A study of Heck cyclization reactions to form phenanthridine ring systems

L.R. Donaldson; David Haigh; A.N. Hulme

doi:10.1016/j.tet.2008.02.044

A study of Heck cyclization reactions to form phenanthridine ring systems

L.R. Donaldson, David Haigh, A.N. Hulme

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

21 Citations (Scopus)

Abstract

A survey of conditions for the palladium catalyzed intramol. Heck cyclization of protected amines has shown that the Herrmann-Beller palladacycle can be exploited under 'cationic' conditions to provide a robust and rapid route (

Original language	English
Pages (from-to)	4468-4477
Number of pages	10
Journal	Tetrahedron
Volume	64
Issue number	19
DOIs	https://doi.org/10.1016/j.tet.2008.02.044
Publication status	Published - 05 May 2008

ASJC Scopus subject areas

Biochemistry
Organic Chemistry
Drug Discovery

Access to Document

10.1016/j.tet.2008.02.044

Cite this

@article{86c7f589c9754522b45cebc5939547ff,

title = "A study of Heck cyclization reactions to form phenanthridine ring systems",

abstract = "A survey of conditions for the palladium catalyzed intramol. Heck cyclization of protected amines has shown that the Herrmann-Beller palladacycle can be exploited under 'cationic' conditions to provide a robust and rapid route (",

author = "L.R. Donaldson and David Haigh and A.N. Hulme",

year = "2008",

month = may,

day = "5",

doi = "10.1016/j.tet.2008.02.044",

language = "English",

volume = "64",

pages = "4468--4477",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier Ltd",

number = "19",

}

TY - JOUR

T1 - A study of Heck cyclization reactions to form phenanthridine ring systems

AU - Donaldson, L.R.

AU - Haigh, David

AU - Hulme, A.N.

PY - 2008/5/5

Y1 - 2008/5/5

N2 - A survey of conditions for the palladium catalyzed intramol. Heck cyclization of protected amines has shown that the Herrmann-Beller palladacycle can be exploited under 'cationic' conditions to provide a robust and rapid route (

AB - A survey of conditions for the palladium catalyzed intramol. Heck cyclization of protected amines has shown that the Herrmann-Beller palladacycle can be exploited under 'cationic' conditions to provide a robust and rapid route (

UR - http://www.scopus.com/inward/record.url?scp=41549166001&partnerID=8YFLogxK

U2 - 10.1016/j.tet.2008.02.044

DO - 10.1016/j.tet.2008.02.044

M3 - Article

SN - 0040-4020

VL - 64

SP - 4468

EP - 4477

JO - Tetrahedron

JF - Tetrahedron

IS - 19

ER -

A study of Heck cyclization reactions to form phenanthridine ring systems

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this