Highly stereoselective and stereospecific syntheses of a variety of quercitols from d-(−)-quinic acid
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference32 articles.
1. Synthesis of Two New Quercitol (Deoxyinositol) Stereoisomers. Nuclear Magnetic Resonance and Optical Rotatory Configurational Proofs1,2
2. A Convenient Synthesis of (±)-talo-Quercitol (1-Deoxy-neo-Inositol) and (±)-vibo-Quercitol (1-Deoxy-myo-Inositol) via Ene Reaction of Singlet Oxygen
3. Cyclitols and their Derivatives;Hudlicky,1993
4. A Stereocontrolled Synthesis of proto-Quercitol
5. An Efficient and Stereospecific Synthesis of proto-Quercitol
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1. Antioxidant norbergenin derivatives from the leaves of Diospyros gilletii De Wild (Ebenaceae);Phytochemistry Letters;2020-04
2. Synthesis and biological activities of d - chiro -inositol analogues with insulin-like actions;European Journal of Medicinal Chemistry;2016-10
3. A novel stereoselective synthesis of (−)-quinic acid starting from the naturally abundant (−)-shikimic acid;Tetrahedron: Asymmetry;2015-12
4. Total Synthesis of Quercitols: (+)-allo-, (–)-proto-, (+)-talo-, (–)-gala-, (+)-gala-, neo-, and (–)-epi-Quercitol;Synlett;2014-12-17
5. Regioselective fluorination in synthesis of deoxyfluoro quercitols from d-(−)-quinic acid;Tetrahedron;2014-12
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