1,2-Dithiines and precursors, XVI: Synthesis, structure, and reactivity of non-anellated 1,2-dithiines

DOI: 10.1016/0040-4020(96)00752-1

Source and publish data:

Tetrahedron p. 12677 - 12698 (1996)

Update date:2022-08-05

Topics:

Authors:

Schroth, Werner

Dunger, Simona

Billig, Frank

Spitzner, Roland

Herzschuh, Rainer

Vogt, Almut

Jende, Thomas

Israel, Gunter

Barche, Jens

Stroehl, Dieter

Sieler, Joachim

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

Article abstract of DOI:10.1016/0040-4020(96)00752-1

Various monocyclic 1,2-dithiines 6a,b,d-t were prepared via (Z,Z)-1,4-difunctionalized butadienes (4-11,19,20). A twisted cyclic structure A is unequivocally proved rather than of the ringopened valence isomer B. The reactivity of these 1,2-dithiines is d

Full text of DOI:10.1016/0040-4020(96)00752-1

Products guided by the article

Product name:(Z,Z)-1,4-di(t-butylthio)-1,4-di(p-tolyl)-1,3-butadiene

Cas No:183211-02-1

R&D Labs maybe for 183211-02-1

Suzhou Time-chem Technologies Co., Ltd.

Contact:0512-63983931/68086856

Address:No. 1326 of Binhe Road, New District, Suzhou, Jiangsu, P. R. China
Tianjin Tongde Biological Technology Co., Ltd.

Contact:86-22-23309138

Address:Room 402, bulidingE3 Detection certification park, XiQingDistrict, Tianjin City
HENAN NEW BLUE CHEMICAL CO.,LTD

website:http://www.newbluechem.com

Contact:86-371-55170693/55170694

Address:Zhengzhou International Trade New Territory,Jinshui District,Zhengzhou ,China
Hangzhou Neway Chemicals Co., Ltd.

Contact:+86-571-85095566

Address:Room 803, Qinglian Bldg, No 139 Qingchun Road, Hangzhou, Zhejiang China
henan victory industry co.ltd

Contact:86-371-63655023

Address:No.85,jinshui road,zhengzhou,China

Relevant to this article

Hydrophobic effects in duplexes with modified oligonucleotide backbones and RNA

Doi:10.1016/0960-894X(96)00434-9
(1996)
Doi:10.1021/jo01254a040
(1969)
Studies on the reaction of phenyl glycidyl ether with alcohols or thiols

Doi:10.1248/yakushi1947.88.1_21
(1968)
Merging supramolecular catalysis and aminocatalysis: Amino-appended β-cyclodextrins (ACDs) as efficient and recyclable supramolecular catalysts for the synthesis of tetraketones

Doi:10.1039/c6ra01002d
(2016)
Generalizing glycosylation: Synthesis of the blood group antigens Le^a, Le^b, and Le(x) using a standard set of reaction conditions

Doi:10.1021/ja9608555
(1996)
Michael reaction in the solid state under microwave irradiations

Doi:10.1246/cl.1996.965
(1996)

Article Doi