Scholarly article on 1.2-Bis(tosyloxydideuteromethyl)cyclobutan 35630-09-2 from Journal of the American Chemical Society p. 1675,1680

DOI: 10.1021/ja00760a041

Source and publish data:

Journal of the American Chemical Society p. 1675,1680 (1972)

Update date:2022-08-05

Topics:

Authors:

Gajewski

Shih Shih

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

Article abstract of DOI:10.1021/ja00760a041

Full text of DOI:10.1021/ja00760a041

Products guided by the article

Product name:1.2-Bis(tosyloxydideuteromethyl)cyclobutan

Cas No:35630-09-2

R&D Labs maybe for 35630-09-2

SHANDONG QINGYUNCHANGXIN CHEMICAL SCIENCE-TECH CO.,LTD

Contact:86-21-60560171

Address:1689Donghuan Rade,Qingyun County, Dezhou City, Shandong,China
Win-Win chemical Co.Ltd

website:http://www.win-winchemical.com

Contact:0086-577-64498589

Address:6F, No. 396 Xingping Road, Longwan Industrial Zone, Wenzhou City, Zhejiang, 325000 P.R.China
Shandong Xingshun New Material Co., Ltd.

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

Contact:+86-519-86461196/+86-519-86464994

Address:Middle of Luhua East Road, Dingtao District
Tianjin Dongchang Fine Chemical Industry Co., Ltd.

Contact:+86-22-29894595

Address:Economic Developing Zone, Ji County, Tianjin, China
Luzhou North Chemical Co., Ltd.

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

Address:Gaoba, Longmatan District, Luzhou, Sichuan Province

Relevant to this article

Syntheses and crystal structures of mononuclear rhodium hydrido complexes from the reactions of [RH(H)₂(PPH₃)₂(ETOH)₂] C1O₄ with various nitrogen ligands

Doi:10.1016/S0277-5387(02)01028-8
(2002)
Cross-functionalities of Bacillus deacetylases involved in bacillithiol biosynthesis and bacillithiol-S-conjugate detoxification pathways

Doi:10.1042/BJ20130415
(2013)
Reduction of carboxylic esters to ethers with triethyl silane in the combined use of titanium tetrachloride and trimethylsilyl trifluoromethanesulfonate

Doi:10.1016/S0040-4020(01)00420-3
(2001)
Doi:10.1007/BF00901236
(1968)
Doi:10.1039/jr9650005377
(1965)
Catalytic cycle for the asymmetric hydrogenation of prochiral ketones to chiral alcohols: Direct hydride and proton transfer from chiral catalysts trans-Ru(H)₂(diphosphine)(diamine) to ketones and direct addition of dihydrogen to the resulting

Doi:10.1021/ja015902u
(2001)

Article Doi

DOI: 10.1021/ja00760a041

Source and publish data: