CONVENIENT UNIMOLECULAR SOURCES OF ARYLOXYL RADICALS II-ARYLOXYOXALYL tert-BUTYLPEROXIDES

DOI: 10.1016/S0040-4039(01)80722-X

Source and publish data:

Tetrahedron Letters p. 4477 - 4480 (1989)

Update date:2022-08-03

Topics:

Authors:

Modarelli, David A.

Rossitto, Frank C.

Lahti, Paul M.

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

Article abstract of DOI:10.1016/S0040-4039(01)80722-X

UV photolysis and mild thermolysis of aryloxyoxalyl tert-butylperoxides provides a new unimolecular source of aryloxyl radicals, as shown by ESR and UV-vis spectroscopy.

Full text of DOI:10.1016/S0040-4039(01)80722-X

Products guided by the article

Product name:(2,4,6-tri-tert-butylphenoxy)oxalyl tert-butyl peroxide

Cas No:127213-23-4

R&D Labs maybe for 127213-23-4

Shanghai He Yang International Trading Co., Ltd.

Contact:+86-21-52043598

Address:Room 816, Blag.5, No.58 Huachi Road
Lian Xing Chemical Co.,Ltd.

Contact:0792-8228321

Address:10TH Floor No.121 binjiang Road Xunyang District
Joyochem Co., Ltd.

website:https://sdjingyuan.lookchem.com/

Contact:86-531-82687998

Address:Factory Building 11, Jinan Comprehensive free trade zone, Shandong, China
Sino-Japan Chemical Co., Ltd.

website:http://www.sjc.com.tw

Contact:(886) 2-2396-6223

Address:14Fl., No. 99. Sec. 2, Jen Ai Road
Chengdu CSH Pharmaceutical Co.,ltd

Contact:+86-(28)-85321971

Address:Block B,New Hope Int. Tian Fu New District, Chengdu, Sichuan, China

Relevant to this article

Copper-Catalyzed Three-Component Annulations of Alkenes, Nitrosoarenes, and N-Hydroxyallylamines To Form Fused Oxazinane/Isoxazolidine Heterocycles

Doi:10.1002/anie.201611388
(2017)
Selective and active transport of In³⁺ through N-nitrose-N-p-octadecylphenylhydroxylamine ammonium salt impregnated membrane

Doi:10.1246/bcsj.63.920
(1990)
Total synthesis of cyanolide A

Doi:10.1039/c0ob00971g
(2011)
Ammonium ylides for the diastereoselective synthesis of glycidic amides

Doi:10.1039/c0cc04821f
(2011)
Synthese und spektroskopische Charakterisierung ionischer Triphenyliodopnikogenhexafluoroarsenate des Typs <(C6H5)3EI>⁺^- (E=P, As, Sb, Bi); bakterizide Aktivitat von <(C6H5)3BiI>⁺^-

Doi:10.1016/0022-328X(89)85165-4
(1989)
Microwave assisted synthesis of bridgehead alkenes

Doi:10.1021/ol200244p
(2011)

Article Doi