Efficient synthesis of β-amino alcohols by regioselective ring-opening of epoxides with anilines catalyzed by sulfated zirconia under solvent-free conditions-Reference-Cited by-同舟云学术

Efficient synthesis of β-amino alcohols by regioselective ring-opening of epoxides with anilines catalyzed by sulfated zirconia under solvent-free conditions

Published:2008-03 Issue:5 Volume:9 Page:950-954
ISSN:1566-7367
Container-title:Catalysis Communications
language:en
Short-container-title:Catalysis Communications

Author:

Reddy Benjaram M.,Patil Meghshyam K.,Reddy Baddam T.,Park Sang-Eon

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,General Chemistry,Catalysis

Reference35 articles.

1. re- andsi-Face-Selective Nitroaldol Reactions Catalyzed by a Rigid Chiral Quaternary Ammonium Salt: A Highly Stereoselective Synthesis of the HIV Protease Inhibitor Amprenavir (Vertex 478)

2. Zr-Catalyzed Kinetic Resolution of Allylic Ethers and Mo-Catalyzed Chromene Formation in Synthesis. Enantioselective Total Synthesis of the Antihypertensive Agent (S,R,R,R)-Nebivolol

3. 1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis

4. 1,2,3-oxathiazolidines. Heterocyclic system

5. Regioalternating selectivity in the metal salt catalyzed aminolysis of styrene oxide

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