About: Lewis base activation of Lewis acids. Catalytic enantioselective addition of silyl enol ethers of achiral methyl ketones to aldehydes

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About: Lewis base activation of Lewis acids. Catalytic enantioselective addition of silyl enol ethers of achiral methyl ketones to aldehydes Goto Sponge NotDistinct Permalink

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scientific article published on 01 June 2003

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) artículu científicu espublizáu en xunu de 2003 (ast) scientific article published on 01 June 2003 (en)
publication date	wds:Q73551712-6D031426-C562-4EAF-8947-58FB62FA2BE3
publication date	2003-06-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q73551712-623386F4-FD05-445B-B8DB-11EA96288361 wds:Q73551712-E707355C-170F-4681-A7DA-0E5237338B4A
author name string	Scott E Denmark John R Heemstra
rdfs:label	Lewis base activation of Lewis acids. Catalytic enantioselective addition of silyl enol ethers of achiral methyl ketones to aldehydes (en) Lewis base activation of Lewis acids. Catalytic enantioselective addition of silyl enol ethers of achiral methyl ketones to aldehydes (nl)
skos:prefLabel	Lewis base activation of Lewis acids. Catalytic enantioselective addition of silyl enol ethers of achiral methyl ketones to aldehydes (en) Lewis base activation of Lewis acids. Catalytic enantioselective addition of silyl enol ethers of achiral methyl ketones to aldehydes (nl)
name	Lewis base activation of Lewis acids. Catalytic enantioselective addition of silyl enol ethers of achiral methyl ketones to aldehydes (en) Lewis base activation of Lewis acids. Catalytic enantioselective addition of silyl enol ethers of achiral methyl ketones to aldehydes (nl)
title	wds:Q73551712-9A85ABB8-65A3-4280-B1E3-73CB24160E95
title	Lewis base activation of Lewis acids. Catalytic enantioselective addition of silyl enol ethers of achiral methyl ketones to aldehydes (en)
page(s)	wds:Q73551712-FACD3045-7027-4153-B18F-7032876A21EA
page(s)	2303-2306
instance of	wds:Q73551712-4FBC983C-B527-495A-AF47-54F74269483C
instance of	scholarly article
main subject	wds:Q73551712-671EEA77-85D2-49B7-B7C1-F3846308C6DA
main subject	enantioselectivity
PubMed ID	wds:Q73551712-1C80C389-888A-41B5-B69A-90A8B7E0DF06
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12816434
PubMed ID	12816434
published in	wds:Q73551712-B0084FD0-FF94-437D-A204-1F7CCEABEDE9
published in	Organic Letters
issue	wds:Q73551712-F518FEA6-168C-4E12-90E8-01B71B9619C7
volume	wds:Q73551712-143D71D8-2B2C-404A-934E-535C5D848A29
issue	13
volume	5
DOI	wds:Q73551712-B0772443-7F52-4B12-ABA1-4CA2732C716B
DOI	http://dx.doi.org/10.1021/OL034641L
DOI	10.1021/OL034641L
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73551712
is cites work of	N-silyl oxyketene imines are underused yet highly versatile reagents for catalytic asymmetric synthesis 5-(Pyrrolidine-2-yl)tetrazole: Rationale for the Increased Reactivity of the Tetrazole Analogue of Proline in Organocatalyzed Aldol Reactions Silyl ketene imines: highly versatile nucleophiles for catalytic, asymmetric synthesis
is cites work of	wds:Q42850708-D4D0A066-D4C4-43E3-AC03-43D17BDC2ED8 wds:Q42209687-0045BE63-DBEC-41F5-874A-F9C0A6868066 wds:Q64027838-B29A4A2A-7A24-47C1-8397-E1C02B162E6A

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