Application of (2R,3R)-dihydroxy-1,2,3,4-tetrahydronaphthalene to asymmetric synthesis
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference12 articles.
1. Cyclic chiral diols with C2 symmetry: Synthesis of (2R,3R)-dihydroxy-1,2,3,4-tetrahydronaphthalene
2. OPTICAL ACTIVITY AND CHEMICAL STRUCTURE*
3. Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters
4. Asymmetric conjugate addition of organometallic reagents to chiral α, β-unsaturated esters
5. Regio-, stereo-, and enantioselectivity in the electrophilic reactions of 2-amino-4-phenyl-3-butenenitriles
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1. Alkylation and Related Reactions II;Key Chiral Auxiliary Applications;2014
2. Asymmetric Synthesis of Functionalized Tetrahydronaphthalenesviaan Organocatalytic Nitroalkane-Michael/Henry Domino Reaction;Advanced Synthesis & Catalysis;2013-04-08
3. ChemInform Abstract: Application of (2R,3R)-Dihydroxy-1,2,3,4-tetrahydronaphthalene to Asymmetric Synthesis.;ChemInform;2010-08-03
4. Functions Bearing Two Oxygens, R12C(OR2)2;Comprehensive Organic Functional Group Transformations II;2005
5. Chemoenzymatic synthesis of conduritol analogues;Tetrahedron Letters;2004-12
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