Novel analgesics and molecular rearrangements in the morphine--thebaine group. IX. A novel aromatisation during Hofmann degradation.

DOI: 10.1039/j39690002225

Source and publish data:

Journal of the Chemical Society. Perkin transactions I p. 2225 - 2228 (1969)

Update date:2022-08-03

Topics:

Authors:

Bentley Bentley

Crocker Crocker

Walser Walser

Fulmor Fulmor

Morton Morton

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

Article abstract of DOI:10.1039/j39690002225

Full text of DOI:10.1039/j39690002225

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:(+/-)-7-(4-Hydroxy-2-isopropyl-phenyl)-1,2-dimethoxy-8-vinyl-naphthalin

Cas No:24482-06-2

R&D Labs maybe for 24482-06-2

SAGECHEM LIMITED

website:http://www.sagechem.com

Contact:+86-571-86818502

Address:Room C1301, New Youth Plaza, 8 Jia Shan Road, Hangzhou, China
HANGZHOU PANYU CHEMICAL CO.,LIMITED

Contact:+86-571-86578491

Address:Rm 605, NO.1870 Binsheng Road,Binjiang Dist, Hangzhou, China
NINGBO YINLIANG FOREIGN TRADE CO., LTD.

Contact:+86-574-87834016 / 87898057

Address:23F NO.666JINYU ROAD,YINGZHOU DISTRICT,NINGBO.CHINA
ABA Chemicals (Shanghai) Limited

Contact:021- 5115 9199-232

Address:Suite 18D, #201 Ningxia Road,
Daqing New Century Fine Chemical Co., Ltd.(expird)

Contact:010-57126694

Address:No.39, jinxing cun, honggang district

Relevant to this article

Tricyclic isoxazoles are novel inhibitors of the multidrug resistance protein (MRP1)

Doi:10.1016/S0960-894X(02)00051-3
(2002)
Doi:10.1021/ja01052a051
(1969)
A Simple Method for the Reduction of the 7,8-Double Bond of Steroidal 5,7-Dienes

Doi:10.1039/c39820001169
(1982)
HRh4 as a hydrogenation and isomerization catalyst

Doi:10.1016/0022-328X(95)05454-W
(1995)
Structural, odd-even chain alternation and thermal investigation of a homologous series of anhydrous silver(i) n-alkanoates

Doi:10.1039/c2dt11638c
(2012)
Synthesis of biologically important guanidine-containing molecules using triflyl-diurethane protected guanidines

Doi:10.1055/s-1999-3653
(1999)

Article Doi