An alternative total synthesis of rutaecarpine and vasicolinone alkaloids

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

Rutaecarpine (6) and vasicolinone (9) alkaloids were alternatively prepared by Fischer indolization of 3-(phenylhydrazonomethyl)pyrroloquinazoline (4) under thermal and acidic conditions, respectively.

Original languageEnglish
Pages (from-to)2995-2998
Number of pages4
JournalTetrahedron Letters
Volume33
Issue number21
DOIs
Publication statusPublished - May 19 1992

Fingerprint

Alkaloids
Hot Temperature
rutecarpine

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

An alternative total synthesis of rutaecarpine and vasicolinone alkaloids. / Kökösi, J.; Szász, G.; Hermecz, I.

In: Tetrahedron Letters, Vol. 33, No. 21, 19.05.1992, p. 2995-2998.

Research output: Contribution to journalArticle

@article{872d948101ab4d06bd7786cbda6bbb17,
title = "An alternative total synthesis of rutaecarpine and vasicolinone alkaloids",
abstract = "Rutaecarpine (6) and vasicolinone (9) alkaloids were alternatively prepared by Fischer indolization of 3-(phenylhydrazonomethyl)pyrroloquinazoline (4) under thermal and acidic conditions, respectively.",
author = "J. K{\"o}k{\"o}si and G. Sz{\'a}sz and I. Hermecz",
year = "1992",
month = "5",
day = "19",
doi = "10.1016/S0040-4039(00)79581-5",
language = "English",
volume = "33",
pages = "2995--2998",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "21",

}

TY - JOUR

T1 - An alternative total synthesis of rutaecarpine and vasicolinone alkaloids

AU - Kökösi, J.

AU - Szász, G.

AU - Hermecz, I.

PY - 1992/5/19

Y1 - 1992/5/19

N2 - Rutaecarpine (6) and vasicolinone (9) alkaloids were alternatively prepared by Fischer indolization of 3-(phenylhydrazonomethyl)pyrroloquinazoline (4) under thermal and acidic conditions, respectively.

AB - Rutaecarpine (6) and vasicolinone (9) alkaloids were alternatively prepared by Fischer indolization of 3-(phenylhydrazonomethyl)pyrroloquinazoline (4) under thermal and acidic conditions, respectively.

UR - http://www.scopus.com/inward/record.url?scp=0026683553&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0026683553&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)79581-5

DO - 10.1016/S0040-4039(00)79581-5

M3 - Article

VL - 33

SP - 2995

EP - 2998

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 21

ER -