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Allenylation and propargylation reactions of ketones, aldehydes, imines, and iminium ions using organoboronates and related derivatives

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posted on 2024-11-16, 02:39 authored by Thanaphat Thaima, Farzad Zamani, Christopher HylandChristopher Hyland, Stephen PyneStephen Pyne
Allenyl- and propargylboronates have emerged as versatile reagents to effect regioselective propargylation or allenylation reactions of aldehydes, ketones, imines, and iminium ions. These boron-­derived reagents have the ability to undergo transmetalation reactions with other metals (Ag, Cu, In, and Zn), often using only catalytic amounts of these metals, leading to more facile and highly regioselective reactions. Enantioselective organocatalyzed reactions have also been developed using, chiral diols, aminophenols, and phosphoric ­acids. This short review highlights recent developments in this area.

Funding

New strategies for the stereoselective synthesis of Stemona alkaloids and the discovery of new bioactive molecules

Australian Research Council

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History

Citation

Thaima, T., Zamani, F., Hyland, C. J. T. & Pyne, S. G. (2017). Allenylation and propargylation reactions of ketones, aldehydes, imines, and iminium ions using organoboronates and related derivatives. Synthesis (Germany), 49 (7), 1461-1480.

Journal title

Synthesis (Germany)

Volume

49

Issue

7

Pagination

1461-1480

Language

English

RIS ID

112064

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