Synthesis of optically active α-trimethylsilyl Δ(α,β)-butenolides and their conversion into various butenolides and saturated γ-lactones

DOI: 10.1016/S0040-4039(00)97075-8

Source and publish data:

Tetrahedron Letters p. 6399 - 6402 (1990)

Update date:2022-08-06

Topics:

Authors:

Ito Ito

Okamoto Okamoto

Sato Sato

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

Article abstract of DOI:10.1016/S0040-4039(00)97075-8

Highly efficient method for synthesis of enantiomerically pure α,β-unsaturated butenolides having trimethylsilyl group at α-position (1) and their conversion into various butenolides and saturated γ-lactones are described.

Full text of DOI:10.1016/S0040-4039(00)97075-8

Products guided by the article

Product name:(R)-5-Cyclohexyl-3-trimethylsilanyl-5H-furan-2-one

Cas No:133216-90-7

R&D Labs maybe for 133216-90-7

Lianyungang Ningkang Chemical Co., Ltd

Contact:.+86-518-88588008

Address:http://www.chemnk.com
Shuanghe Bio-Technology Limited(expird)

Contact:+86-571-61710758,18968016640

Address:Jinqiao north road 916# Fuyang
Jinan Jinguilin Chemical Co.,Ltd

Contact:+86-531-81188412

Address:3rd floor of Torch Building, Huanyuan Rd, City of Jinan
SHANXI JINJIN CHEMICAL INDUSTRIAL CO.,LTD

website:http://www.jinjingroup.com

Contact:4009982989

Address:Economic And Technological Development Zone,Hejin?City,Shanxi Province?,China
Shanghai Norky Pharmaceutical Co., LTD.

website:http://www.norkypharm.com

Contact:86-21-61075300

Address:1165 Jiangning Road, Office 1502, Shanghai, China

Relevant to this article

N-Alkenyl Acylketene S,N-Acetals from 2,3-Dihydro-1,3-benzothiazoles and Carboxylic Anhydrides. X-Ray Molecular Structure of 2-(Butyrylmethylene)-N-(cyclohex-1-enyl)-2,3-dihydro-1,3-benzothiazole

Doi:10.1039/P19910001505
(1991)
GE-180: A novel fluorine-18 labelled PET tracer for imaging Translocator protein 18 kDa (TSPO)

Doi:10.1016/j.bmcl.2011.12.084
(2012)
Assembled structures and magnetic properties of viologen-[M(mnt) ₂] charge-transfer salts (mnt = maleonitriledithiolate; M = Cu, Ni, Pt)

Doi:10.1016/j.ica.2011.11.043
(2012)
Toward the development of a general chiral auxiliary. A remarkable, highly diastereoselective, auxiliary-mediated substitution: Application to an enantioselective synthesis of the cyclohexene subunit of (+)-tetronolide

Doi:10.1021/jo961585b
(1996)
A new prenylation method using the lithium enolate of prenal. Reaction with polyunsaturated aldehydes. A short access to retinal

Doi:10.1016/0040-4039(91)80022-X
(1991)
Synthesis, structures, and properties of two helical structures from rigid carboxylate ligand and flexible N-bridging ligands

Doi:10.1002/zaac.201100519
(2012)

Article Doi