Scholarly article on 4,4-Dicyclopropylcyclohex-2-en-1-on 34189-10-1 from Journal of the American Chemical Society p. 4232 - 4236

DOI: 10.1021/ja00746a024

Source and publish data:

Journal of the American Chemical Society p. 4232 - 4236 (1971)

Update date:2022-08-05

Topics:

Authors:

Hahn,R.C.

Jones,G.W.

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

Article abstract of DOI:10.1021/ja00746a024

Full text of DOI:10.1021/ja00746a024

Products guided by the article

Product name:4,4-Dicyclopropylcyclohex-2-en-1-on

Cas No:34189-10-1

R&D Labs maybe for 34189-10-1

Chongqing maohuan Chemicals Co., Ltd

website:http://www.bschem.com

Contact:+86 13996103726

Address:Chongqing Nan'an District Tu Town
Koning Pharmchem Co., Ltd.

website:http://www.koningpharm.com

Contact:86-574-87369228

Address:Lingqiao Road
Allright GC (Jinan) Biotechnology Ltd.

website:https://www.argcbiotech.com/

Contact:86-18405413579-

Address: No.27566 of Jingshiroad, Huaiyin District, Jinan City(250011), Shandong Province, China.
HOME-PHARMACY

Contact:+380934623255

Address:Gagarina avenue
jiangsu haian chemical co.,ltd.

Contact:86-513-15851283853

Address:No.99,Changjiang West Road,Haian County,Jiangsu Province,China

Relevant to this article

Phosphoramidate protides of five flavones and their antiproliferative activity against HepG2 and L-O2 cell lines

Doi:10.1016/j.ejmech.2016.02.012
(2016)
Recyclable iron/graphite catalyst for c-s cross coupling of thiols with aryl halides under ligand-free conditions

Doi:10.1055/s-0029-1219801
(2010)
Environment friendly chemoselective deprotection of acetonides and cleavage of acetals and ketals in aqueous medium without using any catalyst or organic solvent

Doi:10.1007/s12039-013-0514-7
(2013)
A flexible strategy for the synthesis of tri- and tetracyclic lupin alkaloids: Synthesis of (+)-cytisine, (±)-anagyrine, and (±)-thermopsine

Doi:10.1002/anie.200504015
(2006)
Synthesis of a new series of biologically interesting 6′-chloro- 1′,1′-dioxospiro[4H-benzo[d][1,3,7]oxadiazocine-4, 3′(2′H)-[1,4,2]benzodithiazine]-2,6(1H,5H)dione derivatives

Doi:10.1007/s00706-013-1010-y
(2013)
Use of fluoroform as a source of difluorocarbene in the synthesis of difluoromethoxy- and difluorothiomethoxyarenes

Doi:10.1021/jo401392f
(2013)

Article Doi

DOI: 10.1021/ja00746a024