A synthesis of (-) supinidine and its regioisomer by intramolecular oxime olefin cycloaddition.

Alfred Hassner; Suddham Singh; Raman Sharma; Rakesh Maurya

doi:10.1016/s0040-4020(01)80375-6

A synthesis of (-) supinidine and its regioisomer by intramolecular oxime olefin cycloaddition.

Alfred Hassner, Suddham Singh, Raman Sharma, Rakesh Maurya

Department of Chemistry

Bar-Ilan University

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

34 Scopus citations

Abstract

A synthesis of (-) supinidine 1 and its regioisomer 2 from L-proline is described. The key step is a thermal intramolecular oxime-olefin cycloaddition; dimerization products resulting from intramolecular nitrone formation were also isolated.

Original language	English
Pages (from-to)	2317-2324
Number of pages	8
Journal	Tetrahedron
Volume	49
Issue number	11
DOIs	https://doi.org/10.1016/s0040-4020(01)80375-6
State	Published - 12 Mar 1993

Access to Document

10.1016/s0040-4020(01)80375-6

Cite this

@article{c0a5854925ac489eb0c1ebd17d0aee9c,

title = "A synthesis of (-) supinidine and its regioisomer by intramolecular oxime olefin cycloaddition.",

abstract = "A synthesis of (-) supinidine 1 and its regioisomer 2 from L-proline is described. The key step is a thermal intramolecular oxime-olefin cycloaddition; dimerization products resulting from intramolecular nitrone formation were also isolated.",

author = "Alfred Hassner and Suddham Singh and Raman Sharma and Rakesh Maurya",

year = "1993",

month = mar,

day = "12",

doi = "10.1016/s0040-4020(01)80375-6",

language = "אנגלית",

volume = "49",

pages = "2317--2324",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier Ltd.",

number = "11",

}

TY - JOUR

T1 - A synthesis of (-) supinidine and its regioisomer by intramolecular oxime olefin cycloaddition.

AU - Hassner, Alfred

AU - Singh, Suddham

AU - Sharma, Raman

AU - Maurya, Rakesh

PY - 1993/3/12

Y1 - 1993/3/12

N2 - A synthesis of (-) supinidine 1 and its regioisomer 2 from L-proline is described. The key step is a thermal intramolecular oxime-olefin cycloaddition; dimerization products resulting from intramolecular nitrone formation were also isolated.

AB - A synthesis of (-) supinidine 1 and its regioisomer 2 from L-proline is described. The key step is a thermal intramolecular oxime-olefin cycloaddition; dimerization products resulting from intramolecular nitrone formation were also isolated.

UR - https://www.scopus.com/pages/publications/0027500354

U2 - 10.1016/s0040-4020(01)80375-6

DO - 10.1016/s0040-4020(01)80375-6

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???

AN - SCOPUS:0027500354

SN - 0040-4020

VL - 49

SP - 2317

EP - 2324

JO - Tetrahedron

JF - Tetrahedron

IS - 11

ER -

A synthesis of (-) supinidine and its regioisomer by intramolecular oxime olefin cycloaddition.

Abstract

Access to Document

Other files and links

Fingerprint

Cite this