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Diastereo- and enantioselective copper catalyzed hydroallylation of disubstituted cyclopropenes
A highly diastereo- and enantioselective protocol for the hydroallylation of 1,1- and 1,2-disubstituted cyclopropenes has been developed utilizing an in situ formed copper hydride. A variety of allyl electrophiles could be utilized yielding a diverse range of trisubstituted cyclopropanes. Finally a...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6115688/ https://www.ncbi.nlm.nih.gov/pubmed/30310580 http://dx.doi.org/10.1039/c8sc02085j |
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author | Sommer, Heiko Marek, Ilan |
author_facet | Sommer, Heiko Marek, Ilan |
author_sort | Sommer, Heiko |
collection | PubMed |
description | A highly diastereo- and enantioselective protocol for the hydroallylation of 1,1- and 1,2-disubstituted cyclopropenes has been developed utilizing an in situ formed copper hydride. A variety of allyl electrophiles could be utilized yielding a diverse range of trisubstituted cyclopropanes. Finally a preliminary enantioselective variant could be established employing a recently described P-stereogenic xantphos derivative as ligand. |
format | Online Article Text |
id | pubmed-6115688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-61156882018-10-11 Diastereo- and enantioselective copper catalyzed hydroallylation of disubstituted cyclopropenes Sommer, Heiko Marek, Ilan Chem Sci Chemistry A highly diastereo- and enantioselective protocol for the hydroallylation of 1,1- and 1,2-disubstituted cyclopropenes has been developed utilizing an in situ formed copper hydride. A variety of allyl electrophiles could be utilized yielding a diverse range of trisubstituted cyclopropanes. Finally a preliminary enantioselective variant could be established employing a recently described P-stereogenic xantphos derivative as ligand. Royal Society of Chemistry 2018-07-02 /pmc/articles/PMC6115688/ /pubmed/30310580 http://dx.doi.org/10.1039/c8sc02085j Text en This journal is © The Royal Society of Chemistry 2018 https://creativecommons.org/licenses/by-nc/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Sommer, Heiko Marek, Ilan Diastereo- and enantioselective copper catalyzed hydroallylation of disubstituted cyclopropenes |
title | Diastereo- and enantioselective copper catalyzed hydroallylation of disubstituted cyclopropenes
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title_full | Diastereo- and enantioselective copper catalyzed hydroallylation of disubstituted cyclopropenes
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title_fullStr | Diastereo- and enantioselective copper catalyzed hydroallylation of disubstituted cyclopropenes
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title_full_unstemmed | Diastereo- and enantioselective copper catalyzed hydroallylation of disubstituted cyclopropenes
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title_short | Diastereo- and enantioselective copper catalyzed hydroallylation of disubstituted cyclopropenes
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title_sort | diastereo- and enantioselective copper catalyzed hydroallylation of disubstituted cyclopropenes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6115688/ https://www.ncbi.nlm.nih.gov/pubmed/30310580 http://dx.doi.org/10.1039/c8sc02085j |
work_keys_str_mv | AT sommerheiko diastereoandenantioselectivecoppercatalyzedhydroallylationofdisubstitutedcyclopropenes AT marekilan diastereoandenantioselectivecoppercatalyzedhydroallylationofdisubstitutedcyclopropenes |