Scholarly article on 1,1,1,4,4,4-hexadeuterio-2-(toluene-4-sulfonyloxy)-3-trideuteriomethyl-butane 42951-27-9 from Journal of the American Chemical Society p. 6370,6371,6372,6374,6375

DOI: 10.1021/ja00800a034

Source and publish data:

Journal of the American Chemical Society p. 6370,6371,6372,6374,6375 (1973)

Update date:2022-08-05

Topics:

Authors:

Lipnick Lipnick

Garbisch

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

Article abstract of DOI:10.1021/ja00800a034

Full text of DOI:10.1021/ja00800a034

Products guided by the article

Product name:1,1,1,4,4,4-hexadeuterio-2-(toluene-4-sulfonyloxy)-3-trideuteriomethyl-butane

Cas No:42951-27-9

R&D Labs maybe for 42951-27-9

Shandong Ailitong New Material Co.,Ltd

Contact:+86-536-3226266

Address:zhongjia village, putong town , qingzhou city,Shandong Province,China
Shanghai doly chemical Co.,Ltd

Contact:+86-21-34716221

Address:No.328,WuHe Roard,MinHang,ShangHai China
ShiJiaZhuang Dowell Chemical Co.,Ltd.

website:http://www.dowechem.com

Contact:+86-13463963265

Address:Xiyangling village, high tech Zone, Shijiazhuang，Hebei, China
Rely Chemicals Ltd.

Contact:+86-518-81061113

Address:No. 8 Lingzhou Road, Lianyungang, Jiangsu, China
Jiangsu Fengshan Group Co., Ltd.

Contact:86-25-86558671

Address:1903,Central International Mansion 105-6 North Zhongshan Road, Nanjing, China

Relevant to this article

Reactions of 1,1-Diarylethylenes and 1,1-Diarylimines with CF3OF

Doi:10.1021/jo01296a013
(1980)
Doi:10.1002/hlca.19740570624
(1974)
Oxidative nucleophilic substitution of hydrogen in nitroarenes with trifluoromethyl carbanions. Synthesis of trifluoromethyl phenols

Doi:10.1016/j.tet.2004.04.022
(2004)
Synthesis of novel mimetics of CMP-sialic acid as the inhibitors of sialyltransferases

Doi:10.1055/s-2002-33518
(2002)
Dialkylamino- and alkoxytrialkylstannanes as reagent for synthesis of organoboryl (trialkylsilyl) ketenes

Doi:10.1007/BF00717355
(1994)
Benzylidene acetal fragmentation route to 6-deoxy sugars: Direct reductive cleavage in the presence of ether protecting groups, permitting the efficient, highly stereocontrolled synthesis of β-D-rhamnosides from D-mannosyl glycosyl donors

Doi:10.1021/ja048070j
(2004)

Article Doi

DOI: 10.1021/ja00800a034