Thio-Claisen rearrangements. An asymmetric synthesis of 4,4-disubstituted cyclohexenones with vicinal quaternary and tertiary stereocenters

DOI: 10.1021/ja00085a059

Source and publish data:

Journal of the American Chemical Society p. 2633 - 2634 (1994)

Update date:2022-07-29

Topics:

Authors:

Devine, Paul N.

Meyers Meyers

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/ja00085a059

Full text of DOI:10.1021/ja00085a059

Products guided by the article

Product name:(S)-2-Methyl-2-((R)-1-methyl-allyl)-5-oxo-hexanal

Cas No:155395-83-8

R&D Labs maybe for 155395-83-8

Weifang Adde Economic And Trade Co.,LTD.

Contact:86-536-8885548

Address:Room 1402,Wanda Plaza B Block,No.958,Yuanfei Road,Kuiwen District
jiangsu hualin chemical co.,ltd.

Contact:86-25-87787402

Address:jaingsu,china
Dongguan Albiya Energy Science and Technology Co.,Ltd

Contact:+86-769-22181286

Address:Huanan Industial Park, Dongguan,China
Wuhan Better Organic Technology Inc.

Contact:13307163183

Address:Wuhan Economic&Technology Development Zone, Hubei
Shanghai TBBMed Co.,Ltd

website:http://www.tbbmed.com

Contact:86--21-50498136

Address:Room 6002, Building 7-1, No.160 Basheng Road,Pudong Area,Shanghai China

Relevant to this article

Versatile ruthenium(ii)-catalyzed C-H cyanations of benzamides

Doi:10.1039/c3cc49502g
(2014)
"sulfolefin": A mixed sulfinamido-olefin ligand in enantioselective rhodium-catalyzed addition of arylboronic acids to trifluoromethyl ketones

Doi:10.1039/c3ob41888j
(2014)
Syntheses of hydroxamic acid-containing bicyclic β-lactams via palladium-catalyzed oxidative amidation of alkenes

Doi:10.1021/jo402544p
(2014)
Synthesis of macrolactam analogues of radicicol and their binding to heat shock protein Hsp90

Doi:10.1039/c3ob42211a
(2014)
Generation of N-Acyl Iminium Ions from Ionization-Rearrangement Reactions of N-Triflyloxy Amides

Doi:10.1016/S0040-4039(00)76872-9
(1994)
Facile removal of 4-phenyl-oxazolidinethione auxiliary with EtSH mediated by DBU

Doi:10.1016/j.tetlet.2004.08.113
(2004)

Article Doi