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Cyclopropene-templated assembly of medium cycles via ru-catalyzed ring-closing metathesis

An expeditious click-click cyclize strategy for the assembly of medium-sized heterocyclic rings is described. The sequence involves the reaction of cycloprop-2-ene carboxylic acids with unsaturated amines to furnish amides, which are further subjected to a Cu-catalyzed directed carbomagnesiation and...

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Egile Nagusiak: Rubin, M. A., Рубин, М. А.
Formatua: Статья
Hizkuntza:English
Argitaratua: American Chemical Society 2020
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Sarrera elektronikoa:https://dspace.ncfu.ru/handle/20.500.12258/12117
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id ir-20.500.12258-12117
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spelling ir-20.500.12258-121172020-07-29T09:32:20Z Cyclopropene-templated assembly of medium cycles via ru-catalyzed ring-closing metathesis Rubin, M. A. Рубин, М. А. Cycloaddition Reaction Cyclopropenes Vinylcarbene An expeditious click-click cyclize strategy for the assembly of medium-sized heterocyclic rings is described. The sequence involves the reaction of cycloprop-2-ene carboxylic acids with unsaturated amines to furnish amides, which are further subjected to a Cu-catalyzed directed carbomagnesiation and a ring-closing olefin metathesis reaction. This methodology allows for the efficient preparation of lactams with ring sizes up to 10 2020-06-25T13:11:19Z 2020-06-25T13:11:19Z 2020 Статья Yamanushkin, P., Smith, S.P., Petillo, P.A., Rubin, M. Cyclopropene-Templated Assembly of Medium Cycles via Ru-Catalyzed Ring-Closing Metathesis // Organic Letters. - 2020. - Volume 22. - Issue 9. - Pages 3542-3546 http://hdl.handle.net/20.500.12258/12117 en Organic Letters application/pdf application/pdf American Chemical Society
institution СКФУ
collection Репозиторий
language English
topic Cycloaddition Reaction
Cyclopropenes
Vinylcarbene
spellingShingle Cycloaddition Reaction
Cyclopropenes
Vinylcarbene
Rubin, M. A.
Рубин, М. А.
Cyclopropene-templated assembly of medium cycles via ru-catalyzed ring-closing metathesis
description An expeditious click-click cyclize strategy for the assembly of medium-sized heterocyclic rings is described. The sequence involves the reaction of cycloprop-2-ene carboxylic acids with unsaturated amines to furnish amides, which are further subjected to a Cu-catalyzed directed carbomagnesiation and a ring-closing olefin metathesis reaction. This methodology allows for the efficient preparation of lactams with ring sizes up to 10
format Статья
author Rubin, M. A.
Рубин, М. А.
author_facet Rubin, M. A.
Рубин, М. А.
author_sort Rubin, M. A.
title Cyclopropene-templated assembly of medium cycles via ru-catalyzed ring-closing metathesis
title_short Cyclopropene-templated assembly of medium cycles via ru-catalyzed ring-closing metathesis
title_full Cyclopropene-templated assembly of medium cycles via ru-catalyzed ring-closing metathesis
title_fullStr Cyclopropene-templated assembly of medium cycles via ru-catalyzed ring-closing metathesis
title_full_unstemmed Cyclopropene-templated assembly of medium cycles via ru-catalyzed ring-closing metathesis
title_sort cyclopropene-templated assembly of medium cycles via ru-catalyzed ring-closing metathesis
publisher American Chemical Society
publishDate 2020
url https://dspace.ncfu.ru/handle/20.500.12258/12117
work_keys_str_mv AT rubinma cyclopropenetemplatedassemblyofmediumcyclesviarucatalyzedringclosingmetathesis
AT rubinma cyclopropenetemplatedassemblyofmediumcyclesviarucatalyzedringclosingmetathesis
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