NaH-mediated iodoaziridination reaction of N-allylic tosylamides

Osamu Kitagawa, Takashi Suzuki, Takeo Taguchi

Research output: Contribution to journalArticle

12 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 languageEnglish
Pages (from-to)8371-8374
Number of pages4
JournalTetrahedron Letters
Volume38
Issue number48
Publication statusPublished - 1997 Dec 1
Externally publishedYes

Fingerprint

Derivatives

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

NaH-mediated iodoaziridination reaction of N-allylic tosylamides. / Kitagawa, Osamu; Suzuki, Takashi; Taguchi, Takeo.

In: Tetrahedron Letters, Vol. 38, No. 48, 01.12.1997, p. 8371-8374.

Research output: Contribution to journalArticle

Kitagawa, O, Suzuki, T & Taguchi, T 1997, 'NaH-mediated iodoaziridination reaction of N-allylic tosylamides', Tetrahedron Letters, vol. 38, no. 48, pp. 8371-8374.
Kitagawa, Osamu ; Suzuki, Takashi ; Taguchi, Takeo. / NaH-mediated iodoaziridination reaction of N-allylic tosylamides. In: Tetrahedron Letters. 1997 ; Vol. 38, No. 48. pp. 8371-8374.
@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 = "12",
day = "1",
language = "English",
volume = "38",
pages = "8371--8374",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "48",

}

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

M3 - Article

AN - SCOPUS:0030703149

VL - 38

SP - 8371

EP - 8374

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 48

ER -