Scholarly article on 4,5-Dihydrothiepin 1,1-dioxide 29520-87-4 from Journal of the Chemical Society, Section D: Chemical Communications p. 313

DOI: 10.1039/c29710000313

Source and publish data:

Journal of the Chemical Society, Section D: Chemical Communications p. 313 (1971)

Update date:2022-07-27

Topics:

Authors:

Paquette

Maiorana

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

Article abstract of DOI:10.1039/c29710000313

Full text of DOI:10.1039/c29710000313

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

View Article Online

Products guided by the article

Product name:4,5-Dihydrothiepin 1,1-dioxide

Cas No:29520-87-4

R&D Labs maybe for 29520-87-4

Jiangsu Feymer Technology Co., Ltd.

Contact:+86-512-58110132

Address:Fenghuang Town, Zhangjiagang City, Jiangsu Province, China
CHEMINN LTD.

website:http://www.cheminn.com/

Contact:86-531-67875205

Address:No.9-2,South of Shanda Road, Jinan ,China
Maithili Life Sciences

Contact:+91 9963263336

Address:Plot#146A, IDA Mallapur, Hyderabad - 500072
Huaian Double Win Chemicals Co.,Ltd.

Contact:+86-13511538872

Address:Blk 43,Greenland Century Town,Huaian District, Huaian City,Jiangsu Province,China
HANGZHOU FOREWIN PHARMA CO., LTD

Contact:+86-571-89053961

Address:hangzhou

Relevant to this article

Doi:10.1016/S0040-4039(00)76154-5
(1968)
The effect of phenyl substituents on the release rates of esterase-sensitive coumarin-based prodrugs

Doi:10.1248/cpb.48.1138
(2000)
1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 4: Synthesis of N-1 acidic functionality affording analogues with enhanced antiviral activity against HIV

Doi:10.1016/S0960-894X(02)00606-6
(2002)
Aromatic ring opening of fused thiophenes via organolithium addition to sulfur

Doi:10.1055/s-1998-1674
(1998)
Synthesis of the C15-C27 fragment of the antitumor agent laulimalide

Doi:10.1016/S0040-4039(00)00961-8
(2000)
Synthesis of carboxamide and sulfonyl carboxamide linked heterocycles under green conditions

Doi:10.24820/ark.5550190.p010.820
(2019)

Article Doi

DOI: 10.1039/c29710000313