Chiral tin(II) Lewis acid-mediated enantioselective aldol reactions: Synthesis of both enantiomers using similar types of chiral sources

DOI: 10.1016/0957-4166(95)00335-M

Source and publish data:

Tetrahedron Asymmetry p. 2565 - 2569 (1995)

Update date:2022-07-31

Topics:

Authors:

Kobayashi

Horibe Horibe

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

Article abstract of DOI:10.1016/0957-4166(95)00335-M

Chiral tin(II)-Lewis acid-mediated aldol reactions of various enolates with an aldehyde were investigated by using chiral diamine 2. Based on these reactions, both enantiomers of aldol adducts were prepared using similar types of chiral sources.

Full text of DOI:10.1016/0957-4166(95)00335-M

Products guided by the article

Product name:(2S,3R)-2-tert-Butylsulfanyl-3-hydroxy-3-phenyl-thiopropionic acid S-ethyl ester

Cas No:171627-18-2

R&D Labs maybe for 171627-18-2

YingYing Pharmaceutical Co.,Ltd

Contact:86-18854126208

Address:55#, yingxiongshan road
Shanxi Sanwei Group Co.,Ltd

Contact:0086-357-6662688

Address:Zhaocheng town, Hongtong County, Linfen City, Shanxi Province
Chengdu ZY Biochemical Technology Co., LTD

Contact:0086-28-88680086

Address:170 Qingpu Road, Shouan Town, Pujiang County
Tosta Enterprise Co., Ltd.

Contact:+86-134-5286-9121

Address:Add: Wing Tuck Commercial Centre, 177-183 Wing Lok Street, Hong Kong,
wuxi leji biology technology co., LTD

website:http://www.lejibio.com/

Contact:18362718864

Address:The Nanyue Road No. 2, Yixing City, Jiangsu Province

Relevant to this article

Five new pregnane glycosides from the stems of Marsdenia tenacissima

Doi:10.1080/10286020.2011.570263
(2011)
Fischer indolization of ethyl pyruvate 2-bis(2-methoxyphenyl)hydrazone and new insight into the mechanism of Fischer indolization. (Fischer indolization and its related compounds. XXVII)

Doi:10.1248/cpb.43.1287
(1995)
Preparation of Small Ring Carbocycles via Intramolecular Oxidative Coupling of Bisenolates Derived from α,ω-Diesters

Doi:10.1021/jo00391a060
(1987)
Synthesis of a 3-Deoxy-D-arabino-2-heptulosonic Acid Derivative

Doi:10.1021/jo00127a047
(1995)
Michael addition of ethyl anthranilate and phenyl monothioanthranilate to acetylenic esters: experimental and theoretical results

Doi:10.1007/s11224-021-01735-9
(2021)
Use of the dithiasuccinoyl (Dts) amino protecting group for solid-phase synthesis of protected peptide nucleic acid (PNA) oligomers

Doi:10.1021/jo9824394
(1999)

Article Doi