Controlling the reactivity of permanganate anion. Novel, stereospecific, dichlorination of olefins

DOI: 10.1016/S0040-4039(00)74342-5

Source and publish data:

Tetrahedron Letters p. 1831 - 1834 (1991)

Update date:2022-08-05

Topics:

Authors:

Marko Marko

Richardson

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

Article abstract of DOI:10.1016/S0040-4039(00)74342-5

Potassium permanganate reacts with oxalyl chloride to form a chlorine-containing manganese catalyst, of yet unknown structure, that stereospecifically trans-dichlorinates olefins.

Full text of DOI:10.1016/S0040-4039(00)74342-5

Products guided by the article

Product name:erythro 2,3-dichloroctane

Cas No:37464-71-4

R&D Labs maybe for 37464-71-4

HANGZHOU ICH BIOFARM CO.,LTD

Contact:+86-571-28186845

Address:Room 1224,Eastcom Mansion,398 Wensan Road,Hangzhou,310013 China
BioBioPha Co., Ltd

Contact:+86-871-65217109

Address:132 Lanhei Road, Kunming Institute of Botany, Chinese Academy of Sciences
Ceresking Ecology & Technology co.,ltd

Contact:86 22 66218397

Address:Room 1613, Zheshang Mansion, No. 1988, Yingbin Avenue, Binhai New District, Tianjin,China.
Chongqing KonAo Health Co.,Ltd

Contact:13687578375

Address:wuhan hubei china
Eastar Chemical Corporation

website:http://www.eastarchem.com/

Contact:1-800-898-2436

Address:1215 K Street, STE 1700

Relevant to this article

Doi:10.1021/jo01069a045
(1961)
Doi:10.1007/BF00475306
()
AMP deaminase inhibitors. 3. SAR of 3-(carboxyarylalkyl)coformycin aglycon analogues

Doi:10.1021/jm990448e
(2000)
Preparation of both enantiomers of 1-allyl-1,2,3,4-tetrahydro-β-carboline using allyltin reagents and a chiral auxiliary derived from L-proline

Doi:10.1016/S0040-4020(01)00684-6
(2001)
A new entry to asymmetric synthesis of 1-substituted 1,2,3,4-tetrahydro-β-carbolines employing a pyroglutamic acid derivative as a chiral auxiliary

Doi:10.1055/s-2002-31931
(2002)
Doi:10.1016/S0040-4039(01)94136-X
(1972)

Article Doi