Synthesis of β-amino alcohols by ring opening of epoxides with amines catalyzed by sulfated tin oxide under mild and solvent-free conditions
One significant and elegant method for creating β-amino alcohols, which are useful intermediates for the synthesis of many different natural and synthetic pharmaceutical compounds, is to open the rings of epoxides with amines. When sulfated tin oxide catalyst (2 mol%) is present, epoxides c...
Main Authors: | Chintalapudi Rama Krishna, K. Aparna Seetharam, T. N. V. S. S. Satyadev |
---|---|
Format: | Article |
Language: | English |
Published: |
Growing Science
2024-01-01
|
Series: | Current Chemistry Letters |
Online Access: | http://www.growingscience.com/ccl/Vol13/ccl_2023_74.pdf |
Similar Items
-
Rapid and Efficient N-tert-butoxy carbonylation of Amines Catalyzed by Sulfated Tin Oxide Under Solvent-free Condition
by: J. K. Prashanth Kumar, et al.
Published: (2018-12-01) -
Ring-Opening of Epoxides with Amines for Synthesis of β-Amino Alcohols in a Continuous-Flow Biocatalysis System
by: Li-Hua Du, et al.
Published: (2020-12-01) -
Asymmetric Ring-Opening of Epoxides Catalyzed by Metal–Salen Complexes
by: Anna Lidskog, et al.
Published: (2020-06-01) -
Synthesis of Azanucleosides through Regioselective Ring-Opening of Epoxides Catalyzed by Sulphated Zirconia under Microwave and Solvent-Free Conditions
by: Guillermo E. Negrón-Silva, et al.
Published: (2012-03-01) -
Copolymerization of Phthalic Anhydride with Epoxides Catalyzed by Amine-Bis(Phenolate) Chromium(III) Complexes
by: Wiktor Bukowski, et al.
Published: (2021-05-01)