On the public citation graph

Total synthesis of (.+-.)-paeoniflorigenin and paeoniflorin

https://doi.org/10.1021/ja00072a063
0 signed · 85 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4581501openalex-extracted
A New Strategy for Coupling Amides or Nitriles with Diarylketones Promoted by Samarium Metal Under the Catalysis of Cui
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(20000103)112:1<46::aid-ange46>3.0.co;2-popenalex-snapshot
Der Stand der Totalsynthese zu Beginn des 21. Jahrhunderts
inferred← citeshttps://doi.org/10.1002/0471264180.or049.03openalex-snapshot
Carbon–Carbon Bond‐Forming Reactions Promoted by Trivalent Manganese
inferred← citeshttps://doi.org/10.1002/9780470053485.ch2openalex-snapshot
Protection for the Hydroxyl Group, Including 1,2‐ and 1,3‐Diols
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0131openalex-snapshot
Some Synthetic Uses of Double‐Bonded Functional Groups
inferred← citeshttps://doi.org/10.1002/9781118662083.cot04-011openalex-snapshot
Halogenation of Carbonyl and Related Compounds
inferred← citeshttps://doi.org/10.1002/9781118662083.cot09-008openalex-snapshot
Lactone and Lactam Formation
inferred← citeshttps://doi.org/10.1002/9781118905074.ch02openalex-snapshot
Protection for the Hydroxyl Group, Including 1,2‐ and 1,3‐Diols
inferred← citeshttps://doi.org/10.1002/9781118940228.ch4openalex-snapshot
Organometallics‐Based Catalytic (Asymmetric) Synthesis of Natural Products
inferred← citeshttps://doi.org/10.1002/9781118940228.ch6openalex-snapshot
Recent Applications of Kagan's Reagent (SmI2) in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1002/9781119953678.rad037openalex-snapshot
Manganese(III) Acetate, CAN , and Fe (III) Salts in Oxidative Radical Chemistry
inferred← citeshttps://doi.org/10.1002/9783527618255.ch5openalex-snapshot
Glycosylation Methods: Use of Phosphites
inferred← citeshttps://doi.org/10.1002/9783527618293.ch11openalex-snapshot
Manganese(III)‐Mediated Radical Reactions
inferred← citeshttps://doi.org/10.1002/9783527618293.ch41openalex-snapshot
Synthesis of Oxacyclic Natural Products
inferred← citeshttps://doi.org/10.1002/9783527621644.ch3bopenalex-snapshot
Glycoside Synthesis from 1‐Oxygen Substituted Glycosyl Donors: Sections 3.3 and 3.4
inferred← citeshttps://doi.org/10.1002/9783527675142.ch18openalex-snapshot
Si–C – X and Si–C – EWG as Carbanion Equivalents under Lewis Base Activation ( n ?→?σ*)
inferred← citeshttps://doi.org/10.1002/ange.19951070505openalex-snapshot
Enzyme in der organischen Synthese: das Problem der molekularen Erkennung von Kohlenhydraten (Teil 2)
inferred← citeshttps://doi.org/10.1002/ange.201106889openalex-snapshot
Totalsynthese von (+)‐Lactiflorin durch intramolekulare [2+2]‐Photocycloaddition
inferred← citeshttps://doi.org/10.1002/anie.199505211openalex-snapshot
Enzymes in Organic Synthesis: Application to the Problems of Carbohydrate Recognition (Part 2)
inferred← citeshttps://doi.org/10.1002/anie.201106889openalex-snapshot
Total Synthesis of (+)‐Lactiflorin by an Intramolecular [2+2] Photocycloaddition
inferred← citeshttps://doi.org/10.1002/chem.200401163openalex-snapshot
Photoinduced Electron Transfer Reactions by SmI2 in THF: Luminescence Quenching Studies and Mechanistic Investigations
inferred← citeshttps://doi.org/10.1002/chem.201705575openalex-snapshot
Total Synthesis of Sarpagine‐Related Bioactive Indole Alkaloids
inferred← citeshttps://doi.org/10.1002/chin.199404215openalex-snapshot
ChemInform Abstract: Total Synthesis of (.+‐.)‐Paeoniflorigenin and Paeoniflorin.
inferred← citeshttps://doi.org/10.1002/chin.200352091openalex-snapshot
Direct Catalytic Aldol‐Type Reactions Using RCH2CN.
inferred← citeshttps://doi.org/10.1002/ejoc.200700397openalex-snapshot
In Pursuit of cis,cis,cis‐Cyclonona‐2,5,8‐triene‐1,4,7‐trione – An Adventure in Medium‐Sized Ring Chemistry
inferred← citeshttps://doi.org/10.1002/ejoc.200900527openalex-snapshot
Reaction of the Electrogenerated Cyanomethyl Anion with Carbonyl Compounds: A Clean and Safe Synthesis of β‐Hydroxynitriles
inferred← citeshttps://doi.org/10.1002/ejoc.202400474openalex-snapshot
Brønsted Acid Catalyzed Dehydroxylative Cyanation of Benzylic Alcohols with Trimethylsilyl Cyanide Using 1,1,1,3,3,3‐Hexafluoro‐2‐propanol as a Solvent
inferred← citeshttps://doi.org/10.1002/prac.19973390189openalex-snapshot
Manganese(III) acetate - A Versatile Reagent for Radical Generation and CC Bond Formation
inferred← citeshttps://doi.org/10.1007/3418_2015_135openalex-snapshot
Recent Advances on the Chemistry of POCOP–Nickel Pincer Compounds
inferred← citeshttps://doi.org/10.1007/978-3-031-42422-9_1openalex-snapshot
Neurotrophic Natural Products
inferred← citeshttps://doi.org/10.1007/s11101-017-9527-zopenalex-snapshot
Neuroprotective effects of paeoniflorin in neurodegenerative diseases of the central nervous system
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00793-8openalex-snapshot
Monoterpene and coumarin glucosides of Cnidium silaifolium
inferred← citeshttps://doi.org/10.1016/0040-4020(95)00434-aopenalex-snapshot
Redox induced radical and radical ionic carbon-carbon bond forming reactions
inferred← citeshttps://doi.org/10.1016/0040-4039(95)00263-copenalex-snapshot
An extremely mild and stereocontrolled construction of 1,2-trans-β-glycosidic linkages capitalizing on benzyl-protected glycopyranosyl diethyl phosphites as glycosyl donors
inferred← citeshttps://doi.org/10.1016/0040-4039(95)00938-9openalex-snapshot
Synthesis of optically active trans-cyclononenes A possible approach to xenicanes
inferred← citeshttps://doi.org/10.1016/0040-4039(95)01913-3openalex-snapshot
Studies in macrolide synthesis: A sequential aldol/glycosylation approach to the synthesis of concanamycin A
inferred← citeshttps://doi.org/10.1016/b978-0-12-817903-1.00001-2openalex-snapshot
The C-19 methyl substituted sarpagine-macroline-ajmaline alkaloids: Diversity, occurrence, bioactivity, and synthesis
inferred← citeshttps://doi.org/10.1016/b978-0-615-39515-9.50008-4openalex-snapshot
Examples of Enantioselective Synthesis
inferred← citeshttps://doi.org/10.1016/b978-012651645-6/50004-4openalex-snapshot
Hydrogenolysis
inferred← citeshttps://doi.org/10.1016/j.catcom.2012.03.021openalex-snapshot
Choline chloride based eutectic solvents: Magical catalytic system for carbon–carbon bond formation in the rapid synthesis of β-hydroxy functionalized derivatives
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.03.014openalex-snapshot
Synthetic approaches to access acortatarins, shensongines and pollenopyrroside; potent antioxidative spiro-alkaloids with a naturally rare morpholine moiety
inferred← citeshttps://doi.org/10.1016/j.molliq.2022.121013openalex-snapshot
Deep eutectic solvents as reusable catalysts and promoter for the greener syntheses of small molecules: Recent advances
inferred← citeshttps://doi.org/10.1016/j.tet.2006.02.014openalex-snapshot
Studies in stereoselective [2+2]-cycloadditions with dichloroketene
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.02.080openalex-snapshot
N-Heterocyclic carbene-catalyzed cyanomethylation of aldehydes with TMSAN
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154819openalex-snapshot
A new strategy for coupling amides or nitriles with diarylketones promoted by samarium metal under the catalysis of CuI
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)89683-6openalex-snapshot
Glycosylation using glycosyl phosphite as a glycosyl donor
inferred← citeshttps://doi.org/10.1016/s0040-4020(96)01038-1openalex-snapshot
Synthesis of 2,6-di-O-α-D-mannopyranosylphosphatidyl-D-myo-inositol. Utilization of glycosylation and phosphorylation based on phosphite chemistry
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)00348-8openalex-snapshot
SmI2-mediated nitrile aldol reaction
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)76961-9openalex-snapshot
Utility of glycosyl phosphites as glycosyl donors-fructofuranosyl and 2-deoxyhexopyranosyl phosphites in glycoside bond formation
inferred← citeshttps://doi.org/10.1016/s0040-4039(97)01418-4openalex-snapshot
GLYCOSYL DONORS WITH PHOSPHORIMIDATE LEAVING GROUPS FOR EITHER α- OR β- GLYCOSIDATION
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00833openalex-snapshot
Methods Utilizing First-Row Transition Metals in Natural Product Total Synthesis
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00834openalex-snapshot
Navigating the Chiral Pool in the Total Synthesis of Complex Terpene Natural Products
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00144openalex-snapshot
Catalytic Glycosylations in Oligosaccharide Synthesis
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.1c00790openalex-snapshot
Geminal Diheteroatomic Motifs: Some Applications of Acetals, Ketals, and Their Sulfur and Nitrogen Homologues in Medicinal Chemistry and Drug Design
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00054openalex-snapshot
Mn-Mediated α-Radical Addition of Carbonyls to Olefins: Systematic Study, Scope, and Electrocatalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00080openalex-snapshot
Synthetic Access Toward Cycloastragenol Glycosides
inferred← citeshttps://doi.org/10.1021/cr030017aopenalex-snapshot
Samarium(II)-Iodide-Mediated Cyclizations in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1021/cr950019yopenalex-snapshot
Sequencing Reactions with Samarium(II) Iodide
inferred← citeshttps://doi.org/10.1021/cr980326eopenalex-snapshot
Coupling of Organic Halides with Carbonyl Compounds Promoted by SmI2, the Kagan Reagent
inferred← citeshttps://doi.org/10.1021/ja020051ropenalex-snapshot
Mechanistic Study of β-Substituent Effects on the Mechanism of Ketone Reduction by SmI2
inferred← citeshttps://doi.org/10.1021/ja407827nopenalex-snapshot
Total Synthesis of Vineomycin B2
inferred← citeshttps://doi.org/10.1021/ja807613qopenalex-snapshot
Key Role of Ti(IV) in the Selective Radical−Radical Cross-Coupling Mediated by the Ingold-Fischer Effect
inferred← citeshttps://doi.org/10.1021/ja952265xopenalex-snapshot
Synthesis of Sialyl Lewis X Mimetics and Related Structures Using the Glycosyl Phosphite Methodology and Evaluation of E-Selectin Inhibition
inferred← citeshttps://doi.org/10.1021/jacs.5c00855openalex-snapshot
Pd-Catalyzed Counter-Steric Site- and Chemoselective Glycosylation: Total Synthesis of Fridamycin A and Himalomycin B
inferred← citeshttps://doi.org/10.1021/jo8026033openalex-snapshot
Ti(III)-Promoted Radical Cyclization of Epoxy Enones. Total Synthesis of (+)-Paeonisuffrone
inferred← citeshttps://doi.org/10.1021/jo900814topenalex-snapshot
P(i-PrNCH2CH2)3N as a Lewis Base Catalyst for the Synthesis of β-Hydroxynitriles Using TMSAN
inferred← citeshttps://doi.org/10.1021/ol035206uopenalex-snapshot
Direct Catalytic Aldol-Type Reactions Using RCH2CN
inferred← citeshttps://doi.org/10.1021/ol102446uopenalex-snapshot
Toward the Total Synthesis of Maoecrystal V: Establishment of Contiguous Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1039/9781839169052-00658openalex-snapshot
Applications of Conventional Free Radicals and Advances in Total Synthesis: from the Bench to Nature through SmI2 Radicals as an Efficient Trigger for Radical Cascades, a Journey from Orsay to the 21st Century*
inferred← citeshttps://doi.org/10.1039/b001386mopenalex-snapshot
Synthesis of adenophostin A and congeners modified at glucose
inferred← citeshttps://doi.org/10.1039/c5ob01560jopenalex-snapshot
An efficient aldol-type direct reaction of isatins with TMSCH 2 CN
inferred← citeshttps://doi.org/10.1039/c7np00065kopenalex-snapshot
Total synthesis of complex terpenoids employing radical cascade processes
inferred← citeshttps://doi.org/10.1039/d0qo00024hopenalex-snapshot
Cu 2 O-catalyzed selective 1,2-addition of acetonitrile to α,β-unsaturated aldehydes
inferred← citeshttps://doi.org/10.1039/d6ra01217eopenalex-snapshot
Selective 1,2-addition of acetonitrile/acetone to α,β-unsaturated aldehydes at room temperature: access to cinnamyl alcohol derivatives with potential protective effects against exercise-induced skeletal muscle injury
inferred← citeshttps://doi.org/10.1055/a-1654-2211openalex-snapshot
Trimethylsilyl Esters as Novel Dual-Purpose Protecting Reagents
inferred← citeshttps://doi.org/10.1055/s-0040-1720837openalex-snapshot
Synthesis of (±)-Paeoniflorigenin
inferred← citeshttps://doi.org/10.1080/00304948.2021.1877238openalex-snapshot
N,O-Benzyl Protection of Structurally Varied Amines and Phenols Using Wells-Dawson Heteropolyacid Catalyst
inferred← citeshttps://doi.org/10.1093/femsle/fny263openalex-snapshot
Diversity of endophytic fungi of Paeonia lactiflora Pallas and screening for fungal paeoniflorin producers
inferred← citeshttps://doi.org/10.1111/ics.12309openalex-snapshot
The skin‐depigmenting potential of Paeonia lactiflora root extract and paeoniflorin: in vitro evaluation using reconstructed pigmented human epidermis
inferred← citeshttps://doi.org/10.1177/1934578x19876409openalex-snapshot
The Anticancer Effects of Paeoniflorin and Its Underlying Mechanisms
inferred← citeshttps://doi.org/10.1201/9781420027952.ch4openalex-snapshot
Glycosylation Methods
inferred← citeshttps://doi.org/10.3184/174751914x13888556743823openalex-snapshot
Zinc-mediated Addition of Bromoacetonitrile to Carbonyl Compounds under Solvent-free Conditions
inferred← citeshttps://doi.org/10.3389/fpls.2022.980854openalex-snapshot
Paeoniflorin in Paeoniaceae: Distribution, influencing factors, and biosynthesis
inferred← citeshttps://doi.org/10.3390/molecules29102264openalex-snapshot
Recent Advances in Manganese(III)-Assisted Radical Cyclization for the Synthesis of Natural Products: A Comprehensive Review
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.78.986openalex-snapshot
Fascinated by Natural Product Synthesis
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.