An Inverted Reactivity Series in the Reaction of tert-Butyl Radical with Nucleophyles

DOI: 10.1021/ja00291a079

Source and publish data:

Journal of the American Chemical Society p. 1450 - 1452 (1985)

Update date:2022-08-03

Topics:

Authors:

Russell, Glen A.

Khanna, R. K.

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

Article abstract of DOI:10.1021/ja00291a079

Full text of DOI:10.1021/ja00291a079

Products guided by the article

Product name:diethyl phenyl-tert-butylmalonate

Cas No:104330-19-0

R&D Labs maybe for 104330-19-0

FUJIAN SHANSHUI CHEMICAL CORP.LTD.

Contact:+86-151-59920036

Address:Jinqiao Gareden, jo@fj-xinyi.com
Wuhan Soleado Technology Co.,Ltd.

Contact:86-2783341481 18971291927

Address:RM2405 Unit 1 Builing 1, Taiyin Tower, Changqing Road,Wuhan China
Shenzhen JYMed Technology Co.,Ltd.

website:http://www.jymedtech.com

Contact:+86-755-26612112

Address:1#8,9/F, Biomedicine innovation Industrial Park, No.14, Jinhui Road, Pingshan Sistrict, Shenzhen, China
Sigma-Aldrich Chemie GmbH

website:http://www.sigmaaldrich.com

Contact:800 558-9160

Address:Industriestrasse 25CH-9471 Buchs SGSwitzerland
SHANXI JINJIN CHEMICAL INDUSTRIAL CO.,LTD

website:http://www.jinjingroup.com

Contact:86-574-13989382828

Address:Economic And Technological Development Zone,Hejin?City,Shanxi Province?,China

Relevant to this article

Selective Binding and Quantitation of Calcium with a Cobalt-Based Magnetic Resonance Probe

Doi:10.1021/jacs.9b02661
(2019)
Enantiospecific approach to a quinane skeleton related to pentalenolactones

Doi:10.1016/S0040-4039(97)10370-7
(1997)
Synthesis of Asialo GM₁. New insights in the application of sulfonamidoglycosylation in oligosaccharide assembly: Subtle proximity effects in the stereochemical governance of glycosidation

Doi:10.1021/ja9724957
(1998)
Syntheses and characterisation of amino(pentafluorophenyl)boranes. Crystal structure of [(Me₃Si)₂NB(C₆F₅)₂]

Doi:10.1016/S0277-5387(97)00239-8
(1998)
Doi:10.1016/S0040-4039(00)90044-3
(1965)
Phenolic cyclization. II. Syntheses of 6-hydroxy- and 8-hydroxy-1,2,3,4-tetrahydroisoquinoline derivatives (studies on the syntheses of heterocyclic compounds. CCXXXII.

Doi:10.1248/cpb.16.953
(1968)

Article Doi