About: Triflimide (HNTf2)-catalyzed aldehyde cross-aldol reaction using "super silyl" enol ethers

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About: Triflimide (HNTf2)-catalyzed aldehyde cross-aldol reaction using "super silyl" enol ethers Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 2006

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 2006 (uk) article scientifique (publié 2006) (fr) im Januar 2006 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 2006 (ast) artikull shkencor i botuar më 01 janar 2006 (sq) scientific article published on 01 January 2006 (en)
publication date	wds:Q80093289-E8653BB9-53CE-4CBE-8C44-50ADC96EE59E
publication date	2006-01-01 00:00:00Z (xsd:dateTime)
exact match	wds:Q80093289-E7E350AB-1CB4-469A-9546-CE5991291CD8
exact match	https://scigraph.springernature.com/pub.10.1038/nprot.2006.389
cites work	wds:Q80093289-29F68DB0-1605-40E8-8002-38B3E5301CA0 wds:Q80093289-43D0783D-0057-4CB6-849B-CB01E14457C3 wds:Q80093289-548E878B-6B94-428F-BE71-443B67C398D9 wds:Q80093289-646E8B7F-3624-4863-8BBF-C64D13573B38 wds:Q80093289-9BD8A2A4-6474-4F56-8762-548437CAEA09 wds:Q80093289-D6E50066-BC2C-4663-A956-ADC8A894E2D9
cites work	Tris(trimethylsilyl)silyl-governed aldehyde cross-aldol cascade reaction Crucial role of the ligand of silyl Lewis acid in the Mukaiyama aldol reaction Design of acid-base catalysis for the asymmetric direct Aldol reaction Strong counteranion effects on the catalytic activity of cationic silicon Lewis acids in Mukaiyama aldol and Diels-Alder reactions "Designer acids": combined acid catalysis for asymmetric synthesis. Protonated Chiral Catalysts: Versatile Tools for Asymmetric Synthesis
author name string	wds:Q80093289-77B399EB-083C-4F27-B156-628EBDC9A0C9 wds:Q80093289-E9F1A648-5254-49EA-8DD7-F9DC579200A8
author name string	Hisashi Yamamoto Matthew B Boxer
rdfs:label	Triflimide (HNTf2)-catalyzed aldehyde cross-aldol reaction using "super silyl" enol ethers (en) Triflimide (HNTf2)-catalyzed aldehyde cross-aldol reaction using "super silyl" enol ethers (nl) Triflimide (HNTf2)-catalyzed aldehyde cross-aldol reaction using "super silyl" enol ethers (sq)
skos:prefLabel	Triflimide (HNTf2)-catalyzed aldehyde cross-aldol reaction using "super silyl" enol ethers (en) Triflimide (HNTf2)-catalyzed aldehyde cross-aldol reaction using "super silyl" enol ethers (nl) Triflimide (HNTf2)-catalyzed aldehyde cross-aldol reaction using "super silyl" enol ethers (sq)
name	Triflimide (HNTf2)-catalyzed aldehyde cross-aldol reaction using "super silyl" enol ethers (en) Triflimide (HNTf2)-catalyzed aldehyde cross-aldol reaction using "super silyl" enol ethers (nl) Triflimide (HNTf2)-catalyzed aldehyde cross-aldol reaction using "super silyl" enol ethers (sq)
title	wds:Q80093289-3D9C062A-094E-47B8-A7FF-B49E45C792D8
title	Triflimide (HNTf2)-catalyzed aldehyde cross-aldol reaction using "super silyl" enol ethers (en)
page(s)	wds:Q80093289-4D7F87B0-189C-4577-8F9A-84329F2E6EF3
page(s)	2434-2438
instance of	wds:Q80093289-8A2883EF-F13B-4E8A-A7BB-457BCEE74353
instance of	scholarly article
PubMed ID	wds:Q80093289-E5DE5487-A198-4C9B-B4DD-1EC7F3D9B55F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17406488
PubMed ID	17406488
published in	wds:Q80093289-00253052-5534-4092-880B-0D908D036D4D
published in	Nature Protocols
issue	wds:Q80093289-11D23B3D-2A4B-4CF7-BDF6-EC208EF517F6
volume	wds:Q80093289-C04BBCB2-1C24-4D69-B2FD-E248AB0F671E
issue	5
volume	1
DOI	wds:Q80093289-C2D69CE0-0C99-4ED3-84E9-18BA6AB218A3
DOI	http://dx.doi.org/10.1038/NPROT.2006.389
DOI	10.1038/NPROT.2006.389
Dimensions Publication ID	wds:Q80093289-7F8D3FF1-FE0D-4DD7-838C-609CA36F19ED
Dimensions Publication ID	1020961267
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q80093289
is cites work of	Rapid, one-pot synthesis of β-siloxy-α-haloaldehydes. β-Siloxy-α-haloketones through highly diastereoselective single and double mukaiyama aldol reactions A triple-aldol cascade reaction for the rapid assembly of polyketides Generation of organolithium compounds bearing super silyl ester and their application to Matteson rearrangement Synthesis of β-hydroxy-α-haloesters through super silyl ester directed syn-selective aldol reaction.
is cites work of	wds:Q42168645-469422EA-B49E-40A8-A981-E1585346BFEC wds:Q42907161-51F25C9C-00B1-431F-A25A-953AED883B20 wds:Q38572989-F3396F82-8492-47E3-9AD7-F46D1CB23BDF wds:Q42418182-8AD24261-2204-4CAB-B2AC-8676AE9CCACF wds:Q42061041-164E1F98-4CAE-40F3-9046-37FBD6D6F055

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