About: Rigid and highly enantioselective catalyst for the dihydroxylation of olefins using osmium tetraoxide clarifies the origin of enantiospecificity

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About: Rigid and highly enantioselective catalyst for the dihydroxylation of olefins using osmium tetraoxide clarifies the origin of enantiospecificity Goto Sponge NotDistinct Permalink

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scholarly article by Elias James Corey & Mark C. Noe published December 1993 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1993 (uk) im Dezember 1993 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Elias James Corey & Mark C. Noe published December 1993 in Journal of the American Chemical Society (en)
publication date	wds:Q55892268-EEA5B532-FDFB-482E-87EB-33CAB67EA46B
publication date	1993-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q55892268-8D4CD204-158C-4A34-8230-E432CE8410F5
language of work or name	English
author name string	wds:Q55892268-87625249-20D6-4BF5-AFC2-9DC52D2F29BF
author name string	Mark C. Noe
rdfs:label	Rigid and highly enantioselective catalyst for the dihydroxylation of olefins using osmium tetraoxide clarifies the origin of enantiospecificity (en) Rigid and highly enantioselective catalyst for the dihydroxylation of olefins using osmium tetraoxide clarifies the origin of enantiospecificity (nl)
skos:prefLabel	Rigid and highly enantioselective catalyst for the dihydroxylation of olefins using osmium tetraoxide clarifies the origin of enantiospecificity (en) Rigid and highly enantioselective catalyst for the dihydroxylation of olefins using osmium tetraoxide clarifies the origin of enantiospecificity (nl)
name	Rigid and highly enantioselective catalyst for the dihydroxylation of olefins using osmium tetraoxide clarifies the origin of enantiospecificity (en) Rigid and highly enantioselective catalyst for the dihydroxylation of olefins using osmium tetraoxide clarifies the origin of enantiospecificity (nl)
author	wds:Q55892268-F3D6A244-6D85-420A-8AA8-3012A282C61F
author	Elias James Corey
title	wds:Q55892268-CE8BDC1E-F457-4EFA-A0BC-E27EA58E3739
title	Rigid and highly enantioselective catalyst for the dihydroxylation of olefins using osmium tetraoxide clarifies the origin of enantiospecificity (en)
page(s)	wds:Q55892268-E73B7F76-905F-4456-A26A-DD236EA3F937
page(s)	12579-12580
instance of	wds:Q55892268-08338B36-A7E3-43B0-85B0-CC2358F5496D
instance of	scholarly article
main subject	wds:Q55892268-76FBC168-473F-4F67-BFD1-2BABB3E07C12 wds:Q55892268-D476C8C3-D669-4F13-9BD0-B10975DC0602
main subject	osmium enantioselectivity
published in	wds:Q55892268-0100ED81-1C87-4F94-95B3-8439210AB8CB
published in	Journal of the American Chemical Society
issue	wds:Q55892268-E91058B3-7F61-49A3-92D6-0A39B433EDF9
volume	wds:Q55892268-A7A10CCA-8C38-4981-B0CC-A1884907C8A8
issue	26
volume	115
number of pages	wds:Q55892268-596C424E-458B-4C36-8F90-4BED1432D786
number of pages	2 (xsd:decimal)
DOI	wds:Q55892268-0997B0EE-F1E7-4101-A48B-08F1A9A8B09C
DOI	http://dx.doi.org/10.1021/JA00079A045
DOI	10.1021/JA00079A045
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55892268
is cites work of	Cinchona-alkaloid-catalyzed enantioselective direct aldol-type reaction of oxindoles with ethyl trifluoropyruvate. Dimeric Cinchona alkaloids Elucidation of the active conformation of cinchona alkaloid catalyst and chemical mechanism of alcoholysis of meso anhydrides X-ray crystallographic studies provide additional evidence that an enzyme-like binding pocket is crucial to the enantioselective dihydroxylation of olefins by OsO4—bis-cinchona alkaloid complexes Kinetic Investigations Provide Additional Evidence That an Enzyme-like Binding Pocket Is Crucial for High Enantioselectivity in the Bis-Cinchona Alkaloid Catalyzed Asymmetric Dihydroxylation of Olefins Electronic effects on the regio- and enantioselectivity of the asymmetric aminohydroxylation of O-substituted 4-hydroxy-2-butenoates. Experimental test of the [3+2]- and [2+2]-cycloaddition pathways for the bis-cinchona alkaloid-OsO4 catalyzed dihydroxylation of olefins by means of kinetic isotope effects Toward an Understanding of the High Enantioselectivity in the Osmium-Catalyzed Asymmetric Dihydroxylation. 4. Electronic Effects in Amine-Accelerated Osmylations Highly effective transition structure designed catalyst for the enantio- and position-selective dihydroxylation of polyisoprenoids Asymmetric Dihydroxylation of Alkenes Asymmetric direct α-alkylation of 2-oxindoles with Michler's hydrol catalyzed by bis-cinchona alkaloid-Brønsted acid via an SN1-type pathway. Updating the asymmetric osmium-catalyzed dihydroxylation (AD) mnemonic: Q2MM modeling and new kinetic measurements A QM/MM study of the asymmetric dihydroxylation of terminal aliphatic n-alkenes with OsO4.(DHQD)2PYDZ: enantioselectivity as a function of chain length Substrate Binding in the Asymmetric Dihydroxylation Reaction − Investigation of the Stereoselectivity in the Dihydroxylation ofCs-Symmetric Divinylcarbinol Derivatives A new chiral catalyst for the enantioselective Strecker synthesis of alpha-amino acids Silica gel supported bis-cinchona alkaloid: a highly efficient chiral ligand for heterogeneous asymmetric dihydroxylation of olefins A mechanistically guided design leads to the synthesis of an efficient and practical new reagent for the highly enantioselective, catalytic dihydroxylation of olefins Asymmetric dihydroxylation of trans-cinnamates under high-pressure conditions: substantial increase of turnover number
is cites work of	wds:Q35546281-42ED066D-D8B8-4A66-BD58-42A62A5D6407 wds:Q34375801-544EC06D-42AA-4151-9131-6714A6C462A7 wds:Q55968544-9269F33F-EF06-475F-B9F3-394BE91A8DAE wds:Q50237755-19B8804B-CBB2-4383-923D-2F2C48837F6D wds:Q61930887-7B0B78AF-75A5-476C-B084-ECF797F42100 wds:Q45198434-6D04A11C-403A-4EDB-8FF5-AAB9D6E30FD5 wds:Q46969550-156FD9F5-E396-4BB5-9165-DD9B73B4D000 wds:Q73194477-0EEB64D4-6163-4EA3-95AD-5727BAD428F0 wds:Q55968542-96F18358-66D3-4413-9B0A-309E08253E75 wds:Q55968534-6EFBE039-625E-4D59-B909-FC61F315C2A9 wds:Q34377511-B272ABEA-803E-48B2-BBE5-2AC656F9A9C0 wds:Q55968540-5B74459F-4725-43D4-A89D-07D084DF828A wds:Q55968541-3C11C202-73CA-41B1-A0BF-94ABFB28B6C6 wds:Q61945999-55F8FA2F-CEC0-40E1-8D96-892FBDA1F3AD wds:Q74561170-A4EA9E11-7F4D-4D4B-BF0A-5FABABD833CF wds:Q73926727-3700F65A-4A75-4B7F-BC77-4F0E3CB01672 wds:Q61946017-722199BB-DE97-43C0-AE6F-06B99092CB7F wds:Q42164356-86FF62B5-9974-4D4A-BCBA-2B41B2C5E45C

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