Studies on acetylenic compounds. 63. Synthesis of ibotenic acid.

DOI: 10.1248/cpb.15.1025

Source and publish data:

Chemical and pharmaceutical bulletin p. 1025 - 1031 (1967)

Update date:2022-08-04

Topics:

Authors:

Kishida Kishida

Hiraoka Hiraoka

Ide Ide

Terada Terada

Nakamura

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

Article abstract of DOI:10.1248/cpb.15.1025

Full text of DOI:10.1248/cpb.15.1025

NII-Electronic Library Service

Products guided by the article

Product name:2-benzyl-5-diethoxymethyl-isoxazol-3-one

Cas No:16446-45-0

R&D Labs maybe for 16446-45-0

Foreschem Co., Ltd

Contact:+86-533-3112891

Address:zibo
Changzhou Ansciep Chemical Co.,Ltd.

Contact:+86 519 8630 5871

Address:A-710 Boan International, 8 East Guangdian Road,Wujin,Changzhou
Wuxi D-Stone International Co., Ltd.

Contact:+86-510-82740567

Address:21F Hengtong Int'l Centre, 215Zhongshan Road, Wuxi, Jiangsu,China
Suzhou Ryan Pharmachem Technology Co.,Ltd

Contact:+86-0512-68780025

Address:B-301,No.2 Taishan Road,Suzhou New District,Jiangsu,P.R. China
Anhui New Star Pharmaceutical Development Co., Ltd

Contact:013956922763

Address:Floor 3, F9A, F Workshop, No.110 Kexue Road, High-Tech Development Zone, Hefei, Anhui ,China

Relevant to this article

Doi:10.1021/jo01270a056
(1968)
Preparation and reactions of N-(C-chloromercaptomethylene)-carbonic acid amides and their derivatives

Doi:10.1002/ardp.19673000707
(1967)
Doi:10.1002/zaac.19673520108
(1967)
Synthesis of highly functionalized, enantiomerically and diastereomerically pure cyclohexane derivates via Michael addition of chiral 3-tosyl-2-(2-oxoalkyl)-1,3-oxazolidines and methyl vinyl ketone

Doi:10.1055/s-1994-25687
(1994)
Novel, Potent, and Selective 5-HT₃ Receptor Antagonists Based on the Arylpiperazine Skeleton: Synthesis, Structure, Biological Activity, and Comparative Molecular Field Analysis Studies

Doi:10.1021/jm00014a021
(1995)
One-Pot Catalytic Enantioselective Synthesis of 2-Pyrazolines

Doi:10.1002/anie.201811471
(2019)

Article Doi