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The Halichondrins and E7389
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.196909811openalex-snapshot
N,N‐Dimethyl‐4‐pyridinamine, a Very Effective Acylation Catalyst
inferredcites →https://doi.org/10.1002/anie.199202281openalex-snapshot
Asymmetric Ligands for Transition‐Metal‐Catalyzed Reactions: 2‐Diphenylphosphinobenzoyl Derivatives of C2‐Symmetric Diols and Diamines
inferredcites →https://doi.org/10.1002/anie.200806111openalex-snapshot
A Total Synthesis of Norhalichondrin B
inferredcites →https://doi.org/10.1002/cber.19751080533openalex-snapshot
Intramolekulare Konkurrenzreaktionen bei der Ozonolyse substituierter Cyclopentene
inferredcites →https://doi.org/10.1002/recl.19750940902openalex-snapshot
Addition of phenols and alcohols to ethoxyethyne Formation of orthoacetates or ketene acetals
inferredcites →https://doi.org/10.1002/recl.19851041005openalex-snapshot
Vitamin‐C‐ and isovitamin‐C‐derived chemistry. Part I. Synthesis of 2,3‐dideoxy derivatives of the Ascorbic acids
inferredcites →https://doi.org/10.1016/0040-4020(78)80197-5openalex-snapshot
Oxidation of alcohols by “activated” dimethyl sulfoxide. a preparative, steric and mechanistic study
inferredcites →https://doi.org/10.1016/0040-4020(84)80008-3openalex-snapshot
On stereochemistry of osmium tetraoxide oxidation of allylic alcohol systems. Empirical rule
inferredcites →https://doi.org/10.1016/0040-4020(89)80064-xopenalex-snapshot
Chlorosilane-accelerated conjugate addition of catalytic and stoichiometric organocopper reagents
inferredcites →https://doi.org/10.1016/0040-4039(91)80600-bopenalex-snapshot
Synthesis of a C(22)a˚C(34) halichondrin precursor via a double dioxanone-to-dihydropyran rearrangement
inferredcites →https://doi.org/10.1016/0040-4039(95)01454-popenalex-snapshot
Enantioselective synthesis of a halichondrin B C(20)→C(36) precursor
inferredcites →https://doi.org/10.1016/j.bmcl.2004.08.068openalex-snapshot
Structurally simplified macrolactone analogues of halichondrin B
inferredcites →https://doi.org/10.1016/j.tetlet.2007.10.116openalex-snapshot
Effective procedure for selective ammonolysis of monosubstituted oxiranes: application to E7389 synthesis
inferredcites →https://doi.org/10.1016/j.tetlet.2008.03.018openalex-snapshot
A synthesis of the C1–C15 domain of the halichondrins
inferredcites →https://doi.org/10.1016/s0021-9258(18)98491-7openalex-snapshot
Halichondrin B and homohalichondrin B, marine natural products binding in the vinca domain of tubulin. Discovery of tubulin-based mechanism of action by analysis of differential cytotoxicity data
inferredcites →https://doi.org/10.1016/s0040-4020(01)92187-8openalex-snapshot
A revised mechanism for chemoselective reduction of esters with borane-dimethyl sulfide complex and catalytic sodium tetrahydroborate directed by adjacent hydroxyl group
inferredcites →https://doi.org/10.1016/s0040-4020(01)97963-3openalex-snapshot
Oxidation of α,β-un saturated aldehydes
inferredcites →https://doi.org/10.1016/s0040-4020(02)00050-9openalex-snapshot
Halichondrin B: synthesis of the C(37)–C(54) subunit
inferredcites →https://doi.org/10.1016/s0040-4039(00)60394-5openalex-snapshot
Synthetic studies on halichondrins: A new practical synthesis of the C.1–C.12 segment
inferredcites →https://doi.org/10.1016/s0040-4039(00)61388-6openalex-snapshot
Total synthesis of halichondrin b from common sugars: An F-ring intermediate from D-glucose and efficient construction of the C1 to C21 segment
inferredcites →https://doi.org/10.1016/s0040-4039(00)73673-2openalex-snapshot
Total synthesis of halichondrins: Enantioselective construction of a homochiral tetracyclic KLMN-ring intermediate from D-mannitol
inferredcites →https://doi.org/10.1016/s0040-4039(00)75204-xopenalex-snapshot
Pyridinium chlorochromate. An efficient reagent for oxidation of primary and secondary alcohols to carbonyl compounds
inferredcites →https://doi.org/10.1016/s0040-4039(00)75795-9openalex-snapshot
An expeditious synthesis of the C(1)-C(14) subunit of halichondrin B
inferredcites →https://doi.org/10.1016/s0040-4039(00)78563-7openalex-snapshot
Isohomohalichondrin B, a new antitumour polyether macrolide from the New Zealand deep-water sponge Lissodendoryx sp.
inferredcites →https://doi.org/10.1016/s0040-4039(00)81416-1openalex-snapshot
An efficient method for the alkynylation of oxiranes using alkynyl boranes
inferredcites →https://doi.org/10.1016/s0040-4039(00)81710-4openalex-snapshot
An improved method for the synthesis of anomerically allylated C-glycopyranosides and C-glycofuranosides.
inferredcites →https://doi.org/10.1016/s0040-4039(00)82884-1openalex-snapshot
Stereoselective reduction of β-alkoxy ketones: a synthesis of syn-1,3-diols
inferredcites →https://doi.org/10.1016/s0040-4039(00)85909-2openalex-snapshot
Direct synthesis of Z-unsaturated esters. A useful modification of the horner-emmons olefination.
inferredcites →https://doi.org/10.1016/s0040-4039(00)86974-9openalex-snapshot
Specific removal of o-methoxybenzyl protection by DDQ oxidation.
inferredcites →https://doi.org/10.1016/s0040-4039(00)87729-1openalex-snapshot
Ozonolytic cleavage of cycloalkenes to terminally differentiated products
inferredcites →https://doi.org/10.1016/s0040-4039(00)88231-3openalex-snapshot
On stereochemistry of osmium tetroxide oxidation of allylic alcohol systems: empirical rule
inferredcites →https://doi.org/10.1016/s0040-4039(00)88417-8openalex-snapshot
Selective grignard-type carbonyl addition of alkenyl halides mediated by chromium(II) chloride
inferredcites →https://doi.org/10.1016/s0040-4039(00)91671-xopenalex-snapshot
Synthetic Studies towards Halichondrins: Synthesis of the C.27–C.38 Segment
inferredcites →https://doi.org/10.1016/s0040-4039(00)91672-1openalex-snapshot
Synthetic Studies Towards Halichondrins: Synthesis of the Left Half of Halichondrins
inferredcites →https://doi.org/10.1016/s0040-4039(00)91673-3openalex-snapshot
Synthetic Studies Towards Halichondrins: Synthesis of the Left Halves of Norhalichondrins and Homohalichondrins
inferredcites →https://doi.org/10.1016/s0040-4039(00)91877-xopenalex-snapshot
Tin(II) chloride catalyzed addition of diazo sulfones, diazo phosphine oxides, and diazo phosphonates to aldehydes.
inferredcites →https://doi.org/10.1016/s0040-4039(00)95673-9openalex-snapshot
1,3- diastereoselective reduction of β-hydroxyketones utilizing alkoxydialkylboranes
inferredcites →https://doi.org/10.1016/s0040-4039(00)96327-5openalex-snapshot
Synthetic studies towards halichondrins
inferredcites →https://doi.org/10.1016/s0040-4039(00)97476-8openalex-snapshot
Total synthesis of halichondrins: Enantioselective construction of a homochiral pentacyclic C1-C15 intermediate from d-ribose
inferredcites →https://doi.org/10.1016/s0040-4039(00)98529-0openalex-snapshot
Stereoselective synthesis of α- C-allyl-glycopyranosides
inferredcites →https://doi.org/10.1016/s0040-4039(01)80205-7openalex-snapshot
Horner-wadsworth-emmons reaction: Use of lithium chloride and an amine for base-sensitive compounds
inferredcites →https://doi.org/10.1016/s0040-4039(01)80261-6openalex-snapshot
Highly stereoselective c-allylation of glycopyranosides with allylsilanes catalyzed by silyl triflate or iodosilane
inferredcites →https://doi.org/10.1016/s0040-4039(01)80274-4openalex-snapshot
Cyclic sulfates containing acid-sensitive groups and chemoselective hydrolysis of sulfate esters
inferredcites →https://doi.org/10.1016/s0040-4039(01)80649-3openalex-snapshot
Synthesis and crystallographic analysis of a bicyclic core related to the esperamicin/calichemicin aglycones
inferredcites →https://doi.org/10.1016/s0040-4039(01)91443-1openalex-snapshot
One-step conversion of protected lactols into lactones
inferredcites →https://doi.org/10.1016/s0040-4039(01)93872-9openalex-snapshot
Total synthesis of halichondrins: Highly stereoselective construction of a homochiral pentasubstituted H-ring pyran intermediate from α-d-glucose
inferredcites →https://doi.org/10.1016/s0040-4039(96)01999-5openalex-snapshot
Synthetic studies on halichondrins: A practical synthesis of the C.1C.13 segment
inferredcites →https://doi.org/10.1016/s0040-4039(97)01462-7openalex-snapshot
Ni(II)/Cr(II)-Mediated Coupling Reaction: Beneficial Effects of 4-tert-Butylpyridine as an Additive and Development of New and Improved Workup Procedures
inferredcites →https://doi.org/10.1016/s0040-4039(97)10364-1openalex-snapshot
Synthetic studies of halichondrin B, an antitumor polyether macrolide isolated from a marine sponge. 8. Synthesis of the lactone part (C1C36) via horner-emmons coupling between C1C15 and C16C36 fragments and Yamaguchi lactonization
inferredcites →https://doi.org/10.1016/s0040-4039(99)00956-9openalex-snapshot
Selective oxidation of primary silyl ethers and its application to the synthesis of natural products
inferredcites →https://doi.org/10.1016/s0960-894x(00)00150-5openalex-snapshot
Structure–activity relationships of Halichondrin B analogues: modifications at C.30–C.38
inferredcites →https://doi.org/10.1021/cr00032a009openalex-snapshot
Catalytic Asymmetric Dihydroxylation
inferredcites →https://doi.org/10.1021/cr00038a012openalex-snapshot
Total Synthesis of Bioactive Marine Macrolides
inferredcites →https://doi.org/10.1021/ja00019a027openalex-snapshot
A useful 12-I-5 triacetoxyperiodinane (the Dess-Martin periodinane) for the selective oxidation of primary or secondary alcohols and a variety of related 12-I-5 species
inferredcites →https://doi.org/10.1021/ja00034a086openalex-snapshot
Total synthesis of halichondrin B and norhalichondrin B
inferredcites →https://doi.org/10.1021/ja00185a050openalex-snapshot
A mechanistic insight leads to a greatly improved osmium-catalyzed asymmetric dihydroxylation process
inferredcites →https://doi.org/10.1021/ja00209a048openalex-snapshot
Selective hydride-mediated conjugate reduction of .alpha.,.beta.-unsaturated carbonyl compounds using [(Ph3P)CuH]6
inferredcites →https://doi.org/10.1021/ja00214a053openalex-snapshot
Asymmetric dihydroxylation via ligand-accelerated catalysis
inferredcites →https://doi.org/10.1021/ja00230a045openalex-snapshot
Vicinal diol cyclic sulfates. Like epoxides only more reactive
inferredcites →https://doi.org/10.1021/ja00252a056openalex-snapshot
Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications
inferredcites →https://doi.org/10.1021/ja00253a032openalex-snapshot
Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization
inferredcites →https://doi.org/10.1021/ja00259a075openalex-snapshot
A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep syntheses
inferredcites →https://doi.org/10.1021/ja00278a057openalex-snapshot
Catalytic effect of nickel(II) chloride and palladium(II) acetate on chromium(II)-mediated coupling reaction of iodo olefins with aldehydes
inferredcites →https://doi.org/10.1021/ja00279a076openalex-snapshot
Intramolecular generation and [2,3]-sigmatropic rearrangement of oxonium ylides
inferredcites →https://doi.org/10.1021/ja00279a077openalex-snapshot
Generation and rearrangements of oxonium ylides
inferredcites →https://doi.org/10.1021/ja00302a042openalex-snapshot
Norhalichondrin A: an antitumor polyether macrolide from a marine sponge
inferredcites →https://doi.org/10.1021/ja00370a050openalex-snapshot
Asymmetric alkylation reactions of chiral imide enolates. A practical approach to the enantioselective synthesis of .alpha.-substituted carboxylic acid derivatives
inferredcites →https://doi.org/10.1021/ja00382a053openalex-snapshot
Highly stereoselective approaches to .alpha.- and .beta.-C-glycopyranosides
inferredcites →https://doi.org/10.1021/ja00399a082openalex-snapshot
Okadaic acid, a cytotoxic polyether from two marine sponges of the genus Halichondria
inferredcites →https://doi.org/10.1021/ja00799a061openalex-snapshot
High stereo- and regioselectivities in the transition metal catalyzed epoxidations of olefinic alcohols by tert-butyl hydroperoxide
inferredcites →https://doi.org/10.1021/ja00823a042openalex-snapshot
Stereoselective epoxidations of acyclic allylic alcohols by transition metal-hydroperoxide reagents. Synthesis of dl-C18 Cecropia juvenile hormone from farnesol
inferredcites →https://doi.org/10.1021/ja01500a050openalex-snapshot
The Partial Synthesis of 12α-Methyl-11-dehydrocorticosterone
inferredcites →https://doi.org/10.1021/ja045557jopenalex-snapshot
Fe/Cr- and Co/Cr-Mediated Catalytic Asymmetric 2-Haloallylations of Aldehydes
inferredcites →https://doi.org/10.1021/ja047826bopenalex-snapshot
A Simple but Remarkably Effective Device for Forming the C8−C14 Polycyclic Ring System of Halichondrin B
inferredcites →https://doi.org/10.1021/ja055966vopenalex-snapshot
Catalytic Ni/Cr-Mediated Macrocyclization without Use of High-Dilution Techniques
inferredcites →https://doi.org/10.1021/ja9537538openalex-snapshot
A Multicomponent Redox System Accounts for the First Nozaki−Hiyama−Kishi Reactions Catalytic in Chromium
inferredcites →https://doi.org/10.1021/ja962081yopenalex-snapshot
Asymmetric Synthesis of Highly Functionalized 8-Oxabicyclo[3.2.1]octene Derivatives
inferredcites →https://doi.org/10.1021/ja9625236openalex-snapshot
Nozaki−Hiyama−Kishi Reactions Catalytic in Chromium
inferredcites →https://doi.org/10.1021/jm00115a027openalex-snapshot
Antineoplastic agents. 219. Isolation and structure of the cell growth inhibitory constituents from the western Pacific marine sponge Axinella sp
inferredcites →https://doi.org/10.1021/jo000140ropenalex-snapshot
Halichondrin B: Synthesis of the C(1)−C(15) Subunit
inferredcites →https://doi.org/10.1021/jo00061a030openalex-snapshot
: Isolation and structure of halistatin 1 from the eastern Indian Ocean marine sponge Phakellia carteri
inferredcites →https://doi.org/10.1021/jo00170a070openalex-snapshot
Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones
inferredcites →https://doi.org/10.1021/jo00189a046openalex-snapshot
Synthesis of amphotericin B. 1. Fragment A of the aglycon
inferredcites →https://doi.org/10.1021/jo00242a054openalex-snapshot
Preparation of optically active 2-furylcarbinols by kinetic resolution using the Sharpless reagent
inferredcites →https://doi.org/10.1021/jo00265a055openalex-snapshot
Preparation of optically active 2-thienylcarbinols by kinetic resolution using the Sharpless reagent
inferredcites →https://doi.org/10.1021/jo00346a050openalex-snapshot
Total synthesis of carbohydrates: stereoselective syntheses of 2,6-dideoxy-D-arabino-hexose and 2,6-dideoxy-D-ribo-hexose
inferredcites →https://doi.org/10.1021/jo00370a005openalex-snapshot
.alpha.-Chelation controlled nucleophilic addition to chiral .alpha.,.beta.-dialkoxy carbonyl compounds. Diastereoselective preparation of L-xylo and L-lyxo triols
inferredcites →https://doi.org/10.1021/jo00399a052openalex-snapshot
Synthesis of .alpha.,.beta.-unsaturated carbonyl compounds by palladium(II)-catalyzed dehydrosilylation of silyl enol ethers
inferredcites →https://doi.org/10.1021/jo00406a041openalex-snapshot
Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chloride
inferredcites →https://doi.org/10.1021/jo00798a025openalex-snapshot
Methylation of .alpha.-chloro ketones via halohydrin formation and rearrangement
inferredcites →https://doi.org/10.1021/jo00868a012openalex-snapshot
Dimethyl sulfoxide-trifluoroacetic anhydride. New reagent for oxidation of alcohols to carbonyls
inferredcites →https://doi.org/10.1021/jo01309a007openalex-snapshot
Stereochemistry of decarbalkoxylation of cyclic geminal diesters effected by water and lithium chloride in dimethyl sulfoxide
inferredcites →https://doi.org/10.1021/jo026302wopenalex-snapshot
A Practical Synthesis of the F-Ring of Halichondrin B via Ozonolytic Desymmetrization of a C2-Symmetric Dihydroxycyclohexene
inferredcites →https://doi.org/10.1021/jo051479mopenalex-snapshot
Halichondrin B: Synthesis of the C1−C22 Subunit
inferredcites →https://doi.org/10.1021/jo962231nopenalex-snapshot
Antitumor Polyether Macrolides: New and Hemisynthetic Halichondrins from the New Zealand Deep-Water Sponge Lissodendoryx sp.
inferredcites →https://doi.org/10.1021/jo971713bopenalex-snapshot
New Synthetic Route to the C.14−C.38 Segment of Halichondrins
inferredcites →https://doi.org/10.1021/jo981181eopenalex-snapshot
An Expeditious Synthesis of the C(38)−C(54) Halichondrin B Subunit
inferredcites →https://doi.org/10.1021/jo981342eopenalex-snapshot
Synthesis of a C(22)−C(34) Halichondrin B Precursor via Ring Opening−Double Ring Closing Metathesis
inferredcites →https://doi.org/10.1021/ol026504eopenalex-snapshot
A Novel Route to the F-Ring of Halichondrin B. Diastereoselection in Pd(0)-Mediated meso and C2 Diol Desymmetrization
inferredcites →https://doi.org/10.1021/ol0269805openalex-snapshot
Asymmetric Ni(II)/Cr(II)-Mediated Coupling Reaction: Stoichiometric Process
inferredcites →https://doi.org/10.1021/ol026981xopenalex-snapshot
Asymmetric Ni(II)/Cr(II)-Mediated Coupling Reaction: Catalytic Process
inferredcites →https://doi.org/10.1021/ol027389aopenalex-snapshot
Halichondrin B: Synthesis of a C1−C14 Model via Desymmetrization of (+)-Conduritol E
inferredcites →https://doi.org/10.1021/ol0473400openalex-snapshot
Synthetic Efforts toward the C22−C36 Subunit of Halichondrin B Utilizing Local and Imposed Symmetry
inferredcites →https://doi.org/10.1021/ol047661bopenalex-snapshot
New Catalytic Cycle for Couplings of Aldehydes with Organochromium Reagents
inferredcites →https://doi.org/10.1021/ol052084sopenalex-snapshot
A New Method for Translating the Asymmetric Ni/Cr-Mediated Coupling Reactions from Stoichiometric to Catalytic
inferredcites →https://doi.org/10.1021/ol052085kopenalex-snapshot
Surprisingly Efficient Catalytic Cr-Mediated Coupling Reactions
inferredcites →https://doi.org/10.1021/ol063113hopenalex-snapshot
Operationally Simple and Efficient Workup Procedure for TBAF-Mediated Desilylation: Application to Halichondrin Synthesis
inferredcites →https://doi.org/10.1021/ol702559eopenalex-snapshot
Highly Functionalized Pyranopyrans from Furans: A Synthesis of the C27−C38 and C44−C53 Subunits of Norhalichondrin B
inferredcites →https://doi.org/10.1021/ol702624nopenalex-snapshot
Increased Efficiency in Cross-Metathesis Reactions of Sterically Hindered Olefins
inferredcites →https://doi.org/10.1021/ol801093popenalex-snapshot
Further Improvement on Sulfonamide-Based Ligand for Catalytic Asymmetric 2-Haloallylation and Allylation
inferredcites →https://doi.org/10.1021/ol801421nopenalex-snapshot
Origin of Stereoselectivity in the Reduction of a Planar Oxacarbenium
inferredcites →https://doi.org/10.1021/ol990909qopenalex-snapshot
Synthesis and Activity of a New Generation of Ruthenium-Based Olefin Metathesis Catalysts Coordinated with 1,3-Dimesityl-4,5-dihydroimidazol-2-ylidene Ligands
inferredcites →https://doi.org/10.1039/c39920000810openalex-snapshot
Total synthesis of antitumour agent (+)-goniofufurone
inferredcites →https://doi.org/10.1039/c39950000383openalex-snapshot
Isolation and structure of halistatin 3 from the Western Pacific (Chuuk) marine sponge Phakellia sp
inferredcites →https://doi.org/10.1039/p19750001574openalex-snapshot
A new method for the deoxygenation of secondary alcohols
inferredcites →https://doi.org/10.1039/p19850002039openalex-snapshot
Asymmetric synthesis using chirally modified borohydrides. Part 3. Enantioselective reduction of ketones and oxime ethers with reagents prepared from borane and chiral amino alcohols
inferredcites →https://doi.org/10.1039/p19870000225openalex-snapshot
An approach to the construction of aromatic steroids using electrocyclic ring closure
inferredcites →https://doi.org/10.1039/p19920000887openalex-snapshot
Stereoselective syntheses of 2,4:5,6-di-O-isopropylidene-1 -C-phenyl- D -glycero- D -ido-hexitol and 2,4:5,6-di-O-isopropylidene-1 -C-phenyl- D -glycero- D -gulo-hexitol from D -glycero- D -gulo-heptono-γ-lactone. X-Ray structure of 1 -O-acetyl-2,4:5,6-di-O-isopropylidene-1-C-phenyl- D -glycero- D…
inferredcites →https://doi.org/10.1055/s-1991-28396openalex-snapshot
On the Stereochemical Divergence in the Conjugate Addition of Lithium Dimethylcuprate/Trimethylsilyl Chloride to γ-Alkoxy and γ-Ureido α,β-Unsaturated Esters
inferredcites →https://doi.org/10.1055/s-1994-22730openalex-snapshot
Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. 1. Stereoselective Synthesis of the C1-C13 FragmentviaConstruction of the B and A Rings by Kinetically and thermodynamically Controlled Intramolecular Michael Reactions.
inferredcites →https://doi.org/10.1055/s-1994-22731openalex-snapshot
Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. 2. Efficient Synthesis of C16-C26 FragmentsviaConstruction of the D Ring by a Highly Stereocontrolled Iodoetherification
inferredcites →https://doi.org/10.1055/s-1994-22732openalex-snapshot
Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. 3. Synthesis of C27-C36 SubunitviaCompletely StereoselectiveC-Glycosylation to the F Ring
inferredcites →https://doi.org/10.1055/s-1994-22733openalex-snapshot
Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. 4. Synthesis of the C37-C54 SubunitviaStereoselective Construction of Three Consecutive J, K, and L Rings
inferredcites →https://doi.org/10.1055/s-1997-697openalex-snapshot
The Synthesis of Aza[n]ladderanes and Azahomo[n]ladderanes Containing β-Lactams at the Terminus
inferredcites →https://doi.org/10.1124/mol.106.026641openalex-snapshot
Comparison of the Activities of the Truncated Halichondrin B Analog NSC 707389 (E7389) with Those of the Parent Compound and a Proposed Binding Site on Tubulin
inferredcites →https://doi.org/10.1159/000062488openalex-snapshot
The Halichondrins: Chemistry, Biology, Supply and Delivery
inferredcites →https://doi.org/10.1201/9781420039658openalex-snapshot
Anticancer Agents from Natural Products
inferredcites →https://doi.org/10.1246/bcsj.52.1989openalex-snapshot
A Rapid Esterification by Means of Mixed Anhydride and Its Application to Large-ring Lactonization
inferredcites →https://doi.org/10.1246/cl.1979.1389openalex-snapshot
TOP-TOP AND TOP-SKELETAL TORSION COUPLING EFFECTS ON THE MICROWAVE SPECTRA OF trans-ETHYLMETHYLETHER
inferredcites →https://doi.org/10.1246/cl.1980.1529openalex-snapshot
FLUORESCENCE DECAY OF 3,3′-DIETHYLTHIACARBOCYANINE IODIDE-SODIUM LAURYL SULFATE SYSTEM: DEAGGREGATION OF THE DYE AND DYE-DETERGENT AGGREGATE FORMATION ABOVE AND BELOW THE CRITICAL MICELLE CONCENTRATION
inferredcites →https://doi.org/10.1246/cl.1984.1389openalex-snapshot
COMBINATION OF BORANE-DIMETHYL SULFIDE COMPLEX WITH CATALYTIC SODIUM TETRAHYDROBORATE AS A SELECTIVE REDUCING AGENT FOR α-HYDROXY ESTERS. VERSATILE CHIRAL BUILDING BLOCK FROM (S)-(−)-MALIC ACID
inferredcites →https://doi.org/10.1246/cl.1984.1529openalex-snapshot
A FACILE SYNTHESIS OF α-C-RIBOFURANOSIDES FROM 1-O-ACETYL RIBOSE IN THE PRESENCE OF TRITYL PERCHLOLATE
inferredcites →https://doi.org/10.1248/cpb.28.3662openalex-snapshot
Hard acid and soft nucleophile system. IV. Removal of benzyl protecting group with boron trifluoride etherate and dimethyl sulflide.
inferredcites →https://doi.org/10.1248/cpb.42.683openalex-snapshot
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