NaH-mediated iodoaziridination reaction of N-allylic tosylamides

Osamu Kitagawa; Takashi Suzuki; Takeo Taguchi

doi:10.1016/S0040-4039(97)10271-4

NaH-mediated iodoaziridination reaction of N-allylic tosylamides

Osamu Kitagawa, Takashi Suzuki, Takeo Taguchi

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

15 Citations (Scopus)

Abstract

In the presence of NaH and I₂, iodocyclization reaction of N-allylic tosylamide derivatives proceeds in a highly stereospecific trans-addition manner to give good yields of iodoaziridines.

Original language	English
Pages (from-to)	8371-8374
Number of pages	4
Journal	Tetrahedron Letters
Volume	38
Issue number	48
DOIs	https://doi.org/10.1016/S0040-4039(97)10271-4
Publication status	Published - 1997 Dec 1
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(97)10271-4

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@article{3350ae2e52b148198500ecf0379d484b,

title = "NaH-mediated iodoaziridination reaction of N-allylic tosylamides",

abstract = "In the presence of NaH and I2, iodocyclization reaction of N-allylic tosylamide derivatives proceeds in a highly stereospecific trans-addition manner to give good yields of iodoaziridines.",

author = "Osamu Kitagawa and Takashi Suzuki and Takeo Taguchi",

year = "1997",

month = dec,

day = "1",

doi = "10.1016/S0040-4039(97)10271-4",

language = "English",

volume = "38",

pages = "8371--8374",

journal = "Tetrahedron Letters",

issn = "0040-4039",

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TY - JOUR

T1 - NaH-mediated iodoaziridination reaction of N-allylic tosylamides

AU - Kitagawa, Osamu

AU - Suzuki, Takashi

AU - Taguchi, Takeo

PY - 1997/12/1

Y1 - 1997/12/1

N2 - In the presence of NaH and I2, iodocyclization reaction of N-allylic tosylamide derivatives proceeds in a highly stereospecific trans-addition manner to give good yields of iodoaziridines.

AB - In the presence of NaH and I2, iodocyclization reaction of N-allylic tosylamide derivatives proceeds in a highly stereospecific trans-addition manner to give good yields of iodoaziridines.

UR - http://www.scopus.com/inward/record.url?scp=0030703149&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0030703149&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(97)10271-4

DO - 10.1016/S0040-4039(97)10271-4

M3 - Article

AN - SCOPUS:0030703149

SN - 0040-4039

VL - 38

SP - 8371

EP - 8374

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 48

ER -

NaH-mediated iodoaziridination reaction of N-allylic tosylamides

Abstract

ASJC Scopus subject areas

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