Hybrid Single-Electron-Transfer-SN2 Reactions

DOI: 10.1021/ja00260a042

Source and publish data:

Journal of the American Chemical Society p. 8112 - 8113 (1987)

Update date:2022-08-05

Topics:

Authors:

Bordwell, F. G.

Harrelson, Jr., John A.

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

Article abstract of DOI:10.1021/ja00260a042

Full text of DOI:10.1021/ja00260a042

Products guided by the article

Product name:(9-Benzhydryl-9H-fluoren-9-yl)-diisopropyl-amine

Cas No:117959-64-5

R&D Labs maybe for 117959-64-5

Shanghai Standard Biotech Co., Ltd.

Contact:+86-18502101150

Address:Room 103, Building 2nd, NO.720, Cailun Road , Pudong District, Shanghai, China
chemonlinephramacistdepot

Contact:86-607-68073220

Address:1 ave na road jiahua st
Nanjing lanbai chemical Co.,Ltd.

Contact:+86-25-85499326

Address:Room 908, 9F Taiyue Building,No.285 Heyan Road
Kono Chem Co.,Ltd

website:http://www.konochem.com

Contact:86-29-86107037

Address:No.170 West Avenue,Xi’an 710082,China
Shanxi Tongji Pharmaceuticals Co., Ltd.

Contact:+86-359-3024784

Address:Xikuang South Road, Ruicheng County , Shanxi

Relevant to this article

Synthesis and evaluation of unsymmetrical bis(arylcarboxamides) designed as topoisomerase-Targeted anticancer drugs

Doi:10.1016/S0968-0896(01)00249-8
(2002)
Doi:10.1039/jr9520004019
(1952)
2,5 dicarbonyl sugars: new intermediates for synthesizing heterocyclic rings. II. Synthesis of N substituted 5 oxidopyridazinium derivatives from 2,5 diketo D gluconate

Doi:10.1248/cpb.22.1732
(1974)
The development of an aza-C-glycoside library based on a tandem staudinger/aza-wittig/ugi three-component reaction

Doi:10.1002/ejoc.201200923
(2012)
Stereoselective Synthesis of 1,1′-Disaccharides by Organoboron Catalysis

Doi:10.1002/anie.202004476
(2020)
Doi:10.1021/jm00330a023
(1965)

Article Doi