Cellulose recycling as a source of raw chirality

Author:

Corne Valeria1,Botta María Celeste1,Giordano Enrique D. V.1,Giri Germán F.1,Llompart David F.1,Biava Hernán D.1,Sarotti Ariel M.1,Mangione María I.1,Mata Ernesto G.1,Suárez Alejandra G.1,Spanevello Rolando A.1

Affiliation:

1. 1Instituto de Química Rosario, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario – CONICET, Suipacha 531, S2002LRK, Rosario, Argentina

Abstract

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.

Publisher

Walter de Gruyter GmbH

Subject

General Chemical Engineering,General Chemistry

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