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A novel hydrazide type organocatalyst for enantioselective Diels–Alder reactions†
Ichiro Suzuki,Masafumi Ando,Rumiko Shimabara,Ai Hirata,Kei Takeda
Organic & Biomolecular Chemistry Pub Date : 02/02/2011 00:00:00 , DOI:10.1039/C0OB01138J
Abstract

The development of a new class of hydrazide type organocatalyst, (4R,5R)-1,3-bis(isopropylamino)-4,5-dihenylimidazolidin-2-one 2a, for enantioselective Diels–Alder reactions between cyclopentadiene and α,β-unsaturated aldehydes are presented. The new organocatalyst 2a promoted the reaction, affording Diels–Alder adducts in good yields with good levels of enantioselectivity.

Graphical abstract: A novel hydrazide type organocatalyst for enantioselective Diels–Alder reactions
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