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2000
Volume 8, Issue 1
  • ISSN: 1570-193X
  • E-ISSN: 1875-6298

Abstract

This review will focus on the recent applications of chiral Schiff base in asymmetric catalysis. The developments in the preparation and use of chiral Schiff base in a variety of asymmetric transformations will be covered. Some remarkable characteristics and catalytic mechanisms of these reactions will be mentioned and the limitations of some asymmetric reactions will be also discussed.

© Bentham Science Publishers
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/content/journals/mroc/10.2174/157019311793979927
2011-02-01
2025-09-10

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  • Article Type:     Research Article
Keyword(s): Aldol Reaction; Aldol reaction, Strecker reaction; asymmetric catalysis; Asymmetric Strecker Reaction; asymmetric transformation; Baeyer-Villiger oxidation; Baeyer-Villiger Oxidation; BINOL; Boc-tert-leucine; Borohydride Reduction; Cu-Sm-Schiff base catalyst; Cubis complex; cyclopropanation; Cyclopropanation; diethylzinc; dinuclear dicyanide complex; EDA; enantioselectivity; Ene reaction; ethyl glyoxylate; Ethyl Mandelate; FABMS; HDA; Henry Reaction; hetero dienophile; Hetero-Diels-Alder reaction; Mannich reaction; mechanism; Ni2-Schiff base complex; NMR; NOBIN; NOESY; ROESY; Schiff base; Schiff base catalyst; SEGPHOS-Pd complex; single-wall carbon nanotube; Sulfoxidation; synthetic methods; tetrahydropyranones; TIBS; Tridentate Schiff base chromium complex; trimethylsilylcyanation; UHP; X-ray crystallography; Zn(salen) complex

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