Hydroxylated pyrrolizidines and indolizidines; syntheses using cycloaddition reactions of functionalized cyclic nitrones

A. E. McCaig, R. H. Wightman

Research output: Contribution to journalArticle

Abstract

Cycloaddition reactions of functionalised ?1-pyrroline-N-oxides have been used to prepare the hydroxylated pyrrolizidines 11 and 22, the indolizidine 16, and the iminoheptitol 12.

Original languageEnglish
Pages (from-to)3939-3942
Number of pages4
JournalTetrahedron Letters
Volume34
Issue number24
DOIs
Publication statusPublished - 1993

Fingerprint

Indolizidines
Cycloaddition
Oxides
nitrones
pyrroline

Cite this

@article{d546f4dbaaa449829c63286f1bae0ed2,
title = "Hydroxylated pyrrolizidines and indolizidines; syntheses using cycloaddition reactions of functionalized cyclic nitrones",
abstract = "Cycloaddition reactions of functionalised ?1-pyrroline-N-oxides have been used to prepare the hydroxylated pyrrolizidines 11 and 22, the indolizidine 16, and the iminoheptitol 12.",
author = "McCaig, {A. E.} and Wightman, {R. H.}",
year = "1993",
doi = "10.1016/S0040-4039(00)79269-0",
language = "English",
volume = "34",
pages = "3939--3942",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "24",

}

Hydroxylated pyrrolizidines and indolizidines; syntheses using cycloaddition reactions of functionalized cyclic nitrones. / McCaig, A. E.; Wightman, R. H.

In: Tetrahedron Letters, Vol. 34, No. 24, 1993, p. 3939-3942.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Hydroxylated pyrrolizidines and indolizidines; syntheses using cycloaddition reactions of functionalized cyclic nitrones

AU - McCaig, A. E.

AU - Wightman, R. H.

PY - 1993

Y1 - 1993

N2 - Cycloaddition reactions of functionalised ?1-pyrroline-N-oxides have been used to prepare the hydroxylated pyrrolizidines 11 and 22, the indolizidine 16, and the iminoheptitol 12.

AB - Cycloaddition reactions of functionalised ?1-pyrroline-N-oxides have been used to prepare the hydroxylated pyrrolizidines 11 and 22, the indolizidine 16, and the iminoheptitol 12.

UR - http://www.scopus.com/inward/record.url?scp=0027246057&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)79269-0

DO - 10.1016/S0040-4039(00)79269-0

M3 - Article

VL - 34

SP - 3939

EP - 3942

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 24

ER -