Novel synthesis of 4-arylsulfenyl-3-hydroxy-2-pyrone: One pot substitution-rearrangement-cyclization reaction of acetonide protected 4,5-dihydroxy-2-chloroglycidic ester by sodium arylthiolate

Takuzo Komiyama; Yutaka Takaguchi; Sadao Tsuboi

doi:10.3987/COM-05-S(K)60

Novel synthesis of 4-arylsulfenyl-3-hydroxy-2-pyrone: One pot substitution-rearrangement-cyclization reaction of acetonide protected 4,5-dihydroxy-2-chloroglycidic ester by sodium arylthiolate

Takuzo Komiyama, Yutaka Takaguchi, Sadao Tsuboi

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

4 Citations (Scopus)

Abstract

-Treatment of acetonide protected 4,5-dihydroxy-2-chloroglycidic ester with sodium arylthiolate gave 4-arylsulfenyl-3-hydroxy-2-pyrone in excellent to good yields in one pot.

Original language	English
Pages (from-to)	503-509
Number of pages	7
Journal	Heterocycles
Volume	66
Issue number	1
DOIs	https://doi.org/10.3987/COM-05-S(K)60
Publication status	Published - Dec 31 2005

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

Access to Document

10.3987/COM-05-S(K)60

Cite this

Novel synthesis of 4-arylsulfenyl-3-hydroxy-2-pyrone: One pot substitution-rearrangement-cyclization reaction of acetonide protected 4,5-dihydroxy-2-chloroglycidic ester by sodium arylthiolate. / Komiyama, Takuzo; Takaguchi, Yutaka; Tsuboi, Sadao.
In: Heterocycles, Vol. 66, No. 1, 31.12.2005, p. 503-509.

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

@article{a4056689219a4ad8ac3f1dff165d78ab,

title = "Novel synthesis of 4-arylsulfenyl-3-hydroxy-2-pyrone: One pot substitution-rearrangement-cyclization reaction of acetonide protected 4,5-dihydroxy-2-chloroglycidic ester by sodium arylthiolate",

abstract = "-Treatment of acetonide protected 4,5-dihydroxy-2-chloroglycidic ester with sodium arylthiolate gave 4-arylsulfenyl-3-hydroxy-2-pyrone in excellent to good yields in one pot.",

author = "Takuzo Komiyama and Yutaka Takaguchi and Sadao Tsuboi",

year = "2005",

month = dec,

day = "31",

doi = "10.3987/COM-05-S(K)60",

language = "English",

volume = "66",

pages = "503--509",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

number = "1",

}

TY - JOUR

T1 - Novel synthesis of 4-arylsulfenyl-3-hydroxy-2-pyrone

T2 - One pot substitution-rearrangement-cyclization reaction of acetonide protected 4,5-dihydroxy-2-chloroglycidic ester by sodium arylthiolate

AU - Komiyama, Takuzo

AU - Takaguchi, Yutaka

AU - Tsuboi, Sadao

PY - 2005/12/31

Y1 - 2005/12/31

N2 - -Treatment of acetonide protected 4,5-dihydroxy-2-chloroglycidic ester with sodium arylthiolate gave 4-arylsulfenyl-3-hydroxy-2-pyrone in excellent to good yields in one pot.

AB - -Treatment of acetonide protected 4,5-dihydroxy-2-chloroglycidic ester with sodium arylthiolate gave 4-arylsulfenyl-3-hydroxy-2-pyrone in excellent to good yields in one pot.

UR - http://www.scopus.com/inward/record.url?scp=33646560198&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=33646560198&partnerID=8YFLogxK

U2 - 10.3987/COM-05-S(K)60

DO - 10.3987/COM-05-S(K)60

M3 - Article

AN - SCOPUS:33646560198

SN - 0385-5414

VL - 66

SP - 503

EP - 509

JO - Heterocycles

JF - Heterocycles

IS - 1

ER -

Novel synthesis of 4-arylsulfenyl-3-hydroxy-2-pyrone: One pot substitution-rearrangement-cyclization reaction of acetonide protected 4,5-dihydroxy-2-chloroglycidic ester by sodium arylthiolate

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this