Vinylcyclopropene Triplet Rearrangement Mechanisms: Mechanistic and Exploratoty Organic Photochemistry

DOI: 10.1021/ja00341a053

Source and publish data:

Journal of the American Chemical Society p. 622 - 624 (1983)

Update date:2022-08-05

Topics:

Authors:

Zimmerman, Howard E.

Fleming, Steven A.

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

Article abstract of DOI:10.1021/ja00341a053

Full text of DOI:10.1021/ja00341a053

Products guided by the article

Product name:1-phenyl-2-p-tolyl-3,5,5-trimethylcyclopentadiene

Cas No:84131-39-5

R&D Labs maybe for 84131-39-5

JinTan Pingsheng Chemical Co.,Ltd

Contact:+86-519-82828200

Address:NO.11Danfengxilu Road,Jintan City,Jiangsu,China
N&R INDUSTRIES,INC

Contact:Tel:+86-29-88764861 Fax:+86-29-88764861

Address:Rm#2107, Block A, Epin Meidao Building, Gaoxin Rd, Hi-Tech Zone, Xi’an, China
Nanjing Chemical Material Corp.(NCMC)

website:http://www.njchemm.com

Contact:0086-25-83172879

Address:B12 Technology and Innovation Building, Nanjing Tech University, No.5 New Model Road
HANGZHOU FOREWIN PHARMA CO., LTD

Contact:+86-571-89053961

Address:hangzhou
Chongqing Kangheyuecheng Pharmaceutical Technology Co., LTD

Contact:86+023-61183015-18725809730

Address:Degan Industrial Park Jiangjin Chongqing City

Relevant to this article

PYROPHOSPHATE TETRAESTER INTERMEDIATE OF COUPLING REACTIONS IN THE PHOSPHOTRIESTER APPROACH TO THE SYNTHESIS OF DEOXYOLIGORIBONUCLEOTIDES

Doi:10.1016/0040-4039(82)80153-6
(1982)
Parallel synthesis of tandem Ugi/Diels-Alder reaction products on a soluble polymer support directed toward split-pool realization of a small molecule library

Doi:10.1016/j.tetlet.2004.11.115
(2005)
Palladium-catalyzed reduction of alkynes employing HSiEt₃: stereoselective synthesis of trans- and cis-alkenes

Doi:10.1016/j.tet.2009.11.098
(2010)
Conjugates of Catecholamines. 1. N-Alkyl-Functionalized Carboxylic Acid Congeners and Amides Related to Isoproterenol

Doi:10.1021/jm00358a007
(1983)
Derivatives of β-adrenergic antagonists. N-nitrosopropranolol and N-hydroxypropranolol and its aldonitrone

Doi:10.1021/jm00357a027
(1983)
Doi:10.1246/bcsj.3.286
()

Article Doi