VINYL RADICAL GENERATION WITH SELENOBORANE AND ITS APPLICATION TO CYCLIZATION REACTION OF ENYNES

DOI: 10.1016/S0040-4039(00)97996-6

Source and publish data:

Tetrahedron Letters p. 5927 - 5930 (1990)

Update date:2022-08-02

Topics:

Authors:

Kataoka, Tadashi

Yoshimatsu, Mitsuhiro

Shimizu, Hiroshi

Hori, Mikio

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

Article abstract of DOI:10.1016/S0040-4039(00)97996-6

Tris(methylseleno)- and tris(phenylseleno)boranes added to acetylenes to afford methylseleno- and phenylseleno-substituted Z-vinylselenides in high yields.The addition reactions proceeded by way of free radicals and were applied to cyclization reactions o

Full text of DOI:10.1016/S0040-4039(00)97996-6

Products guided by the article

Product name:(E/Z)-1-Phenylselenododec-1-ene

Cas No:132330-38-2

R&D Labs maybe for 132330-38-2

AURORA CHEMICAL CO., LTD

Contact:86-532-68629711 13780605697

Address:NO 220 YANAN 3 ROAD,(POST ADMINISTRATION BUILDING),QINGDAO,CHINA
xujianqiang

Contact:86-21-57725962

Address:shanghai
Shanghai Micro-mega Industry Co., Ltd.

Contact:0086-21-34628682;57153848

Address:Rm413,No.413,West Meilong Road, Minhang District,Shanghai P R China
Shanghai Mio Chemical Co., Ltd

Contact:0086 21- 64401188-622

Address:16 Floor NO.2 Jiefang Building, No. 4855 Dushi Road, 201100 Shanghai, P.R.China
Nanjing Habo Medical Technology Co., Ltd.

Contact:025－85769882

Address:No.108. Ganjiabian east. Qixia District .Nanjing

Relevant to this article

Experimental and Theoretical Study of Orientation in the Nitration of Dithieno<3,4-b:3',4'-d>pyridine

Doi:10.1021/jo00004a046
(1991)
A general route to 4-C-substituted pyrimidine nucleosides

Doi:10.1055/s-2007-965935
(2007)
An efficient bismuth(III) chloride-catalyzed synthesis of 1,1-di-arylalkenes via Friedel-Crafts reaction of acyl chloride or vinyl chloride with arenes

Doi:10.1002/adsc.200606157
(2006)
Indonesian medicinal plants. XXIV. Stereochemical structure of perseitol x K+ complex isolated from the leaves of Scurrula fusca (Loranthaceae).

Doi:10.1248/cpb.50.489
(2002)
Expanding the Boundaries of Water-Tolerant Frustrated Lewis Pair Hydrogenation: Enhanced Back Strain in the Lewis Acid Enables the Reductive Amination of Carbonyls

Doi:10.1002/anie.201703591
(2017)
An algorithm for the deconvolution of mass spectrosopic patterns in isotope labeling studies. Evaluation for the hydrogen-deuterium exchange reaction in ketones

Doi:10.1021/jo070831o
(2007)

Article Doi