Reduction of α-Chlorocarbonyl Compounds by the Tributyltin Hydride-Phosphine Oxide Combined System. Chemoselective Reduction of the Carbonyl Group

DOI: 10.1039/c39880000882

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 882 - 883 (1988)

Update date:2022-07-30

Topics:

Authors:

Shibata, Ikuya

Suzuki, Taro

Baba, Akio

Matsuda, Haruo

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

Article abstract of DOI:10.1039/c39880000882

α-Chlorocarbonyl compounds undergo selective reduction at the carbonyl group with tributyltin hydride-phosphine oxide combined systems to yield chlorohydrins.

Full text of DOI:10.1039/c39880000882

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

View Article Online

Products guided by the article

Product name:2-chloro-3-phenyl-2-propen-1-ol

Cas No:23970-87-8

R&D Labs maybe for 23970-87-8

Jinan Jiaquan Chemical Co.,Ltd

Contact:+86-531-62318366

Address:Room 502 of Yidonghuayuan No.601 Huaxin Road Licheng District Jinan China
Puyang Huicheng Electronic Material Co., Ltd

website:http://huichengchem.weba.testwebsite.cn/index_en.html

Contact:+86-393-8910800

Address:West Section Shengli Road, Puyang457000, China
Hebei Fulong Import & Export Co., Ltd.

Contact:86-311-87795661

Address:15A19 Zhongyuan Building,368 Youyi North Street,Shijiazhuang 050070,China
Buffett (China) Holding Co.,Ltd

Contact:4006570891

Address:
Hangzhou Donglou Bio-nutrient Co., Ltd.

Contact:+86-571-82225795,13967112289

Address:Louta Town, Xiaoshan,Hangzhou,Zhejiang

Relevant to this article

Doi:10.1021/jo01121a001
(1955)
Doi:10.1007/BF00475854
()
Regioselectivity of vinyl sulfone based 1,3-dipolar cycloaddition reactions with sugar azides by computational and experimental studies

Doi:10.1021/ol500461s
(2014)
Site-selectivity in TBADT-photocatalyzed C(sp³)H functionalization of saturated alcohols and alkanes

Doi:10.1246/cl.171068
(2018)
Nickel-catalyzed cyclization of α,ω-dienes: Formation vs. cleavage of C-C bonds

Doi:10.1039/b601631f
(2006)
Synthetic studies on virantmycin. 2. Total synthesis of unnatural (+)-virantmycin and determination of its absolute stereochemistry

Doi:10.1016/0040-4020(96)00608-4
(1996)

Article Doi