Scholarly article on 3,5-Cyclohexadiene-1,2-dicarboxylic acid, 3,6-diphenyl-, trans- 61716-47-0 from Journal of the American Chemical Society p. 2392,2394

DOI: 10.1021/ja01066a020

Source and publish data:

Journal of the American Chemical Society p. 2392,2394 (1964)

Update date:2022-08-03

Topics:

Authors:

Fieser Fieser

Haddadin

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

Article abstract of DOI:10.1021/ja01066a020

Full text of DOI:10.1021/ja01066a020

Products guided by the article

Product name:3,5-Cyclohexadiene-1,2-dicarboxylic acid, 3,6-diphenyl-, trans-

Cas No:61716-47-0

R&D Labs maybe for 61716-47-0

Jiangxi Biochem Co.,Ltd

Contact:86-791-86629460

Address:1-6F, 118 Xinzhou road, Nanchang, Jiangxi, China
Shanghai SMEC Trading Co., Ltd.

website:http://www.shanghaismec.com

Contact:+86-21-68811293

Address:ROOM 1101,NO.800 SHANGCHENG RD,SHANGHAI,CHINA
JINHUA HUAYI CHEMICAL CO., LTD.

website:http://www.chinahuayichem.com

Contact:86-579-82660891

Address:47-204 No.288, Shida St., Wuchem Dist., Jinhua,Zhejiang, 321004 China
HaiNan Periwinkle Pharmaceutical Co.,Ltd.

website:http://www.cchpharm.com/en/index.html

Contact:020-82208978

Address:Gongye road,Wuzhishan city,HaiNan province
Shanghai Sunway Pharmaceutical Technology Co.,Ltd.

Contact:+86-21-5161 3915

Address:Shanghai YangPu

Relevant to this article

Doi:10.1039/jr9470000160
(1947)
Reductive cleavage of N,N,N',N'-tetramethylphosphorodiamidate with lithium naphthalenide. A convenient procedure for deoxygenation of alcohols

Doi:10.1016/S0040-4039(97)10602-5
(1998)
Ring closing metathesis of sterically hindered 1,6 - dienes: A new approach to 5-membered branched cyclitols

Doi:10.1016/S0040-4039(99)01141-7
(1999)
SYNTHESIS OF ROOPEROL <1,5-BIS(3',4'-DIHYDROXYPHENYL)PENT-1-EN-4-YNE>

Doi:10.1016/0031-9422(88)80282-6
(1988)
A synthetic receptor for the Cbz-L-Ala-L-Ala-OH dipeptide sequence

Doi:10.1039/a903449h
(1999)
Novel analgesics and molecular rearrangements in the morphine--thebaine group. IX. A novel aromatisation during Hofmann degradation.

Doi:10.1039/j39690002225
(1969)

Article Doi

DOI: 10.1021/ja01066a020

Source and publish data: