Allenes in Catalytic Asymmetric Synthesis and Natural Product Syntheses
Аллены в каталитическом асимметричном синтезе и синтезе природных соединений
2012-01-23
SCID: 54.1/7akucfx7
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allenescatalytic asymmetric synthesiscycloadditionnatural product synthesispropargylation
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Abstract (AI)
Allenes are the simplest class of cumulenes, with two contiguous C=C bonds, and show unique physical and chemical properties. These features make allenes particularly attractive in modern organic chemistry. In this Review, attention is paid to the advances made in catalytic asymmetric synthesis and natural product syntheses based on well-established reactions of allenes, such as propargylation, addition, cycloaddition, cycloisomerization, cyclization, etc., with or without catalysts. Their versatile reactivity, substituent-loading ability, axial to center chirality transfer, and controllable selectivity allow access to target molecules by unique and efficient approaches. The main topics in this Review are presented with selected examples from 2003 to 2011.
Key Findings
1
Allenes provide versatile reactivity, high substituent-loading ability, and axial-to-central chirality transfer, enabling access to target molecules via unique and efficient approaches.
2
Allenes, as the simplest cumulenes with contiguous C=C bonds, possess unique physical and chemical properties that make them attractive in organic chemistry.
3
The Review surveys selected advances and examples in these allene-based methods from 2003 to 2011, highlighting controllable selectivity in syntheses.
4
Well-established reactions of allenes (propargylation, addition, cycloaddition, cycloisomerization, cyclization) enable catalytic asymmetric synthesis and natural product syntheses, with or without catalysts.
Research Object
Allenes (cumulenes with two contiguous C=C bonds) used in catalytic asymmetric synthesis and natural product syntheses
Research Subject
Roles, reactions, and reactivity features of allenes enabling catalytic asymmetric transformations and applications in natural product synthesis, including propargylation, additions, cycloadditions, cycloisomerizations, cyclizations, chirality transfer, substituent loading, and controllable selectivity
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2012-01-23
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