About: Direct Catalytic Asymmetric Enolexo Aldolizations

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scholarly article by Chandrakala Pidathala et al published 23 June 2003 in Angewandte Chemie International Edition

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 2003 (uk) im Juni 2003 veröffentlichter wissenschaftlicher Artikel (de) article scientifique publié en 2003 (fr) scholarly article by Chandrakala Pidathala et al published 23 June 2003 in Angewandte Chemie International Edition (en)
publication date	wds:Q56288500-BBD75C7B-BB33-4193-B124-504BA05B9425
publication date	2003-06-23 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56288500-1A46D428-15D0-4CDB-827E-6A122BC5CEA2
language of work or name	English
author name string	wds:Q56288500-661B1F09-44D1-48A0-A8F3-86A45FD88A6C wds:Q56288500-9EBA1037-BF10-447E-8A15-E6FE687CAD76 wds:Q56288500-CE42C375-02CA-4020-BB5C-769C6EC1E1EC
author name string	Linh Hoang Chandrakala Pidathala Nicola Vignola
rdfs:label	Direct Catalytic Asymmetric Enolexo Aldolizations (en) Direct Catalytic Asymmetric Enolexo Aldolizations (nl)
skos:prefLabel	Direct Catalytic Asymmetric Enolexo Aldolizations (en) Direct Catalytic Asymmetric Enolexo Aldolizations (nl)
name	Direct Catalytic Asymmetric Enolexo Aldolizations (en) Direct Catalytic Asymmetric Enolexo Aldolizations (nl)
author	wds:Q56288500-1A20F987-020A-499C-9CDA-B169CBDBEEFC
author	Benjamin List
title	wds:Q56288500-E54A0CA6-9A2D-4A54-8CFA-7F28220E8579
title	Direct Catalytic Asymmetric Enolexo Aldolizations (en)
page(s)	wds:Q56288500-1057A8BE-178C-4FFB-8C87-9EA3B2730E06
page(s)	2785-2788
instance of	wds:Q56288500-A6CC9CE4-41E8-4FA0-9333-F1807D945B89
instance of	scholarly article
main subject	wds:Q56288500-1FF98BB8-5287-4E0A-B564-7246D2AFC9E3 wds:Q56288500-D2F80005-A50E-496C-B342-EEBD4E4EEAD5
main subject	general chemistry catalysis
PubMed ID	wds:Q56288500-3DEC6CF8-0761-4C82-A7EC-83F22AFBE3B7
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12820268
PubMed ID	12820268
published in	wds:Q56288500-E7940442-A9EE-48F9-8A42-CB236D41D4F9
published in	Angewandte Chemie International Edition
issue	wds:Q56288500-68F51A49-070C-4355-ABC7-F4630830DE78
volume	wds:Q56288500-D1905E2D-0258-487F-8787-81875B2CF4D2
issue	24
volume	42
DOI	wds:Q56288500-22A2C997-B20B-4EAD-B580-A130A2997411
DOI	http://dx.doi.org/10.1002/ANIE.200351266
DOI	10.1002/ANIE.200351266
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56288500
is cites work of	Asymmetric Catalysis Special Feature Part II: New mechanistic studies on the proline-catalyzed aldol reaction The ying and yang of asymmetric aminocatalysis Asymmetric enamine catalysis Molecular structure of proline. The direct catalytic asymmetric aldol reaction Enantioselective total synthesis and confirmation of the absolute and relative stereochemistry of streptorubin B. Asymmetric organocatalysis Current progress in the asymmetric aldol addition reaction Enantioselective direct aldol reactions catalyzed by L-prolinamide derivatives Direct amino acid catalyzed asymmetric synthesis of polyketide sugars Traceless chiral auxiliaries for the allene ether Nazarov cyclization The Diarylprolinol Silyl Ethers: Ten Years After. Synthesis of a new chiral pyrrolidine Biomimetic synthesis of Tramadol Organocatalytic Asymmetric Formal [3+2] Cycloaddition as a Versatile Platform to Access Methanobenzo[7]annulenes. Enantioselective, organocatalytic Morita-Baylis-Hillman and Aza-Morita-Baylis-Hillman reactions: stereochemical issues. Hydrophobically Directed Aldol Reactions: Polystyrene-SupportedL-Proline as a Recyclable Catalyst for Direct Asymmetric Aldol Reactions in the Presence of Water Development of a Modular Synthetic Route to (+)-Pleuromutilin, (+)-12-epi-Mutilins, and Related Structures. The cinchona primary amine-catalyzed asymmetric epoxidation and hydroperoxidation of α,β-unsaturated carbonyl compounds with hydrogen peroxide. Use of (S)-5-(2-Methylpyrrolidin-2-yl)-1H-tetrazole as a Novel and Enantioselective Organocatalyst for the Aldol Reaction Synthesis of Oxazolidinone and Tosyl Enamines by Tertiary Amine Catalysis Self-Assembly, Nematic Phase Formation, and Organocatalytic Behavior of a Proline-Functionalized Lipopeptide Mechanistic Study of Intramolecular Aldol Reactions of Dialdehydes Total Synthesis of 7,10-Epimer of the Proposed Structure of Amphidinolide N, Part I: Synthesis of the C1-C13 Subunit. Linear dialdehydes as promising substrates for aminocatalyzed transformations
is cites work of	wds:Q37029325-46FE4CFB-52F8-4CF3-8B5F-B564179348C2 wds:Q37023350-66336DE9-F005-44BE-BACB-5D8D38E1AC13 wds:Q48281137-A504CFA1-DE58-449A-BB3C-2022B071C668 wds:Q37649015-ACEF57CA-F1F0-4783-9E1D-ED90675E4F36 wds:Q29393358-82EA8BC8-1D26-431A-9F39-B914C2E8BA42 wds:Q35651445-8580B192-0284-492E-BEF4-EC56A219BBFA wds:Q37171476-5A394742-D0C7-4233-885C-B92E631EE892 wds:Q45205615-4E1E5857-3A59-442C-8A16-050795641CEB wds:Q37718530-78E68B02-D390-4C67-8E20-1AA67F55568E wds:Q59410819-2765C5C9-F1EB-41E8-9DC4-C6E35199AB73 wds:Q60246475-49EA3126-5F1F-4CB1-B183-89061F9CFF0C wds:Q34494706-6DA6FC4E-DF4E-4980-989D-C58A6C0BE9DD wds:Q43119454-CFD8A585-D948-47FE-AB2D-EE89208E50B3 wds:Q34687122-D8796C36-1CBC-46F8-B4E0-41C9A273248E wds:Q45066311-E6259C5C-8077-4169-8ADA-83359B8004FE wds:Q90061654-56CA4CCB-5CA4-405D-8048-46E022D34525 wds:Q41770311-235C351B-BD3A-4C73-80EB-14A4A6DA54D9 wds:Q57634148-D6B79CE8-8B1E-4621-8B38-107199A123EA wds:Q54443505-EED4795F-5A5D-4059-BE2C-DFEB8E355C6D wds:Q51535847-CF5B8881-6916-4725-9CCE-25FA83A5F668 wds:Q38285954-7D7FDC96-AEE9-4436-A118-529C193E979F wds:Q53792343-B5D76FF3-5759-4091-A3FD-64DBB14513BD wds:Q48162723-B3706295-43D6-4B90-AABF-AD65F8563525 wds:Q34397818-1D940EFC-2295-49C6-A4E2-6F2962E580ED wds:Q55113330-6E086C42-2A2A-4E97-9675-923303371295

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