Asymmetric synthesis of rhopaloic acid a analogues and their biological properties

DOI: 10.3987/com-98-s(h)14

Source and publish data:

Heterocycles p. 35 - 38 (1999)

Update date:2022-08-03

Topics:

Authors:

Nishitani, Hiroko

Sasaoka, Asami

Tokumasu, Munetaka

Ohkata, Katsuo

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

Article abstract of DOI:10.3987/com-98-s(h)14

Some of rhopaloic acid A analogues were synthesized and their bioactivity was investigated on the basis of the inhibition of gastrulation of sea urchin embryos.

Full text of DOI:10.3987/com-98-s(h)14

Products guided by the article

Product name:(S)-3-((E)-(S)-2-Allyl-5,9-dimethyl-deca-4,8-dienoyl)-4-benzyl-oxazolidin-2-one

Cas No:220454-02-4

R&D Labs maybe for 220454-02-4

Sichuan WeiKeqi Biological Technology Co., Ltd.

Contact:86-028-81700200

Address:sichuan Chengdu Qingjiang Zhonglu 63号
Shanghai Cheerchem Co., Ltd.

Contact:86-21-50966856

Address:Building 5,300 Chuanzhan Road,Pudong New District,Shanghai
shandong zhongke taidou chemical co.,ltd

Contact:86-531-88682301

Address:Jinan shandong Province CHina
Suzhou Jingye Medicine & Chemical Co., Ltd

website:http://www.jingyechem.cn

Contact:+86-512-66658588

Address:No. 88, Sanlian Street, Jinfeng Road, Suzhou New District, Jiangsu Province, P. R. China
JiYi Chemical (Beijing) Co., Ltd.

Contact:+86-10-89385733

Address:Shilou Town of Fangshan District， Beijing

Relevant to this article

Rhenium(I) terpyridine π-bases: Reversible η²-coordination of ketones, aldehydes, and olefins in the terpyridine plane

Doi:10.1021/om980500p
(1999)
Ring closing metathesis as an efficient approach to branched cyclitols and aminocyclitols: A short synthesis of valiolamine

Doi:10.1016/S0040-4039(98)02539-8
(1999)
Doi:10.1021/ja01211a017
(1946)
1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 1: Discovery of the pyrrolidine scaffold and determination of its stereochemical requirements

Doi:10.1016/S0960-894X(01)00232-3
(2001)
Doi:10.1021/jo00823a028
(1971)
Synthesis of optically active 2-chloromethyl-2-oxazolines by the ortho- ester condensation method using triethyl orthochloroacetate

Doi:10.3987/COM-98-8407
(1999)

Article Doi