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

Patrick S. Bauerlein; Ismael Arenas Gonzalez; Jarno J. M. Weemers; Martin Lutz; Anthony L. Spek; Dieter Vogt; Christian Muller

doi:10.1039/b911612e

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

Patrick S. Bauerlein, Ismael Arenas Gonzalez, Jarno J. M. Weemers, Martin Lutz, Anthony L. Spek, Dieter Vogt, Christian Muller

Research output: Contribution to journal › Article › 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	English
Pages (from-to)	4944-4946
Number of pages	3
Journal	Chemical Communications
Issue number	33
DOIs	https://doi.org/10.1039/b911612e
Publication status	Published - 2009

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@article{2658361d982c40adb648bd92192cba34,

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 = "Bauerlein, \{Patrick S.\} and Gonzalez, \{Ismael Arenas\} and Weemers, \{Jarno J. M.\} and Martin Lutz and Spek, \{Anthony L.\} and Dieter Vogt and Christian Muller",

year = "2009",

doi = "10.1039/b911612e",

language = "English",

pages = "4944--4946",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "33",

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

AU - Bauerlein, Patrick S.

AU - Gonzalez, Ismael Arenas

AU - Weemers, Jarno J. M.

AU - Lutz, Martin

AU - Spek, Anthony L.

AU - Vogt, Dieter

AU - Muller, 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.

U2 - 10.1039/b911612e

DO - 10.1039/b911612e

M3 - Article

SN - 1359-7345

SP - 4944

EP - 4946

JO - Chemical Communications

JF - Chemical Communications

IS - 33

ER -

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

Abstract

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