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 Xingshun New Material Co., Ltd.

website:http://www.sd-xingshun.com

Contact:+86-519-86461196

Address:Middle of Luhua East Road, Dingtao District
A-Chem Technologies Co.,Ltd.

Contact:+86-512-69561895

Address:No.111, Building A4, 218 Xinghu Street, Suzhou Industrial Park, P. R. China
Richest Group Ltd.

Contact:+86 21 5017 5386

Address:No 999,Jiangyue Rd, Minhang Dist ,201114,Shanghai ,China
Xiamen Kaijia Imp & Exp Co., Ltd.

Contact:86-592-5101177

Address:Room406 Luhui Building No. 65 Haitian Road Huli Xiamen,China.
Shreeji pharma international

Contact:0091-265-2313036

Address:311, ATLANTIS HEIGHTS SARABHAI MAIN ROAD,VADIWADI ,VADODARA

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