4.7 Article

Multifunctional Click Prolinamides: A New Platform for Asymmetric Aldol Reactions in the Presence of Water with Catalyst Recycling

期刊

ADVANCED SYNTHESIS & CATALYSIS
卷 355, 期 2-3, 页码 274-280

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201200856

关键词

asymmetric catalysis; click chemistry; diastereoselectivity; green chemistry; organocatalysis; recycling organocatalyst

资金

  1. Department of Science and Technology (DST)
  2. Department of Biotechnology (DBT)
  3. Council of Science and Industrial Research (CSIR)
  4. CSIR India

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Click chemistry is combined with organocatalysis to fabricate a multifunctional C3-symmetrical dendritic prolinamide with a hydrophobic aromatic core and hydrophilic triazolinium arms that exhibit high efficiency in catalyzing the asymmetric aldol reaction with cyclic ketones. The catalyst is water-compatible and remains active for five consecutive catalytic runs with a low catalyst loading (2mol%), yielding the aldol products in high yields, diastereo- and enantioselectivities.

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