About: Primary-Amine-Catalyzed Enantioselective Intramolecular Aldolizations

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scholarly article by Jian Zhou et al published 22 September 2008 in Angewandte Chemie International Edition

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 2008 (uk) im September 2008 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Jian Zhou et al published 22 September 2008 in Angewandte Chemie International Edition (en)
publication date	wds:Q58173088-3F9E236A-0ABB-43B3-9121-A5D59688936E
publication date	2008-09-22 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58173088-96E6EB0D-CD5F-46F1-AA3A-BE7FE112AA0B
language of work or name	English
cites work	wds:Q58173088-08DF1EBA-96E4-4E5B-9495-25F50649EE7D wds:Q58173088-0F91EEA9-E372-4965-923D-CA73B6E1BD17 wds:Q58173088-15962E12-133C-4B97-B6A1-2171FD27136D wds:Q58173088-22136D41-48BF-40DF-B4D7-683DFA6F3211 wds:Q58173088-25A722F8-AC5F-4C3F-A101-0A05EEFE6BAE wds:Q58173088-33CFFF33-D0D5-4317-8E08-D011C452F770 wds:Q58173088-3440896B-D01C-4576-ABEA-3598CFCB67E1 wds:Q58173088-3A999BAD-3D07-413E-A3BB-E1654323E926 wds:Q58173088-3D5CCE13-22F4-4158-AE25-2518F6EEF079 wds:Q58173088-40792664-498E-4643-B29D-7BFC8733B1CC wds:Q58173088-4B23434B-683F-41EE-A645-5B17D19BA183 wds:Q58173088-5460258B-6F5D-41F8-8AC0-55C9161B1172 wds:Q58173088-612913A2-A567-4B05-A6AA-9CA733D84E54 wds:Q58173088-8B7BDA76-800D-4380-9FEA-A4602C1EBCFF wds:Q58173088-8F25B320-F63E-466C-8B09-3FF82003852E wds:Q58173088-92BF74E4-929C-4079-9A42-9075D24D75A6 wds:Q58173088-9B621824-105F-4EAC-B52B-790566ED4320 wds:Q58173088-A08542ED-4204-485C-A01C-95BA11F90B76 wds:Q58173088-A3A84056-906A-4B43-B07E-0E0AC2E1FB88 wds:Q58173088-A61E2AC7-F2EE-4351-84A7-E28AF9AA6D7D wds:Q58173088-A896D88A-EBC6-4D6E-87F1-A78CAF621E68 wds:Q58173088-BFCC2C2B-61F7-46D1-808A-914AC29B9A56 wds:Q58173088-C27BAE1D-BB8F-4E31-886C-2051D1FFF68E wds:Q58173088-C35705C4-4702-4924-9FA5-6C9462BBD864 wds:Q58173088-C62A8E5B-3F00-4FF5-B2F7-FA4328975DF4 wds:Q58173088-CC77D8C8-5285-4E5C-8118-020B34424091 wds:Q58173088-CCAEC9F9-99DF-40EE-9261-13A1691F689A wds:Q58173088-D0851C51-2261-4BD5-87FC-0B18D71EB866 wds:Q58173088-D623D68B-F207-4859-A0E6-76A562758B8C wds:Q58173088-DC1BB564-9E0C-4C28-B611-CACC00E983EA wds:Q58173088-DED31CE6-8A37-4221-9BCF-7B777F15554A wds:Q58173088-E1F9D683-0677-44C0-A93C-A39AD9CD48C2 wds:Q58173088-E2101CAA-E530-47B0-B20D-368A74D51248 wds:Q58173088-EB713EE4-B106-458D-810A-A8FE81A41CCD wds:Q58173088-EDAC1914-2F97-47F2-B608-4497B8CF306D wds:Q58173088-F69E94BC-039F-4D09-AF68-A3A6D83C1F21
cites work	Substrate-directed stereoselectivity in vicinal diamine-catalyzed synthesis of warfarin Catalytic asymmetric epoxidation of cyclic enones Organocatalytic asymmetric Friedel-Crafts alkylation of indoles with simple alpha,beta-unsaturated ketones Highly asymmetric Michael addition to alpha,beta-unsaturated ketones catalyzed by 9-amino-9-deoxyepiquinine Readily accessible 9-epi-amino cinchona alkaloid derivatives promote efficient, highly enantioselective additions of aldehydes and ketones to nitroolefins Enantioselective Diels-Alder reaction of simple alpha,beta-unsaturated ketones with a cinchona alkaloid catalyst Enantioselective aldol cyclodehydrations catalyzed by antibody 38C2. Transition states of amine-catalyzed aldol reactions involving enamine intermediates: theoretical studies of mechanism, reactivity, and stereoselectivity Asymmetric synthesis of bicyclic intermediates of natural product chemistry New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures Neuartige asymmetrische Cyclisierung zu optisch aktiven Steroid-CD-Teilstücken Acute oral toxicity and bacterial translocation studies on potentially probiotic strains of lactic acid bacteria Asymmetric enamine catalysis Direct catalytic asymmetric synthesis of anti-1,2-amino alcohols and syn-1,2-diols through organocatalytic anti-Mannich and syn-aldol reactions Primary amino acids: privileged catalysts in enantioselective organocatalysis Organocatalytic Asymmetric Reaction Cascade to Substituted Cyclohexylamines New acetylenic compounds from the stony coral Montipora sp Small peptides as modular catalysts for the direct asymmetric aldol reaction: ancient peptides with aldolase enzyme activity Highly enantioselective organocatalysis of the Hajos-Parrish-Eder-Sauer-Wiechert reaction by the beta-amino acid cispentacin Highly enantioselective addition of ketones to nitroolefins catalyzed by new thiourea-amine bifunctional organocatalysts Highly enantioselective direct conjugate addition of ketones to nitroalkenes promoted by a chiral primary amine-thiourea catalyst Optically specific synthesis of estrone and 19-norsteroids from 2,6-lutidine Organocatalytic enantioselective synthesis of alpha-hydroxy phosphonates. Asymmetric direct aldol reaction of functionalized ketones catalyzed by amine organocatalysts based on bispidine Highly enantioselective direct aldol reaction catalyzed by cinchona derived primary amines. A simple primary-tertiary diamine-Brønsted acid catalyst for asymmetric direct aldol reactions of linear aliphatic ketones Design of acid-base catalysis for the asymmetric direct Aldol reaction A practical synthesis of (S)-2-cyclohexyl-2-phenylglycolic acid via organocatalytic asymmetric construction of a tetrasubstituted carbon center Design of highly enantioselective organocatalysts based on molecular recognition Highly enantioselective transfer hydrogenation of alpha,beta-unsaturated ketones Organocatalytic and highly enantioselective direct alpha-amination of aromatic ketones Design of an organocatalyst for the enantioselective Diels-Alder reaction with alpha-acyloxyacroleins Odor Incongruity and Chirality Scent through the looking glass Enantioselectivity of the musk odor sensation Synthetic studies of the HIV-1 protease inhibitive didemnaketals: stereocontrolled synthetic approach to the key mother spiroketals
author name string	wds:Q58173088-83EEC19A-5E8F-4ADC-8342-E5DC3A486C1C
author name string	Vijay Wakchaure
rdfs:label	Primary-Amine-Catalyzed Enantioselective Intramolecular Aldolizations (en) Primary-Amine-Catalyzed Enantioselective Intramolecular Aldolizations (nl)
skos:prefLabel	Primary-Amine-Catalyzed Enantioselective Intramolecular Aldolizations (en) Primary-Amine-Catalyzed Enantioselective Intramolecular Aldolizations (nl)
name	Primary-Amine-Catalyzed Enantioselective Intramolecular Aldolizations (en) Primary-Amine-Catalyzed Enantioselective Intramolecular Aldolizations (nl)
author	wds:Q58173088-3150CB9C-537B-467F-97F2-06787F8C8AC8 wds:Q58173088-A7EFC26A-1168-4EEA-908C-35DA98E395A1 wds:Q58173088-CA9AB796-53D3-4B18-8FFA-01C5AB21FC13
author	Philip Kraft Benjamin List Jian Zhou
title	wds:Q58173088-C7AA6D01-A532-48B9-9BB5-D6B40EF1EA8A
title	Primary-Amine-Catalyzed Enantioselective Intramolecular Aldolizations (en)
page(s)	wds:Q58173088-0C153409-C769-4102-8628-AF14BDC20D28
page(s)	7656-7658
instance of	wds:Q58173088-A6A40204-4606-4ABE-9FC8-6B43B651C981

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