Alkylation of 2-phenylsulfinylethanol

Ohta Hiromichi; Matsumoto Shinsuke; Sugai Takeshi

doi:10.1016/0040-4039(90)80177-N

Alkylation of 2-phenylsulfinylethanol

Ohta Hiromichi, Matsumoto Shinsuke, Sugai Takeshi

School of Pharmaceutical Sciences

Research output: Contribution to journal › Article › peer-review

3 Citations (Scopus)

Abstract

Alkylation of 2-phenylsulfinylethanol resulted syndiastereomer as the major products, although the ratio of syn/anti isomers varied depending on the alkyl groups. By application of this procedure to the chiral sulfoxides, optically active epoxides have been obtained in good yields.

Original language	English
Pages (from-to)	2895-2898
Number of pages	4
Journal	Tetrahedron Letters
Volume	31
Issue number	20
DOIs	https://doi.org/10.1016/0040-4039(90)80177-N
Publication status	Published - 1990

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/0040-4039(90)80177-N

Cite this

@article{448b6a3eea994e46a39574d11793b1c4,

title = "Alkylation of 2-phenylsulfinylethanol",

abstract = "Alkylation of 2-phenylsulfinylethanol resulted syndiastereomer as the major products, although the ratio of syn/anti isomers varied depending on the alkyl groups. By application of this procedure to the chiral sulfoxides, optically active epoxides have been obtained in good yields.",

author = "Ohta Hiromichi and Matsumoto Shinsuke and Sugai Takeshi",

year = "1990",

doi = "10.1016/0040-4039(90)80177-N",

language = "English",

volume = "31",

pages = "2895--2898",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "20",

}

TY - JOUR

T1 - Alkylation of 2-phenylsulfinylethanol

AU - Hiromichi, Ohta

AU - Shinsuke, Matsumoto

AU - Takeshi, Sugai

PY - 1990

Y1 - 1990

N2 - Alkylation of 2-phenylsulfinylethanol resulted syndiastereomer as the major products, although the ratio of syn/anti isomers varied depending on the alkyl groups. By application of this procedure to the chiral sulfoxides, optically active epoxides have been obtained in good yields.

AB - Alkylation of 2-phenylsulfinylethanol resulted syndiastereomer as the major products, although the ratio of syn/anti isomers varied depending on the alkyl groups. By application of this procedure to the chiral sulfoxides, optically active epoxides have been obtained in good yields.

UR - http://www.scopus.com/inward/record.url?scp=0025339994&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0025339994&partnerID=8YFLogxK

U2 - 10.1016/0040-4039(90)80177-N

DO - 10.1016/0040-4039(90)80177-N

M3 - Article

AN - SCOPUS:0025339994

SN - 0040-4039

VL - 31

SP - 2895

EP - 2898

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 20

ER -

Alkylation of 2-phenylsulfinylethanol

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this