Facile one-pot synthesis of α-chloro sulfoxides from sulfides

DOI: 10.1055/s-1993-25831

Source and publish data:

Synthesis p. 209 - 210 (1993)

Update date:2022-08-04

Topics:

Authors:

Kim Kim

Shin Shin

Park Park

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

Article abstract of DOI:10.1055/s-1993-25831

Various sulfides 1 reacted with sulfuryl chloride in the presence of metal nitrates in acetonitrile under mild conditions to give the corresponding α-chloro sulfoxides 2 in good yields.

Full text of DOI:10.1055/s-1993-25831

Products guided by the article

Product name:1-bromo-4-(chloromethylsulfonyl)benzene

Cas No:67833-42-5

R&D Labs maybe for 67833-42-5

SJZ THLD IMP & EXP CO LTD

website:http://www.truewingroup.com

Contact:86-311-66699812

Address:NO.600 ZHONGSHAN EAST ROAD SHIJIAZHUANG
Ningbo J&S Botanics Inc.

Contact:86-574-26865651

Address:529 YuanBaoShan Road, Beilun District
ClickChem Technology Co., Limited

Contact:+86-0310-6519966/0531-52893837

Address:No.750 Shunhua Road, High-Tech Zone, Jinan city, Shandong China
Shanghai WinTide BioTechnology Co.,Ltd

Contact:86-21-37100630

Address:No. 908 Yunhe Road, Fengxian district, Shanghai
LIANYUNGANG YC FINE CHEMICAL CO., LTD

Contact:+86-518-858 99188

Address:Shangdong Modern Bldg, South Greenpark Road, Lianyungang, Jiangsu Pro. China

Relevant to this article

SINTHESIS AND PROPERTIES OF PYRIMIDINYLALKYLSULFONAMIDES 5. REACTION OF Na SALT OF p-TOLUENESULFONAMIDE WITH SOME N-(ω-BROMOALKYL)URACILS, DEVOID OF GROUPINGS CAPABLE OF TAUTOMERISM IN THE PYRIMIDINE RING

Doi:10.1007/BF00951234
(1980)
Asymmetric 13-dipolar cycloaddition of nitrones with ketene acetals catalyzed by chiral oxazaborolidines

Doi:10.1016/S0040-4039(00)73373-9
(1994)
Doi:10.1016/S0022-328X(00)84871-8
(1978)
Doi:10.1021/jo00419a049
(1978)
Self-Assembly of Interlocked Supramolecular Dendrimers

Doi:10.1021/jo035798u
(2004)
The reactions of 2-hydroxypyridine ligands with Re₂Cl ₄(μ-dppm)₂ (dppm=Ph₂PCH₂PPh ₂) that lead to 2-pyridonate complexes

Doi:10.1016/j.ica.2003.06.018
(2004)

Article Doi