Novel non-azacyclo 1,2-aminoalcohols derived from l-Phe and highly enantioselective addition of diethylzinc to aryl aldehydes
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Process Chemistry and Technology,Catalysis
Reference34 articles.
1. Catalytic Asymmetric Organozinc Additions to Carbonyl Compounds
2. Enantioselective Addition of Organometallic Reagents to Carbonyl Compounds: Chirality Transfer, Multiplication, and Amplification
3. Enantioselective addition of organozinc reagents to aldehydes
4. Stereoselective Organic Reactions: Catalysts for Carbonyl Addition Processes
5. Chiral bis(amino alcohol)oxalamides as ligands for asymmetric catalysis. Ti(IV) catalyzed enantioselective addition of diethylzinc to aldehydes
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1. Asymmetric epoxidation of enones using cumyl hydroperoxide and in situ generated zinc complexes of chiral pyrrolidinyl alcohols;Tetrahedron: Asymmetry;2017-11
2. The synthesis of chiral amino diol tridentate ligands and their enantioselective induction during the addition of diethylzinc to aldehydes;Tetrahedron: Asymmetry;2014-02
3. The first catalytic asymmetric addition of diethylzinc to aldehyde promoted by chiral thiourea;Chinese Chemical Letters;2011-11
4. Synthesis of sterically constrained tricyclic pyrrolidinyl alcohol ligands for the enantioselective ethylation of aryl aldehydes: assessment of the influence of ring strain and N-alkyl chain length on asymmetric induction;Tetrahedron: Asymmetry;2011-02
5. Establishment of the absolute configuration of the bioactive marine alkaloid eudistomin X by stereospecific synthesis;Tetrahedron Letters;2011-02
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