Highly Selective Thioselenation of Olefins Using Disulfide-Diselenide Mixed System

DOI: 10.1021/jo00027a021

Source and publish data:

Journal of Organic Chemistry p. 111 - 115 (1992)

Update date:2022-07-30

Topics:

Authors:

Ogawa, Akiya

Tanaka, Hiromichi

Yokoyama, Hiroshi

Obayashi, Ryoichi

Yokoyama, Kazuyuki

Sonoda, Noboru

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

Article abstract of DOI:10.1021/jo00027a021

A highly selective thioselenation of olefins has been attained by using s disulfide-diselenide mixed system.Upon irradiation through Pyrex with a tungsten lamp in the absence of solvent, the thioselenation of olefins 1 with diphenyl disulfide (2) and diph

Full text of DOI:10.1021/jo00027a021

Products guided by the article

Product name:1-exo-(Phenylthio)-2-exo-(phenylseleno)norbornane

Cas No:137429-16-4

R&D Labs maybe for 137429-16-4

Changzhou Welton Chemical Co., Ltd,

Contact:0086-519-85910828,85920537,85912897

Address:No.8 Jinlong Road, Binjiang Park, Changzhou, Jiangsu, China.
ZHUHAI HAIRUIDE BIOSCIENCE AND TECHNOLOGY CO.,LTD

website:http://www.zhhairuide.com

Contact:+8613326687259/+86-756-7789199

Address:No.10 Yonghui Road
Jinan Baozhao Pharmaceutical Co., Ltd

Contact:0086-531-86397156 82371858 82371868

Address:Huaneng Road, Jinan, Shandong ,China
Beijing Apis Biotechnology Co., Ltd.

Contact:86-010-67856775-8551

Address:NO.4PUHUANGYU ROAD,FENTAI DISTRICT, BEIJING, CHINA
Dongtai Xinyuan Chemical Co., Ltd.

Contact:+86-21-56733000

Address:404F, 99Nong No.117 Zhongtan Rd. Shanghai

Relevant to this article

Asymmetric CONJUGATE ADDITION of MALONATE ESTERS to α,β- UNSATURATED N-sulfonyl imines: An expeditious route to chiral δ-aminoesters and piperidones

Doi:10.1002/chem.201302687
(2013)
FeCl₃·6H₂O and TfOH as catalysts for allylic amination reaction: A comparative study

Doi:10.1002/ejoc.201101844
(2012)
Efficient preparation of α-aminoboronic acid derivatives via boroalkyl group migration

Doi:10.1055/s-0033-1340502
(2014)
Concise Synthesis of a Potential 5-Lipoxygenase Activating Protein (FLAP) Inhibitor and Its Analogs through Late-Stage Alkene Dicarbofunctionalization

Doi:10.1021/acs.oprd.9b00199
(2019)
Asymmetric Michael addition of boronic acids to a γ-hydroxy-α, β-unsaturated aldehyde catalyzed by resin-supported peptide

Doi:10.1039/c2ob25431j
(2012)
Design, synthesis and bioevaluation of novel 6-(4-Hydroxypiperidino)naphthalen-2-ol-based potential selective estrogen receptor modulators for breast cancer

Doi:10.1016/j.ejmech.2014.12.037
(2015)

Article Doi