Phosphine-catalyzed asymmetric additions of malonate esters to {gamma}-substituted allenoates and allenamides
Because carbonyl groups are ubiquitous in organic chemistry, the ability to synthesize functionalized carbonyl compounds, particularly enantioselectively, is an important objective. We have developed a straightforward and versatile method for catalytic asymmetric carbon-carbon bond formation at the...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2010-11, Vol.107 (48), p.20652-20654 |
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container_title | Proceedings of the National Academy of Sciences - PNAS |
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creator | Sinisi, Riccardo Sun, Jianwei Fu, Gregory C |
description | Because carbonyl groups are ubiquitous in organic chemistry, the ability to synthesize functionalized carbonyl compounds, particularly enantioselectively, is an important objective. We have developed a straightforward and versatile method for catalytic asymmetric carbon-carbon bond formation at the γ-position of carbonyl compounds, specifically, phosphine-catalyzed additions of malonate esters to γ-substituted allenoates and allenamides. Mechanistic studies have provided insight into the reaction pathway. |
doi_str_mv | 10.1073/pnas.1003597107 |
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subjects | Carbon Catalysis Catalysts Chemical bonds Organic chemistry |
title | Phosphine-catalyzed asymmetric additions of malonate esters to {gamma}-substituted allenoates and allenamides |
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