An efficient preparation of 1-phenylsulfonylindolyl methyl sulfoxides using KF/m-CPBA

Arasambattu K. Mohanakrishnan; Neelamegam Ramesh

doi:10.1016/j.tetlet.2005.04.067

An efficient preparation of 1-phenylsulfonylindolyl methyl sulfoxides using KF/m-CPBA

Arasambattu K. Mohanakrishnan, Neelamegam Ramesh

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

13 Scopus citations

Abstract

A variety of 1-phenylsulfonylindolylmethyl sulfides are selectively oxidized to the corresponding sulfoxides using a hitherto unexplored KF/m-CPBA system. A major advantage is the absence of over-oxidation.

Original language	English (US)
Pages (from-to)	4231-4233
Number of pages	3
Journal	Tetrahedron Letters
Volume	46
Issue number	24
DOIs	https://doi.org/10.1016/j.tetlet.2005.04.067
State	Published - Jun 13 2005
Externally published	Yes

Keywords

Indolylmethyl sulfide
Indolylmethyl sulfoxides
KF/m-CPBA
Sulfoxidation

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/j.tetlet.2005.04.067

Cite this

@article{74c639243b1f4f92a47313902241f639,

title = "An efficient preparation of 1-phenylsulfonylindolyl methyl sulfoxides using KF/m-CPBA",

abstract = "A variety of 1-phenylsulfonylindolylmethyl sulfides are selectively oxidized to the corresponding sulfoxides using a hitherto unexplored KF/m-CPBA system. A major advantage is the absence of over-oxidation.",

keywords = "Indolylmethyl sulfide, Indolylmethyl sulfoxides, KF/m-CPBA, Sulfoxidation",

author = "Mohanakrishnan, {Arasambattu K.} and Neelamegam Ramesh",

note = "Funding Information: A.K.M. thanks the UGC (F.12-140/2001 SR-1), New Delhi, for financial support. Financial support to the Department from DST-FIST is also acknowledged.",

year = "2005",

month = jun,

day = "13",

doi = "10.1016/j.tetlet.2005.04.067",

language = "English (US)",

volume = "46",

pages = "4231--4233",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "24",

}

TY - JOUR

T1 - An efficient preparation of 1-phenylsulfonylindolyl methyl sulfoxides using KF/m-CPBA

AU - Mohanakrishnan, Arasambattu K.

AU - Ramesh, Neelamegam

N1 - Funding Information: A.K.M. thanks the UGC (F.12-140/2001 SR-1), New Delhi, for financial support. Financial support to the Department from DST-FIST is also acknowledged.

PY - 2005/6/13

Y1 - 2005/6/13

N2 - A variety of 1-phenylsulfonylindolylmethyl sulfides are selectively oxidized to the corresponding sulfoxides using a hitherto unexplored KF/m-CPBA system. A major advantage is the absence of over-oxidation.

AB - A variety of 1-phenylsulfonylindolylmethyl sulfides are selectively oxidized to the corresponding sulfoxides using a hitherto unexplored KF/m-CPBA system. A major advantage is the absence of over-oxidation.

KW - Indolylmethyl sulfide

KW - Indolylmethyl sulfoxides

KW - KF/m-CPBA

KW - Sulfoxidation

UR - http://www.scopus.com/inward/record.url?scp=19044400897&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=19044400897&partnerID=8YFLogxK

U2 - 10.1016/j.tetlet.2005.04.067

DO - 10.1016/j.tetlet.2005.04.067

M3 - Article

AN - SCOPUS:19044400897

VL - 46

SP - 4231

EP - 4233

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 24

ER -

An efficient preparation of 1-phenylsulfonylindolyl methyl sulfoxides using KF/m-CPBA

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this