Scholarly article on (1S,2R,4R)-1,4-Dimethyl-4-((S)-1-methyl-2-methylene-cyclopentyl)-cyclohexane-1,2-diol 65596-35-2 from Journal of the Chemical Society. Chemical communications p. 566 - 568

DOI: 10.1039/c39770000566

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 566 - 568 (1977)

Update date:2022-08-05

Topics:

Authors:

Matsuo,A.

Hayashi,S.

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

Article abstract of DOI:10.1039/c39770000566

Full text of DOI:10.1039/c39770000566

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:(1S,2R,4R)-1,4-Dimethyl-4-((S)-1-methyl-2-methylene-cyclopentyl)-cyclohexane-1,2-diol

Cas No:65596-35-2

R&D Labs maybe for 65596-35-2

Shandong Topscience Biotech Co., Ltd.

Contact:0633-2619278

Address:No. 98 Lanshan West Road, Lanshan District, Rizhao, Shandong Province, P.R. of China
Xiamen Kaijia Imp & Exp Co., Ltd.

Contact:86-592-5101177

Address:Room406 Luhui Building No. 65 Haitian Road Huli Xiamen,China.
SINFACHEM LIMITED

Contact:86-25-84683399

Address:605, Phoenix Herui Plaza, No.389, South Taiping Road, Nanjing, China 210002
LinHai Cina Chemical Co., LTD.

Contact:0576-85580989

Address:Pharma-chem zone,Duqiao,Linhai,Zhejiang,China
SHIJIAZHUANG AGERUO-BIOTECH CO.LTD

Contact:+86-130-2866-6699

Address:Huaian east Road 158

Relevant to this article

Doi:10.1021/jm00299a014
(1970)
An unexpected synthesis of novel oxygen-bridged 1,5-benzothiazepine derivatives and their reductive five-membered-ring opening

Doi:10.1007/s007060050320
(2000)
Reaction of methylpyrimidine derivatives with isoamyl nitrite

Doi:10.1248/yakushi1947.90.7_877
(1970)
Doi:10.1039/j39700001469
(1970)
Synthesis of a D,D- and L,D-heptose-containing hexasaccharide corresponding to a structure from Haemophilus ducreyi lipopolysaccharides

Doi:10.1016/S0957-4166(99)00554-6
(2000)
Radical cyclisation studies of β-nitroamines from the nitro-Mannich reaction

Doi:10.1016/j.tet.2018.06.022
(2018)

Article Doi

DOI: 10.1039/c39770000566