About: Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates

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scholarly article by D. A. Evans et al published April 1981 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 1981 (uk) im April 1981 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by D. A. Evans et al published April 1981 in Journal of the American Chemical Society (en)
publication date	wds:Q56288437-11820DF3-81D1-4D4E-A21B-23DCC01E2F98
publication date	1981-04-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56288437-491A06DB-C987-4171-A020-65F1BF7E9406
language of work or name	English
author name string	wds:Q56288437-5B418728-4B18-4424-9C7B-CA5C871E7B68 wds:Q56288437-99710785-8068-4B87-9160-294FF80CBE5F wds:Q56288437-DE65187D-1BF8-451A-8B39-0CDD6125DF82
author name string	D. A. Evans J. Bartroli T. L. Shih
rdfs:label	Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates (en) Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates (nl)
skos:prefLabel	Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates (en) Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates (nl)
name	Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates (en) Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates (nl)
title	wds:Q56288437-A197867A-FF34-4169-82A4-10B162AB07DB
title	Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates (en)
page(s)	wds:Q56288437-A72147C1-C081-46E5-8D45-8CF54F9A462D
page(s)	2127-2129
instance of	wds:Q56288437-BB18FF73-5FD0-4F97-B292-70254A7605A6
instance of	scholarly article
main subject	wds:Q56288437-2C23896C-A458-4D6D-B3AD-E4F9EF58331E wds:Q56288437-468B6AEE-172B-4A99-A344-1EBF2C081DB7 wds:Q56288437-FE0B3266-A303-4518-977F-74281B178585
main subject	boron chirality enantioselectivity
published in	wds:Q56288437-DA5A1304-FE61-4D67-848D-2ADB650E6F6E
published in	Journal of the American Chemical Society
issue	wds:Q56288437-D2F2181C-8299-49BA-9F42-D6FBFC2698B2
volume	wds:Q56288437-C2AE0E5B-3828-4DD8-B564-2C3797F79F37
issue	8
volume	103
DOI	wds:Q56288437-287DBB93-31FC-4DF6-8030-9B816431594D
DOI	http://dx.doi.org/10.1021/JA00398A058
DOI	10.1021/JA00398A058
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56288437
is cites work of	Total synthesis, configuration, and biological evaluation of anguinomycin C. Total synthesis and determination of the absolute configuration of guadinomines B and C2. Steroid hormones controlling the life cycle of the nematode Caenorhabditis elegans: stereoselective synthesis and biology Total synthesis and study of 6-deoxyerythronolide B by late-stage C-H oxidation Stereoselective Organic Reactions: Catalysts for Carbonyl Addition Processes Precursor-directed biosynthesis: biochemical basis of the remarkable selectivity of the erythromycin polyketide synthase toward unsaturated triketides Generating Diverse Skeletons of Small Molecules Combinatorially Discovery of Mycobacterium tuberculosis protein tyrosine phosphatase A (MptpA) inhibitors based on natural products and a fragment-based approach The first direct and enantioselective cross-aldol reaction of aldehydes Forming all-carbon quaternary stereogenic centres in acyclic systems from alkynes Synthesis of alpha,beta-Unsaturated Amides by Olefin Cross-Metathesis The authors would like to thank the National Institutes of Health for generous support of this research, and D. Benitez, C. Bielawski, Dr. S. D. Goldberg, Dr. C. W. Lee, J. P. Mor Synthesis of chiral oxazolidin-2-ones by 1,2-amino alcohols, carbon dioxide and electrogenerated acetonitrile anion Synthesis of most polyene natural product motifs using just 12 building blocks and one coupling reaction (4R)-4-Benzyl-3-{(4S)-4-chloro-4-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]butano-yl}-1,3-oxazolidin-2-one Total synthesis and structure revision of didemnaketal B. "Black Swan events" in organic synthesis The Mukaiyama aldol reaction: 40 years of continuous development. Boron enolate chemistry toward the syntheses of polyketide stereotetrads Isolation and Structure Elucidation of Cruentarens A and B — Novel Members of the Benzolactone Class of ATPase Inhibitors from the MyxobacteriumByssovorax cruenta Nickel-Catalyzed Regiodivergent Approach to Macrolide Motifs Preparation, modification, and evaluation of cruentaren A and analogues Design and synthesis of dipeptidyl alpha',beta'-epoxy ketones, potent irreversible inhibitors of the cysteine protease cruzain Total synthesis of the anti-inflammatory and pro-resolving lipid mediator MaR1n-3 DPA utilizing an sp(3) -sp(3) Negishi cross-coupling reaction. Stereoselective synthesis of protectin D1: a potent anti-inflammatory and proresolving lipid mediator Syntheses of fumagillin and ovalicin Synthesis and conformational analysis of stevastelin C3 analogues and their activity against the dual-specific vaccina H1-related phosphatase Toxicity recognition of hepatotoxin, homologues of microcystin with artificial trapping devices. Synthesis and biological investigation of the β-thiolactone and β-lactam analogs of tetrahydrolipstatin Comparing the enantioselective power of steric and electrostatic effects in transition-metal-catalyzed asymmetric synthesis Modular total synthesis of rhizopodin: a highly potent G-actin dimerizing macrolide. Total syntheses and biological reassessment of lactimidomycin, isomigrastatin and congener glutarimide antibiotics Structure-based evolution of subtype-selective neurotensin receptor ligands The impact of the Mukaiyama aldol reaction in total synthesis β-Carbon activation of saturated carboxylic esters through N-heterocyclic carbene organocatalysis Asymmetric synthesis of naturally occurring spiroketals SuperQuat N-acyl-5,5-dimethyloxazolidin-2-ones for the asymmetric synthesis of alpha-alkyl and beta-alkyl aldehydes. Total synthesis and conformational studies of hapalosin, N-desmethylhapalosin and 8-deoxyhapalosin. Ester derived titanium enolate aldol reaction: chelation controlled diastereoselective synthesis of syn-aldols Synthesis of the protein phosphatase 2A inhibitor (4S,5S,6S,10S,11S,12S)-cytostatin. Syntheses of C17-C27 fragments of 20-deoxybryostatins for assembly using Julia and metathesis reactions. An efficient electrochemical method for N-acryloylation of oxazolidin-2-one chiral auxiliaries with α,α′-di- and trichloroketones Tetrahedral boronates as basic catalysts in the aldol reaction Aldol reactions mediated by a tetrahedral boronate Aldol reactions in polypropionate synthesis: High π-face selectivity of enol borinates from α-chiral methyl and ethyl ketones under substrate control Aldol reactions of methylketones using chiral boron reagents: A reversal in aldehyde enantioface selectivity An analysis of the diastereomeric transition state interactions for the kinetic deprotonation of acyclic carbonyl derivatives with lithium diisopropylamide Preparation and Application of Solid, Salt-Stabilized Zinc Amide Enolates with Enhanced Air and Moisture Stability. Synthesis and evaluation of hapalosin and analogs as MDR-reversing agents Asymmetric alkylations and aldol reactions: (1S,2R)-2-aminocyclopentan-1-ol derived new chiral auxiliary Synthesis, chromatographic resolution and chiroptical properties of carboxyibuprofen stereoisomers: major metabolites of ibuprofen in man Stereodefined acyclic trisubstituted metal enolates towards the asymmetric formation of quaternary carbon stereocentres Molecular recognition of diketide substrates by a beta-ketoacyl-acyl carrier protein synthase domain within a bimodular polyketide synthase Synthesis and Biological Evaluation of Lactimidomycin and Its Analogues. Total Synthesis and Complete Stereostructure of a Marine Macrolide Glycoside, (-)-Lyngbyaloside B. Total synthesis and biological evaluation of (-)-atrop-abyssomicin C. Synthesis of enantiomerically pure isotopomers of 2-phenylpropionic acids Total synthesis and structural elucidation of ent-micropyrone and (+)-ascosalipyrone

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