Synthesis of new phenyldiiodoalkyl sulfones

Victor H. Kesternich; Rolando Martinez; Pablo De-La-Rivera

Synthesis of new phenyldiiodoalkyl sulfones

Victor H. Kesternich, Rolando Martinez, Pablo De-La-Rivera

Facultad Ciencias Exactas

Resultado de la investigación: Contribución a una revista › Artículo › revisión exhaustiva

Resumen

A two-stage synthesis method has been developed to prepare phenyldiiodoalkyl sulfones. Unlike methods in the literature, isomers are not obtained and yield is better. In the first stage, iodoform reacted with thiophenol derivatives in order to generate the corresponding sulfides which, in the second stage, were oxidized with magnesium monoperphthalate (MMPP).

Idioma original	Inglés
Páginas (desde-hasta)	501-503
Número de páginas	3
Publicación	Boletin de la Sociedad Chilena de Quimica
Volumen	43
N.º	4
Estado	Publicada - 1 dic 1998

Áreas temáticas de ASJC Scopus

Química (todo)

Otros archivos y enlaces

Link to publication in Scopus

Citar esto

@article{acd0c670b660425eb178150d829353db,

title = "Synthesis of new phenyldiiodoalkyl sulfones",

abstract = "A two-stage synthesis method has been developed to prepare phenyldiiodoalkyl sulfones. Unlike methods in the literature, isomers are not obtained and yield is better. In the first stage, iodoform reacted with thiophenol derivatives in order to generate the corresponding sulfides which, in the second stage, were oxidized with magnesium monoperphthalate (MMPP).",

keywords = "Iodoalkylsulphones, Iodoform, Sulphones, Thiophenol",

author = "Kesternich, {Victor H.} and Rolando Martinez and Pablo De-La-Rivera",

year = "1998",

month = dec,

day = "1",

language = "English",

volume = "43",

pages = "501--503",

journal = "Journal of the Chilean Chemical Society",

issn = "0717-9324",

publisher = "Sociedad Chilena De Quimica",

number = "4",

}

TY - JOUR

T1 - Synthesis of new phenyldiiodoalkyl sulfones

AU - Kesternich, Victor H.

AU - Martinez, Rolando

AU - De-La-Rivera, Pablo

PY - 1998/12/1

Y1 - 1998/12/1

N2 - A two-stage synthesis method has been developed to prepare phenyldiiodoalkyl sulfones. Unlike methods in the literature, isomers are not obtained and yield is better. In the first stage, iodoform reacted with thiophenol derivatives in order to generate the corresponding sulfides which, in the second stage, were oxidized with magnesium monoperphthalate (MMPP).

AB - A two-stage synthesis method has been developed to prepare phenyldiiodoalkyl sulfones. Unlike methods in the literature, isomers are not obtained and yield is better. In the first stage, iodoform reacted with thiophenol derivatives in order to generate the corresponding sulfides which, in the second stage, were oxidized with magnesium monoperphthalate (MMPP).

KW - Iodoalkylsulphones

KW - Iodoform

KW - Sulphones

KW - Thiophenol

UR - http://www.scopus.com/inward/record.url?scp=33750104896&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:33750104896

VL - 43

SP - 501

EP - 503

JO - Journal of the Chilean Chemical Society

JF - Journal of the Chilean Chemical Society

SN - 0717-9324

IS - 4

ER -

Synthesis of new phenyldiiodoalkyl sulfones

Resumen

Áreas temáticas de ASJC Scopus

Otros archivos y enlaces

Huella

Citar esto