The efficient one-step chlorination of methylsulfanyl group on pyrimidine ring system with sulfuryl chloride

Young Jin Ham; Duck Hyung Lee; Hwan Geun Choi; Jung Mi Hah; Taebo Sim

doi:10.1016/j.tetlet.2010.06.056

The efficient one-step chlorination of methylsulfanyl group on pyrimidine ring system with sulfuryl chloride

Young Jin Ham, Duck Hyung Lee, Hwan Geun Choi, Jung Mi Hah, Taebo Sim

KU-KIST Graduate School of Converging Science and Technology

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

2 Citations (Scopus)

Abstract

A facile one-step transformation of methylsulfanyl and arylsulfanyl groups on pyrimidine ring system into the corresponding chloride group was achieved using sulfuryl chloride in acetonitrile/dichloromethane.

Original language	English
Pages (from-to)	4609-4611
Number of pages	3
Journal	Tetrahedron Letters
Volume	51
Issue number	35
DOIs	https://doi.org/10.1016/j.tetlet.2010.06.056
Publication status	Published - 2010 Sept 1

Bibliographical note

Funding Information:
This work was supported by KOSFFL (The Korea Scholarship Foundation for the Future Leaders) program.

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2010.06.056

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title = "The efficient one-step chlorination of methylsulfanyl group on pyrimidine ring system with sulfuryl chloride",

abstract = "A facile one-step transformation of methylsulfanyl and arylsulfanyl groups on pyrimidine ring system into the corresponding chloride group was achieved using sulfuryl chloride in acetonitrile/dichloromethane.",

author = "Ham, {Young Jin} and Lee, {Duck Hyung} and Choi, {Hwan Geun} and Hah, {Jung Mi} and Taebo Sim",

note = "Funding Information: This work was supported by KOSFFL (The Korea Scholarship Foundation for the Future Leaders) program. ",

year = "2010",

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doi = "10.1016/j.tetlet.2010.06.056",

language = "English",

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journal = "Tetrahedron Letters",

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T1 - The efficient one-step chlorination of methylsulfanyl group on pyrimidine ring system with sulfuryl chloride

AU - Ham, Young Jin

AU - Lee, Duck Hyung

AU - Choi, Hwan Geun

AU - Hah, Jung Mi

AU - Sim, Taebo

N1 - Funding Information: This work was supported by KOSFFL (The Korea Scholarship Foundation for the Future Leaders) program.

PY - 2010/9/1

Y1 - 2010/9/1

N2 - A facile one-step transformation of methylsulfanyl and arylsulfanyl groups on pyrimidine ring system into the corresponding chloride group was achieved using sulfuryl chloride in acetonitrile/dichloromethane.

AB - A facile one-step transformation of methylsulfanyl and arylsulfanyl groups on pyrimidine ring system into the corresponding chloride group was achieved using sulfuryl chloride in acetonitrile/dichloromethane.

UR - http://www.scopus.com/inward/record.url?scp=77955653370&partnerID=8YFLogxK

U2 - 10.1016/j.tetlet.2010.06.056

DO - 10.1016/j.tetlet.2010.06.056

M3 - Article

AN - SCOPUS:77955653370

SN - 0040-4039

VL - 51

SP - 4609

EP - 4611

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 35

ER -

The efficient one-step chlorination of methylsulfanyl group on pyrimidine ring system with sulfuryl chloride

Abstract

Bibliographical note

ASJC Scopus subject areas

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