Thermal Generation and Dimerization of Metacyclophane

DOI: 10.1021/ja00259a050

Source and publish data:

Journal of the American Chemical Society p. 7887 - 7888 (1987)

Update date:2022-08-05

Topics:

Authors:

Kostermans, Gerardus B. M.

Dansik, Paul van

Wolf, Willem H. de

Bickelhaupt, Friedrich

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

Article abstract of DOI:10.1021/ja00259a050

Full text of DOI:10.1021/ja00259a050

Products guided by the article

Product name:anti-(4.4)metacyclophane

Cas No:111349-95-2

R&D Labs maybe for 111349-95-2

Anhui Gusheng Import&Export CO.,LTD

Contact:86-551-63662296

Address:Jinzhai Road NO.162 ,hefei, china
Shanghai Bojing Chemical Co., Ltd.

Contact:021-37122233

Address:6F Buildiing 11,No.388,Baifu Road,District Fengxian.Shanghai, China.
TIANJIN DONGRUXIANG MINERALS MARKETING CO.,LTD(expird)

Contact:22-58516360

Address:tianjin
Jiangxi Lanqi Fine Chemical S&T Co., Ltd.

Contact:+86-21-64891143

Address:XinJiShan Industrial Area, Zhangshu City, JiangXi Province, China
Anhui Biochem United Pharmaceutical Co., Ltd.

Contact:0086 551 5167062 / 5228268

Address:No. 30 Hongfeng Road, Hi-Tech Development Zone, Hefei (230088), China

Relevant to this article

Mitsunobu approach to the synthesis of optically active α,α-disubstituted amino acids

Doi:10.1021/ol802325h
(2009)
Discovery and synthesis of methyl 2,5-dimethyl-4-[2- (phenylmethyl)benzoyl]-1H-pyrrole-3-carboxylate (FPL 64176) and analogues: The first examples of a new class of calcium channel activator

Doi:10.1021/jm00071a004
(1993)
Doi:10.1021/ja01163a076
(1950)
Preparation of vinyl ethers using a Wittig approach, and their subsequent hydrogenation employing continuous-flow processing

Doi:10.1016/j.tetlet.2016.03.037
(2016)
A convenient synthesis of N-Boc-protected tert-butyl esters of phenylglycines from benzylamines

Doi:10.1016/S0040-4039(01)01651-3
(2001)
One-pot synthesis of 5-phenylimino, 5-thieno or 5-oxo-1,2,3-dithiazoles and evaluation of their antimicrobial and antitumor activity

Doi:10.1016/j.bmcl.2008.11.010
(2009)

Article Doi