Formation of Fused Tricyclic Azetidinones and Pyrrolidinones by Intramolecular SH2 Processes

DOI: 10.1021/jo00253a028

Source and publish data:

Journal of Organic Chemistry p. 4339 - 4348 (1988)

Update date:2022-09-26

Topics: Intramolecular Fused Formation Tricyclic Pyrrolidinones

Authors:

Beckwith, A. L. J.

Boate, D. R.

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

Article abstract of DOI:10.1021/jo00253a028

Treatment of a variety of suitably substituted sulfides of N-(o-halobenzyl)- or N-(o-halophenyl)azetidinone (e.g., 4 and 8) and -pyrrolidinone (e.g., 12 and 14) systems with either tributylstannane or tributyltin deuteride affords, by aryl radical substit

Full text of DOI:10.1021/jo00253a028

Products guided by the article

Product name:2-Pyrrolidinone, 1-[(2-bromophenyl)methyl]-5-(methylthio)-

Cas No:115363-88-7

R&D Labs maybe for 115363-88-7

Kaymossy BioChem Tech Co., Ltd

website:http://www.kaimosi.com

Contact:0571-87191913/0571-87199097

Address:Room 215, Building 3rd, No.288 Ningxia Road, Qingdao city, China
Hubei Danao Pharmaceutical Co.,Ltd.

website:http://www.danaopharm.com

Contact:+86-719-5251167

Address:Fandan Road,Danjiangkou,Hubei
Chengdu Pukang Biotechnology Co., Ltd

website:http://www.pu-kang.com

Contact:86-028-63976226

Address:No. 868 Xiwang Road,Xinjin county,Chengdu city, China
shijiazhuang baisheng chem co.; ltd

Contact:86-0311-80790826

Address:shijiazhuang hebei
Beijing Tianjia Chemical Science & Technology Co.,Ltd

Contact:86-0550-2392698

Address:No.388, Shiliang Road (East),

Relevant to this article

A novel synthesis and transformations of isothiochroman 2,2-dioxide

Doi:10.1016/j.tetlet.2012.05.163
(2012)
Synthesis of (-)-Flavoskyrins by Catalyst-Free Oxidation of (R)-Configured Dihydroanthracenones in Aqueous Media and Its (Bio)synthetic Implications

Doi:10.1021/acs.orglett.0c03121
(2020)
First example of C-3 alkylation of indoles with activated azetidines catalyzed by indium(III) bromide

Doi:10.1055/s-0028-1087957
(2009)
Role of the A^1,3 Allylic Interaction on the Stereochemistry of Formation of Schiff's Bases derived from Bicyclo<2.2.1>hept-5-en-2-one and 7-Oxabicyclo<2.2.1>hept-5-en-2-one

Doi:10.1039/P29880000865
(1988)
A new route to 2,2′,3,3′-tetrasubstituted binaphthyls

Doi:10.1016/j.tetlet.2009.03.008
(2009)
Synthese und Bestimmung des Chiralitaetssinns von (+)-(R)-1-Azabicyclo<3.3.1>nonan-2-on

Doi:10.1002/hlca.19870700802
(1987)

Article Doi