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Polyborylated reagents for modern organic synthesis
Diverse kinds of gem- and vic-diborylated compounds are now readily available thanks to advances in gem-diborylation of lithium carbenoids as well as vic-diborylation of carbon–carbon multiple bonds with diboron compounds. These diborylated reagents lead to invention of polyborylated reagents and ma...
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Formato: | Texto |
Lenguaje: | English |
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The Japan Academy
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805506/ https://www.ncbi.nlm.nih.gov/pubmed/18941288 http://dx.doi.org/10.2183/pjab.84.75 |
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author | SHIMIZU, Masaki HIYAMA, Tamejiro |
author_facet | SHIMIZU, Masaki HIYAMA, Tamejiro |
author_sort | SHIMIZU, Masaki |
collection | PubMed |
description | Diverse kinds of gem- and vic-diborylated compounds are now readily available thanks to advances in gem-diborylation of lithium carbenoids as well as vic-diborylation of carbon–carbon multiple bonds with diboron compounds. These diborylated reagents lead to invention of polyborylated reagents and many novel and useful synthetic methods for supreme stereocontrol. This review summarizes preparative methods and synthetic reactions of di- and polyborylated reagents with the emphasis on multiple bond formation. |
format | Text |
id | pubmed-2805506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | The Japan Academy |
record_format | MEDLINE/PubMed |
spelling | pubmed-28055062012-06-19 Polyborylated reagents for modern organic synthesis SHIMIZU, Masaki HIYAMA, Tamejiro Proc Jpn Acad Ser B Phys Biol Sci Review Diverse kinds of gem- and vic-diborylated compounds are now readily available thanks to advances in gem-diborylation of lithium carbenoids as well as vic-diborylation of carbon–carbon multiple bonds with diboron compounds. These diborylated reagents lead to invention of polyborylated reagents and many novel and useful synthetic methods for supreme stereocontrol. This review summarizes preparative methods and synthetic reactions of di- and polyborylated reagents with the emphasis on multiple bond formation. The Japan Academy 2008-03 2008-03-12 /pmc/articles/PMC2805506/ /pubmed/18941288 http://dx.doi.org/10.2183/pjab.84.75 Text en © 2008 The Japan Academy This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review SHIMIZU, Masaki HIYAMA, Tamejiro Polyborylated reagents for modern organic synthesis |
title | Polyborylated reagents for modern organic synthesis |
title_full | Polyborylated reagents for modern organic synthesis |
title_fullStr | Polyborylated reagents for modern organic synthesis |
title_full_unstemmed | Polyborylated reagents for modern organic synthesis |
title_short | Polyborylated reagents for modern organic synthesis |
title_sort | polyborylated reagents for modern organic synthesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805506/ https://www.ncbi.nlm.nih.gov/pubmed/18941288 http://dx.doi.org/10.2183/pjab.84.75 |
work_keys_str_mv | AT shimizumasaki polyborylatedreagentsformodernorganicsynthesis AT hiyamatamejiro polyborylatedreagentsformodernorganicsynthesis |