Imido transfer of sulfonylimino-λ3-bromane makes possible the synthesis of sulfonylimino-λ3-iodanes

Masahito Ochiai; Aiko Nakano; Akira Yoshimura; Kazunori Miyamoto; Satoko Hayashi; Waro Nakanishi

doi:10.1039/b818489e

Imido transfer of sulfonylimino-λ³-bromane makes possible the synthesis of sulfonylimino-λ³-iodanes

Masahito Ochiai
, Aiko Nakano
, Akira Yoshimura
, Kazunori Miyamoto
, Satoko Hayashi
, Waro Nakanishi

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

21 Scopus citations

Abstract

Sulfonylimino-λ³-bromane functions as a reactive nitrenoid, because of the hyperleaving group ability of aryl- λ³-bromanyl groups, and undergoes transimidations to iodobenzenes at room temperature under metal-free conditions probably via an S_N2-type nitrenoid transition state, yielding sulfonylimino- λ³-iodanes.

Original language	English (US)
Pages (from-to)	959-961
Number of pages	3
Journal	Chemical Communications
Issue number	8
DOIs	https://doi.org/10.1039/b818489e
State	Published - 2009
Externally published	Yes

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10.1039/b818489e

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title = "Imido transfer of sulfonylimino-λ3-bromane makes possible the synthesis of sulfonylimino-λ3-iodanes",

abstract = "Sulfonylimino-λ3-bromane functions as a reactive nitrenoid, because of the hyperleaving group ability of aryl- λ3-bromanyl groups, and undergoes transimidations to iodobenzenes at room temperature under metal-free conditions probably via an SN2-type nitrenoid transition state, yielding sulfonylimino- λ3-iodanes.",

author = "Masahito Ochiai and Aiko Nakano and Akira Yoshimura and Kazunori Miyamoto and Satoko Hayashi and Waro Nakanishi",

year = "2009",

doi = "10.1039/b818489e",

language = "English (US)",

pages = "959--961",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "8",

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TY - JOUR

T1 - Imido transfer of sulfonylimino-λ3-bromane makes possible the synthesis of sulfonylimino-λ3-iodanes

AU - Ochiai, Masahito

AU - Nakano, Aiko

AU - Yoshimura, Akira

AU - Miyamoto, Kazunori

AU - Hayashi, Satoko

AU - Nakanishi, Waro

PY - 2009

Y1 - 2009

N2 - Sulfonylimino-λ3-bromane functions as a reactive nitrenoid, because of the hyperleaving group ability of aryl- λ3-bromanyl groups, and undergoes transimidations to iodobenzenes at room temperature under metal-free conditions probably via an SN2-type nitrenoid transition state, yielding sulfonylimino- λ3-iodanes.

AB - Sulfonylimino-λ3-bromane functions as a reactive nitrenoid, because of the hyperleaving group ability of aryl- λ3-bromanyl groups, and undergoes transimidations to iodobenzenes at room temperature under metal-free conditions probably via an SN2-type nitrenoid transition state, yielding sulfonylimino- λ3-iodanes.

UR - https://www.scopus.com/pages/publications/61449108108

UR - https://www.scopus.com/pages/publications/61449108108#tab=citedBy

U2 - 10.1039/b818489e

DO - 10.1039/b818489e

M3 - Article

C2 - 19214329

AN - SCOPUS:61449108108

SN - 1359-7345

SP - 959

EP - 961

JO - Chemical Communications

JF - Chemical Communications

IS - 8

ER -

Imido transfer of sulfonylimino-λ³-bromane makes possible the synthesis of sulfonylimino-λ³-iodanes

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