Scholarly article on 1-Cyclohex-1-enylmethyl-5,6-dihydro-4H-1λ4-[1,3]dithiine 37677-19-3 from Journal of the Chemical Society. Chemical communications p. 757

DOI: 10.1039/c39720000757

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 757 (1972)

Update date:2022-08-04

Topics:

Authors:

Hunt Hunt

Lythgoc Lythgoc

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

Article abstract of DOI:10.1039/c39720000757

Full text of DOI:10.1039/c39720000757

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

View Article Online

Products guided by the article

Product name:1-Cyclohex-1-enylmethyl-5,6-dihydro-4H-1λ⁴-[1,3]dithiine

Cas No:37677-19-3

R&D Labs maybe for 37677-19-3

Wuxi D-Stone International Co., Ltd.

Contact:+86-510-82740567

Address:21F Hengtong Int'l Centre, 215Zhongshan Road, Wuxi, Jiangsu,China
Jiaxing Trustworthy Import And Export Co.,Ltd

Contact:+86-573-82030555

Address:Room 1202, Unit B, Charming plaza,No.1558 East Zhongshan Road , Jiaxing City, Zhejiang Province, China.
Hybio Pharmaceutica Co.,Ltd

Contact:+86 755 26588093

Address:No.9 Linkong West Street, Hengdian Street, Huangpi District, Wuhan City, China.
Ningxia Soochow Agrochemical Limited Company

Contact:(+86）0512 6320 8190

Address:wujiang
YingYing Pharmaceutical Co.,Ltd

Contact:86-18854126208

Address:55#, yingxiongshan road

Relevant to this article

Highly stereoselective asymmetric construction of an acyclic carbon skeleton having two adjacent alkyl substituents by Michael addition of optically active allenyltitaniums to alkylidenemalonates

Doi:10.1021/ol016652p
(2001)
Doi:10.1007/BF00487466
()
Chiral liquid crystalline compounds with a re-entrant SmA* phase

Doi:10.1039/c1jm12131f
(2011)
Synthesis of derivatives of 1,3,2-diazaphospholidin-4-ones and the corresponding 2-sulfides

Doi:10.1002/hc.1076
(2001)
Doi:10.1039/P19720001926
(1972)
Dearomatization of 3,5-dinitropyridines - an atom-efficient approach to fused 3-nitropyrrolidines

Doi:10.24820/ark.5550190.p010.185
(2017)

Article Doi

DOI: 10.1039/c39720000757