 5.3 Five-membered ring systems: Furans and benzofurans
inferred← citeshttps://doi.org/10.1016/s0959-6380(08)80009-8openalex-snapshot
Chapter 5.3 Five-membered ring systems: furans and benzofurans
inferred← citeshttps://doi.org/10.1021/acs.accounts.5c00174openalex-snapshot
Skeletal Editing Strategies Driven by Total Synthesis
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00504openalex-snapshot
Structural Simplification of Natural Products
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01648openalex-snapshot
Straightforward Stereoselective Synthesis of Seven-Membered Oxa-Bridged Rings through In Situ Generated Cycloheptenol Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01391openalex-snapshot
Transition-Metal-Free Direct α-Arylation of Weinreb-type Amides with Arylboronic Acids through Aza-oxyallyl Cation Intermediates
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02206openalex-snapshot
Synthesis of 6-oxa-Spiro[4.5]decane Derivatives by Merging Ring-Opening of Benzo[c]oxepines and Formal 1,2-Oxygen Migration
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00953openalex-snapshot
Diastereoselective Synthesis of CF3- and CF2H-Substituted Spiroethers from Aryl-Fused Cycloalkenylalkanols by Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01133openalex-snapshot
Divergent Synthesis of Solanidine and 22-epi-Solanidine
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01235openalex-snapshot
NHC-Cu(I)-Catalyzed Friedländer-Type Annulation of Fluorinated o-Aminophenones with Alkynes on Water: Competitive Base-Catalyzed Dibenzo[b,f][1,5]diazocine Formation
inferred← citeshttps://doi.org/10.1021/acs.joc.7b03196openalex-snapshot
A Convergent Approach to Diverse Spiroethers through Stereoselective Trapping of Rhodium Carbenoids with Gold-Activated Alkynols
inferred← citeshttps://doi.org/10.1021/acs.joc.8b03249openalex-snapshot
Ti(II) and Rh(I) Complexes as Reagents toward a Thapsigargin Core
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c04075openalex-snapshot
A Water-Soluble 5/14-Carbobicyclic Steroid with a trans-9,11-Epoxy Ring from the Marine Dinoflagellate Amphidinium gibbosum: Insights into Late-Stage Diversification of Steroids
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03384openalex-snapshot
Asymmetric Hydrogenation of Racemic α-Aryl-β-ethoxycarbonyl Cyclopentanones via Dynamic Kinetic Resolution and Its Application to the Synthesis of (+)-Burmaniol A
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02143openalex-snapshot
Electrochemical Promoted Three-Component Trifluoromethylation/Spirocyclization Reaction of N-Arylsulfonylacrylamides to 4-Azaspiro[4.5]decanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c04004openalex-snapshot
Synthesis of Chiral α-Aryl Ketones by Photoredox/Nickel-Catalyzed Enantioconvergent Acyl Cross-Coupling with Organotrifluoroborate
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01048openalex-snapshot
Synthesis of the Cortistatin Pentacyclic Core by Alkoxide-Directed Metallacycle-Mediated Annulative Cross-Coupling
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01320openalex-snapshot
Synthesis of Demissidine and Solanidine
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02561openalex-snapshot
Synthesis of the Pentacyclic Skeleton of Cortistatins
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00834openalex-snapshot
Access to a Guanacastepene and Cortistatin-Related Skeleton via Ethynyl Lactone Ireland–Claisen Rearrangement and Transannular (4 + 3)-Cycloaddition of an Azatrimethylenemethane Diyl
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03196openalex-snapshot
Catalytic Enantioselective Intermolecular [5 + 2] Dipolar Cycloadditions of a 3-Hydroxy-4-pyrone-Derived Oxidopyrylium Ylide
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03461openalex-snapshot
In(OTf)3-Catalyzed Cascade Cyclization for Construction of Oxatricyclic Compounds
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00491openalex-snapshot
Synthesis of Oxa-Bridged Medium-Sized Carbocyclic Rings via Prins Cyclization
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01705openalex-snapshot
Enantioselective, Organocatalytic, Dissymmetric 1,4- and 1,2-Addition of Malononitrile to a Keto-bisenone Followed by an Oxa-Michael Addition Cascade
inferred← citeshttps://doi.org/10.1021/acscatal.0c01495openalex-snapshot
Visible-Light-Promoted Site-Specific and Diverse Functionalization of a C(sp3)–C(sp3) Bond Adjacent to an Arene
inferred← citeshttps://doi.org/10.1021/acscatal.5c06593openalex-snapshot
Divergent Synthesis of Chiral δ-Boryl Ketones via Copper-Catalyzed Carbonylative 1,4-Borylallylation
inferred← citeshttps://doi.org/10.1021/acscatal.6c01939openalex-snapshot
Synthesis of α-(Hetero)aryl Ketones by Ni-Catalyzed Regio- and Enantioselective Hydroacylation of Alkenes with Acid Chlorides
inferred← citeshttps://doi.org/10.1021/acscatal.9b04480openalex-snapshot
Catalytic Enantioselective α-Arylation of Carbonyl Enolates and Related Compounds
inferred← citeshttps://doi.org/10.1021/ar800182ropenalex-snapshot
Chemoselectivity: The Mother of Invention in Total Synthesis
inferred← citeshttps://doi.org/10.1021/cr100376wopenalex-snapshot
Transition Metal Catalyzed Cycloisomerizations of 1, n -Allenynes and -Allenenes
inferred← citeshttps://doi.org/10.1021/cr9002402openalex-snapshot
Novel Syntheses of Bridge-Containing Organic Compounds
inferred← citeshttps://doi.org/10.1021/ja202103eopenalex-snapshot
Scalable Synthesis of Cortistatin A and Related Structures
inferred← citeshttps://doi.org/10.1021/ja206138dopenalex-snapshot
Total Synthesis of (±)-Cortistatin J from Furan
inferred← citeshttps://doi.org/10.1021/ja2105043openalex-snapshot
Asymmetric Synthesis of Dihydroindanes by Convergent Alkoxide-Directed Metallacycle-Mediated Bond Formation
inferred← citeshttps://doi.org/10.1021/ja403824yopenalex-snapshot
TEMPO-catalyzed Aerobic Oxygenation and Nitrogenation of Olefins via C═C Double-Bond Cleavage
inferred← citeshttps://doi.org/10.1021/ja505131vopenalex-snapshot
Design, Development, Mechanistic Elucidation, and Rational Optimization of a Tandem Ireland Claisen/Cope Rearrangement Reaction for Rapid Access to the (Iso)Cyclocitrinol Core
inferred← citeshttps://doi.org/10.1021/ja8071918openalex-snapshot
Enantioselective Synthesis of (+)-Cortistatin A, a Potent and Selective Inhibitor of Endothelial Cell Proliferation
inferred← citeshttps://doi.org/10.1021/ja902601eopenalex-snapshot
Discovery of Potent and Practical Antiangiogenic Agents Inspired by Cortistatin A
inferred← citeshttps://doi.org/10.1021/ja902939topenalex-snapshot
Total Synthesis and Biological Evaluation of Cortistatins A and J and Analogues Thereof
inferred← citeshttps://doi.org/10.1021/jacs.3c00637openalex-snapshot
Stereospecific Acylative Suzuki–Miyaura Cross-Coupling: General Access to Optically Active α-Aryl Carbonyl Compounds
inferred← citeshttps://doi.org/10.1021/jacs.5b09617openalex-snapshot
Correction to “Design, Development, Mechanistic Elucidation, and Rational Optimization of a Tandem Ireland Claisen/Cope Rearrangement Reaction for Rapid Access to the (Iso)Cyclocitrinol Core”
inferred← citeshttps://doi.org/10.1021/jacs.5c03418openalex-snapshot
A Unified Approach to Chiral α-Aryl Ketones and Aldehydes via Ni-Catalyzed Asymmetric Reductive Cross-Coupling
inferred← citeshttps://doi.org/10.1021/jacs.5c03451openalex-snapshot
Nickel-Catalyzed Adaptive Migration-Enabled Asymmetric Cross-Hydrocarbonylation of Unactivated Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.8b02629openalex-snapshot
Asymmetric Total Synthesis of Cyclocitrinol
inferred← citeshttps://doi.org/10.1021/jacsau.6c00311openalex-snapshot
Inductive Diastereoselective Rationale for a Catalytic Strategy to Build Densely Chiral Five-Membered Carbocycles
inferred← citeshttps://doi.org/10.1021/jo101175bopenalex-snapshot
Catalytic Asymmetric Synthesis of the endo-6-Aryl-8-oxabicyclo[3.2.1]oct-3-en-2-one Natural Product from Ligusticum chuanxing via 1,3-Dipolar Cycloaddition of a Formyl-Derived Carbonyl Ylide Using Rh2(S-TCPTTL)4
inferred← citeshttps://doi.org/10.1021/jo2002616openalex-snapshot
Total Synthesis of Cortistatins A and J
inferred← citeshttps://doi.org/10.1021/jo3024973openalex-snapshot
Synthesis of 7-Oxabicyclo[2.2.1]heptanes and 8-Oxabicyclo[3.2.1]octanes from C-Glycosides via an Intramolecular Cyclization
inferred← citeshttps://doi.org/10.1021/ml300143dopenalex-snapshot
Creation of Readily Accessible and Orally Active Analogue of Cortistatin A
inferred← citeshttps://doi.org/10.1021/np060489vopenalex-snapshot
Halogenated Cyclic Peptides Isolated from the Sponge Corticium sp.
inferred← citeshttps://doi.org/10.1021/np070165mopenalex-snapshot
Variation in Cytostatic Constituents of a Sponge-Derived Gymnascella dankaliensis by Manipulating the Carbon Source
inferred← citeshttps://doi.org/10.1021/np500556topenalex-snapshot
Steroidal Alkaloids from the Marine Sponge Corticium niger That Inhibit Growth of Human Colon Carcinoma Cells
inferred← citeshttps://doi.org/10.1021/ol102058fopenalex-snapshot
Concise Synthesis of the Oxapentacyclic Core of Cortistatin A
inferred← citeshttps://doi.org/10.1021/ol102798fopenalex-snapshot
Enantioselective Synthesis of 2,2,5-Tri- and 2,2,5,5-Tetrasubstituted Tetrahydrofurans via [4 + 2] Cycloaddition and Ring-Opening Cross-Metathesis
inferred← citeshttps://doi.org/10.1021/ol201327uopenalex-snapshot
Stereoselective Synthesis of Core Structure of Cortistatin A
inferred← citeshttps://doi.org/10.1021/ol301532wopenalex-snapshot
Synthesis of B-Ring-Modified Steroids through BF3-Promoted Rearrangement/Substitution of 6β-Hydroxy-5,19-cyclosteroids
inferred← citeshttps://doi.org/10.1021/ol401235zopenalex-snapshot
Double Hetero-Michael Addition of N -Substituted Hydroxylamines to Quinone Monoketals: Synthesis of Bridged Isoxazolidines
inferred← citeshttps://doi.org/10.1021/ol702325eopenalex-snapshot
Amaranzole A, a New N-Imidazolyl Steroid from Phorbas amaranthus
inferred← citeshttps://doi.org/10.1021/ol8012099openalex-snapshot
A Concise Synthesis of the Pentacyclic Framework of Cortistatins
inferred← citeshttps://doi.org/10.1021/ol802328nopenalex-snapshot
A Short, Scalable Synthesis of the Carbocyclic Core of the Anti-Angiogenic Cortistatins from (+)-Estrone by B-Ring Expansion
inferred← citeshttps://doi.org/10.1021/ol901537nopenalex-snapshot
Intramolecular Cyclopropene-Furan [2 + 4] Cycloaddition followed by a Cyclopropylcarbinyl Rearrangement to Synthesize the BCD Rings of Cortistatin A
inferred← citeshttps://doi.org/10.1021/ol902168gopenalex-snapshot
A Hypervalent Iodine-Induced Double Annulation Enables a Concise Synthesis of the Pentacyclic Core Structure of the Cortistatins
inferred← citeshttps://doi.org/10.1038/nchem.794openalex-snapshot
Synthesis of cortistatins A, J, K and L
inferred← citeshttps://doi.org/10.1038/ncomms9617openalex-snapshot
Towards a general diastereoselective route to oxabicyclo[3.2.1]octanes via a gold-catalysed cascade reaction
inferred← citeshttps://doi.org/10.1038/s41467-025-57967-4openalex-snapshot
Rapid assembly of enantioenriched α-arylated ketones via Ni-catalyzed asymmetric cross-hydrocarbonylation enabled by alkene sorting
inferred← citeshttps://doi.org/10.1038/srep29744openalex-snapshot
Involucratusins A–H: Unusual Cadinane Dimers from Stahlianthus involucratus with Multidrug Resistance Reversal Activity
inferred← citeshttps://doi.org/10.1039/9781788016131-00343openalex-snapshot
Transition Metal-catalysed Nucleophilic Additions of Terminal Alkynes in Water: Development and Synthetic Utility
inferred← citeshttps://doi.org/10.1039/b602241nopenalex-snapshot
The value of natural products to future pharmaceutical discovery
inferred← citeshttps://doi.org/10.1039/b701533jopenalex-snapshot
Marine natural products: synthetic aspects
showing the first 200 of 292 · page through all 292
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.