ALKANEPERSULFONIC ACIDS AS NEW OXIDIZING AGENTS IN THE BAYER-VILLIGER REACTION

DOI: 10.1007/BF00958296

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 1998 (1990)

Update date:2022-08-11

Topics:

Authors:

Safiullin, R. L.

Volgarev, A. N.

Komissarov, V. D.

Tolstikov, G. A.

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

Article abstract of DOI:10.1007/BF00958296

Full text of DOI:10.1007/BF00958296

Products guided by the article

Product name:Ethyl acetate

Cas No:141-78-6

R&D Labs maybe for 141-78-6

SNC | GOOD FORTUNE

Contact:0086-22-2822 1962 / 2822 1963

Address:B-808, No. 1, North-South Street, Hexi District,
Luzhou North Chemical Co., Ltd.

Contact:+86-830-2796784；+86-830-2796776

Address:Gaoba, Longmatan District, Luzhou, Sichuan Province
Shanghai better-in Medical Technology Co.,LTD.

Contact:+86-21-38921049

Address:Lane 720 zhangjianggaoke cailun road, Pudong, Shanghai, room 513
Kunshan Yalong Trading Co,.Ltd

Contact:86-512-57621185

Address:805-807 Room Hongqiao Mansion ,1088 West Qianjin Road, Kunshan, Jiangsu，China
Dongying J&M Chemical Co., Ltd,

Contact:546-8551108

Address:Room 1219, Zisheng Mansion, Zibo Road, Dongying, Shandong, China

Relevant to this article

Enzymatic Preparation of 2′-5′,3′-5′-Cyclic Dinucleotides, Their Binding Properties to Stimulator of Interferon Genes Adaptor Protein, and Structure/Activity Correlations

Doi:10.1021/acs.jmedchem.9b01062
(2019)
Doi:10.1139/v66-148
(1966)
Effect of cyclodextrin on the intramolecular catalysis of amide hydrolysis

Doi:10.1021/jo001011d
(2001)
A highly stable and versatile heterobifunctional fluoroalkylation reagent for preparation of fluorinated organic compounds

Doi:10.1039/c6ob00637j
(2016)
Sodium p-toluenesulfinate/copper(II) acetate in free radical reactions of 5-aryl substituted alkenes

Doi:10.1016/S0040-4020(99)00027-7
(1999)
Synthesis of an enantiopure 2-arylcyclohexanols from prochiral enol acetates by an enantioselective protonation/diastereoselective reduction sequence

Doi:10.1016/j.tetasy.2003.09.002
(2003)

Article Doi