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Your search keyword '"Munday, Rachel"' showing total 4 results
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4 results on '"Munday, Rachel"'

1. Asymmetric synthesis of 6'-hydroxyarenarol: the proposed biosynthetic precursor to popolohuanone E

Author

Munday, Rachel H., Denton, Ross M., and Anderson, James C.

Subjects
Dibenzofurans -- Chemical properties, Dibenzofurans -- Structure, Iodides -- Chemical properties, Oxidation-reduction reaction -- Analysis, Biological sciences, Chemistry
Abstract

Study presents the first synthesis of of (+)-6'-hydroxyarenarol, the proposed biogenetic precursor to popolohuanone E. An enantioselective route to key iodide intermediate is developed.

Published
2008

2. Palladium-catalyzed method for the synthesis of carbazoles via tandem C-H functionalization and C-N bond formation

Author

Tsang, W.C. Peter, Munday, Rachel H., Brasche, Gordon, Nan Zheng, and Buchwald, Stephen L.

Subjects
Azo compounds -- Chemical properties, Chemical bonds -- Analysis, Palladium catalysts -- Chemical properties, Biological sciences, Chemistry
Abstract

The development of a new method for the assembly of unsymmetrical carbazoles which involves the selective intramolecular functionalization of an arene C-H bond and the formation of a new arene C-N bond are reported.

Published
2008

3. Palladium-catalyzed carbonylation of aryl tosylates and mesylates

Author

Munday, Rachel H., Martinelli, Joseph R., and Buchwald, Stephen L.

Subjects
Carbonylation -- Analysis, Organosulfur compounds -- Chemical properties, Organosulfur compounds -- Thermal properties, Palladium catalysts -- Chemical properties, Chemistry
Abstract

A mild and general procedure is developed for the carbonylation of aryl tosylates and mesylates at atmospheric pressure of carbon monoxide and low temperatures. A commercially available, air stable dccp.2HB[F.sub.4] salt is used as the supporting ligand in this preparation.

Published
2008

4. Vinyldimethylphenylsilanes as safety catch silanols in fluoride-free palladium-catalyzed cross-coupling reactions

Author

Anderson, James C. and Munday, Rachel H.

Subjects
Palladium -- Chemical properties, Palladium -- Research, Silane -- Research, Biological sciences, Chemistry
Abstract

A series of five structurally diverse vinyldimethylphenylsilanes is shown to undergo a fluoride-free one-pot palladium-catalyzed cross-coupling reaction with phenyl iodide to give ipso coupled products in 62-86% yield. The limitations of the present model lie in the activation of Si-Ph versus protodesilylation by KOTMS/18-C-6, which seems sensitive to the sterics of cis substituents.

Published
2004

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