Tandem ring-closing metathesis/isomerization reactions for the total synthesis of violacein

A series of 5-substituted 2-pyrrolidinones was synthesized through a one-pot ruthenium alkylidene-catalyzed tandem RCM/isomerization/nucleophilic addition sequence. The intermediates resulting from RCM/isomerization showed reactivity toward electrophiles in aldol condensation reactions which provide...

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Main Authors: Petersen, Mette T., Nielsen, Thomas E.
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2013
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Online Access:https://hdl.handle.net/10356/99817
http://hdl.handle.net/10220/17769
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-998172020-03-07T12:47:10Z Tandem ring-closing metathesis/isomerization reactions for the total synthesis of violacein Petersen, Mette T. Nielsen, Thomas E. School of Biological Sciences DRNTU::Science::Biological sciences A series of 5-substituted 2-pyrrolidinones was synthesized through a one-pot ruthenium alkylidene-catalyzed tandem RCM/isomerization/nucleophilic addition sequence. The intermediates resulting from RCM/isomerization showed reactivity toward electrophiles in aldol condensation reactions which provided a new entry for the total synthesis of the antileukemic natural product violacein. 2013-11-19T04:00:21Z 2019-12-06T20:11:56Z 2013-11-19T04:00:21Z 2019-12-06T20:11:56Z 2013 2013 Journal Article Petersen, M. T., & Nielsen, T. E. (2013). Tandem Ring-Closing Metathesis/Isomerization Reactions for the Total Synthesis of Violacein. Organic Letters, 15(8), 1986-1989. https://hdl.handle.net/10356/99817 http://hdl.handle.net/10220/17769 10.1021/ol400654r en Organic letters
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic DRNTU::Science::Biological sciences
spellingShingle DRNTU::Science::Biological sciences
Petersen, Mette T.
Nielsen, Thomas E.
Tandem ring-closing metathesis/isomerization reactions for the total synthesis of violacein
description A series of 5-substituted 2-pyrrolidinones was synthesized through a one-pot ruthenium alkylidene-catalyzed tandem RCM/isomerization/nucleophilic addition sequence. The intermediates resulting from RCM/isomerization showed reactivity toward electrophiles in aldol condensation reactions which provided a new entry for the total synthesis of the antileukemic natural product violacein.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Petersen, Mette T.
Nielsen, Thomas E.
format Article
author Petersen, Mette T.
Nielsen, Thomas E.
author_sort Petersen, Mette T.
title Tandem ring-closing metathesis/isomerization reactions for the total synthesis of violacein
title_short Tandem ring-closing metathesis/isomerization reactions for the total synthesis of violacein
title_full Tandem ring-closing metathesis/isomerization reactions for the total synthesis of violacein
title_fullStr Tandem ring-closing metathesis/isomerization reactions for the total synthesis of violacein
title_full_unstemmed Tandem ring-closing metathesis/isomerization reactions for the total synthesis of violacein
title_sort tandem ring-closing metathesis/isomerization reactions for the total synthesis of violacein
publishDate 2013
url https://hdl.handle.net/10356/99817
http://hdl.handle.net/10220/17769
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