About: Asymmetric construction of quaternary carbon stereocenters: high stereoselection in Mukaiyama aldol reactions of 2-siloxyindoles with chiral aldehydes

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About: Asymmetric construction of quaternary carbon stereocenters: high stereoselection in Mukaiyama aldol reactions of 2-siloxyindoles with chiral aldehydes Goto Sponge NotDistinct Permalink

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scientific article published on 01 June 2005

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2005 (fr) наукова стаття, опублікована в червні 2005 (uk) artículu científicu espublizáu en xunu de 2005 (ast) scientific article published on 01 June 2005 (en)
publication date	wds:Q81855564-48870180-3574-445F-A492-866AEC1EE788
publication date	2005-06-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q81855564-0C6D0155-1742-4FB0-95F6-1888FF6D265F wds:Q81855564-26DF57F1-4133-46B6-AA69-778D5D89AC12 wds:Q81855564-37122039-0217-4FDF-8900-9D221B88E413 wds:Q81855564-58FC7C44-552B-490B-A495-8CC66BF99E9C
author name string	Susanta Adhikari Sebastien Caille Martin Hanbauer Vinh X Ngo
rdfs:label	Asymmetric construction of quaternary carbon stereocenters: high stereoselection in Mukaiyama aldol reactions of 2-siloxyindoles with chiral aldehydes (en) Asymmetric construction of quaternary carbon stereocenters: high stereoselection in Mukaiyama aldol reactions of 2-siloxyindoles with chiral aldehydes (nl)
skos:prefLabel	Asymmetric construction of quaternary carbon stereocenters: high stereoselection in Mukaiyama aldol reactions of 2-siloxyindoles with chiral aldehydes (en) Asymmetric construction of quaternary carbon stereocenters: high stereoselection in Mukaiyama aldol reactions of 2-siloxyindoles with chiral aldehydes (nl)
name	Asymmetric construction of quaternary carbon stereocenters: high stereoselection in Mukaiyama aldol reactions of 2-siloxyindoles with chiral aldehydes (en) Asymmetric construction of quaternary carbon stereocenters: high stereoselection in Mukaiyama aldol reactions of 2-siloxyindoles with chiral aldehydes (nl)
author	wds:Q81855564-7737494E-844E-46E7-B0EF-800004AE0FB5
author	Larry E. Overman
title	wds:Q81855564-5EAD9DBC-0996-4E2B-B6B6-706A6DF31717
title	Asymmetric construction of quaternary carbon stereocenters: high stereoselection in Mukaiyama aldol reactions of 2-siloxyindoles with chiral aldehydes (en)
page(s)	wds:Q81855564-1CA0B23D-5188-4651-9C2E-977C3A2878A6
page(s)	2795-2797
instance of	wds:Q81855564-FD226F88-CE83-4D47-BEDB-841B4C48DE6F
instance of	scholarly article
main subject	wds:Q81855564-BF9635E7-8F6C-4DB6-8501-10CC065E829F
main subject	chirality
PubMed ID	wds:Q81855564-5A21FB50-EA1C-4179-B43C-377F3DA8AB46
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/15957949
PubMed ID	15957949
published in	wds:Q81855564-EC9D0525-52E2-4318-8C9C-EAE230EE7D8A
published in	Organic Letters
issue	wds:Q81855564-FECB25E3-7C1D-4BD5-BFD0-D0FE780AB344
volume	wds:Q81855564-80882FB5-33AA-47B6-BBC7-B4F8272A31A9
issue	13
volume	7
DOI	wds:Q81855564-8EF18115-EE63-497F-A924-090D433742D7
DOI	http://dx.doi.org/10.1021/OL051172%2B
DOI	10.1021/OL051172+
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q81855564
is cites work of	Palladium-catalyzed enantioselective C-3 allylation of 3-substituted-1H-indoles using trialkylboranes Bis-arylidene oxindoles as anti-breast-cancer agents acting via the estrogen receptor A versatile synthesis of unsymmetrical 3,3'-bioxindoles: stereoselective Mukaiyama aldol reactions of 2-siloxyindoles with isatins. The palladium catalyzed asymmetric addition of oxindoles and allenes: an atom-economical versatile method for the construction of chiral indole alkaloids Enantioselective total synthesis of (+)-gliocladin C.
is cites work of	wds:Q30746277-C983D4C3-B5E6-4008-BC77-E63FBFE2995A wds:Q35621615-EA76C455-78B8-4177-A6D3-418E73F8F15A wds:Q36837325-BE991590-071E-4453-B900-8E7C827878CB wds:Q36853196-20082B5D-2461-4580-A057-56F0582A6D68 wds:Q37081491-342D10DF-5558-44DA-8792-4BAF9F2562EA

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