1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis

1996 ◽  
Vol 96 (2) ◽  
pp. 835-876 ◽  
Author(s):  
David J. Ager ◽  
Indra Prakash ◽  
David R. Schaad
Keyword(s):  
Asymmetric Synthesis ◽  
Amino Alcohols ◽  
Chiral Auxiliaries ◽  
Heterocyclic Derivatives

Chiral β-Amino Alcohols and Derivatives in the Asymmetric Synthesis of Tetrahydroisoquinolines

ChemInform ◽  
2004 ◽  
Vol 35 (31) ◽  
Author(s):  
Eneritz Anakabe ◽  
Dolores Badia ◽  
Luisa Carrillo ◽  
Efraim Reyes ◽  
Jose L. Vicario
Keyword(s):  
Asymmetric Synthesis ◽  
Amino Alcohols

scholarly journals Cellulose recycling as a source of raw chirality

2013 ◽  
Vol 85 (8) ◽  
pp. 1683-1692 ◽  
Author(s):  
Valeria Corne ◽  
María Celeste Botta ◽  
Enrique D. V. Giordano ◽  
Germán F. Giri ◽  
David F. Llompart ◽  
...  
Keyword(s):  
Organic Chemistry ◽  
Organic Carbon ◽  
Asymmetric Synthesis ◽  
Building Blocks ◽  
Biologically Active ◽  
Raw Material ◽  
Chiral Auxiliaries ◽  
High Chemical ◽  
Chiral Structure

Modern organic chemistry requires easily obtainable chiral building blocks that show high chemical versatility for their application in the synthesis of enantiopure compounds. Biomass has been demonstrated to be a widely available raw material that represents the only abundant source of renewable organic carbon. Through the pyrolitic conversion of cellulose or cellulose-containing materials it is possible to produce levoglucosenone, a highly functionalized chiral structure. This compound has been innovatively used as a template for the synthesis of key intermediates of biologically active products and for the preparation of chiral auxiliaries, catalysts, and organocatalysts for their application in asymmetric synthesis.

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