Phosphabarrelene-modified Rh-catalysts: a new and selective route towards hydroxy-functionalized bicyclic imidazoles via tandem reactions

P.S. Bäuerlein; I. Arenas Gonzalez; J.J.M. Weemers; M. Lutz; A.L. Spek; D. Vogt; Christian Müller

Phosphabarrelene-modified Rh-catalysts: a new and selective route towards hydroxy-functionalized bicyclic imidazoles via tandem reactions

P.S. Bäuerlein, I. Arenas Gonzalez, J.J.M. Weemers, M. Lutz, A.L. Spek, D. Vogt, Christian Müller

Sub Crystal and Structural Chemistry

extern

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

Abstract

8-Hydroxy-6-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine was formed selectively in high yields from N-(b-methallyl)imidazole by a tandem hydroformylation–cyclization sequence, representing a novel one-pot catalytic synthesis of bicyclic imidazole derivatives.

Original language	Undefined/Unknown
Pages (from-to)	4944-4946
Number of pages	3
Journal	Chemical Communications
Volume	2009
Issue number	33
Publication status	Published - 2009

Embargoed Document

B911612e
Final published version, 1.16 MB
Embargo ends: 1/01/50
Request copy

Cite this

@article{5958a59aace4446785407475dfa788fd,

title = "Phosphabarrelene-modified Rh-catalysts: a new and selective route towards hydroxy-functionalized bicyclic imidazoles via tandem reactions",

abstract = "8-Hydroxy-6-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine was formed selectively in high yields from N-(b-methallyl)imidazole by a tandem hydroformylation–cyclization sequence, representing a novel one-pot catalytic synthesis of bicyclic imidazole derivatives.",

author = "P.S. B{\"a}uerlein and {Arenas Gonzalez}, I. and J.J.M. Weemers and M. Lutz and A.L. Spek and D. Vogt and Christian M{\"u}ller",

year = "2009",

language = "Undefined/Unknown",

volume = "2009",

pages = "4944--4946",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "33",

}

TY - JOUR

T1 - Phosphabarrelene-modified Rh-catalysts: a new and selective route towards hydroxy-functionalized bicyclic imidazoles via tandem reactions

AU - Bäuerlein, P.S.

AU - Arenas Gonzalez, I.

AU - Weemers, J.J.M.

AU - Lutz, M.

AU - Spek, A.L.

AU - Vogt, D.

AU - Müller, Christian

PY - 2009

Y1 - 2009

N2 - 8-Hydroxy-6-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine was formed selectively in high yields from N-(b-methallyl)imidazole by a tandem hydroformylation–cyclization sequence, representing a novel one-pot catalytic synthesis of bicyclic imidazole derivatives.

AB - 8-Hydroxy-6-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine was formed selectively in high yields from N-(b-methallyl)imidazole by a tandem hydroformylation–cyclization sequence, representing a novel one-pot catalytic synthesis of bicyclic imidazole derivatives.

M3 - Article

SN - 1359-7345

VL - 2009

SP - 4944

EP - 4946

JO - Chemical Communications

JF - Chemical Communications

IS - 33

ER -