INTRAMOLECULAR CYCLIZATION OF ACETYLENIC DERIVATIVES OF AROMATIC CARBOXYLIC ACID HYDRAZIDES

DOI: 10.1007/BF00954386

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 1534 (1983)

Update date:2022-08-02

Topics:

Authors:

Vasilevskii, S. F.

Shvatsberg, M. S.

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

Article abstract of DOI:10.1007/BF00954386

Full text of DOI:10.1007/BF00954386

Products guided by the article

Product name:7,8-dihydro-1-methyl-5-phenyl-4H-pyrazolo<3,4-d>-6,7-diazepin-8-one

Cas No:87612-15-5

R&D Labs maybe for 87612-15-5

Hangzhou Haichem Co.,Ltd.

Contact:+86-571-86025531 / 86024803

Address:1218-24 Guangyin Mansion,42 Fengqi East Road
JiYi Chemical (Beijing) Co., Ltd.

Contact:+86-10-89385733

Address:Shilou Town of Fangshan District， Beijing
Beijing Century Richap Chemistry Co.,Ltd

Contact:+86- 010-64455497

Address:Guannan County, Lianyungang City, Jiangsu Province, China
EnBridge PharmTech Co., Ltd.

website:http://www.enbridgepharm.com

Contact:+86-510-83591909

Address:Huishan Zone, Wuxi City, Jiangsu Province, P.R.China
Shanghai Yurui Biotechnology(Anyang) Pharmaceutical Co., Ltd

Contact:+86-0372-3662335 +86-0372-3661988

Address:hanling industrial park anyang

Relevant to this article

Ullmann C[sbnd]O coupling of sterically hindered secondary alcohols using excess amount of strongly coordinating monodentate ligands

Doi:10.1016/j.tetlet.2017.01.095
(2017)
REACTIONS OF VINYLIDENEDIPHOSPHONIC ACID WITH NUCLEOPHILES. COMMUNICATION 3. ADDITION OF THIOLS

Doi:10.1007/BF00962321
(1987)
Remote asymmetric trifluoromethylation induced by chiral sulfinyl group: Synthesis of enantiomerically pure 1-(2-naphthyl)-2,2,2-trifluoroethanol

Doi:10.1016/j.tetlet.2005.12.061
(2006)
Quinone-amine reactions, VIII: Synthesis of 6-aminobenzo[f]quinoxaline

Doi:10.1002/ardp.19833161016
(1983)
Total Synthesis of Racemic Silphinene

Doi:10.1021/jo00142a037
(1982)
Chirality Transfer in the Cholesterol Side Chain; Synthesis of (24R)- and (24S)-24-Hydroxycholesterols

Doi:10.1039/c39820000258
(1982)

Article Doi