4.7 Article

Iodine-Catalyzed Double [4+2] Oxidative Annulations for the Synthesis of Bipyrazines from Ketones and Diamines by a Domino Strategy

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 364, Issue 2, Pages 355-361

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.202100991

Keywords

Double annulation; bipyrazine; domino reaction; iodine; [4+2] cyclization

Funding

  1. Leading Innovative and Entrepreneur Team Introduction Program of Zhejiang [2019R01005]

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An iodine-catalyzed double [4+2] oxidative annulation of ketones and diamines is reported, leading to the synthesis of substituted dimeric pyrazines under metal-free conditions through a multi-pathway coupled domino strategy. During this process, one C-C and four C-N bonds are formed from two ketones and two diamines.
An iodine-catalyzed double [4+2] oxidative annulation of ketones and diamines is described. A multi-pathway coupled domino strategy has been developed for the synthesis of substituted dimeric pyrazines under metal-free conditions. One C-C and four C-N bonds are formed during this double [4+2] oxidative annulation process from two ketones and two diamines.

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