Conformationally constrained bis(oxazoline) derived chiral catalyst: A highly effective enantioselective Diels-Alder reaction-Reference-Cited by-同舟云学术

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Conformationally constrained bis(oxazoline) derived chiral catalyst: A highly effective enantioselective Diels-Alder reaction

Published:1996-05 Issue:22 Volume:37 Page:3815-3818
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ghosh Arun K.,Mathivanan Packiarajan,Cappiello John

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference39 articles.

1. Cycloaddition Reactions in Organic Synthesis;Carruthers,1990

2. Cycloaddition Reactions in Carbohydrate Chemistry;Giuliano,1992

3. New enantioselective routes to biologically interesting compounds

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1. Reaction-Agnostic Featurization of Bidentate Ligands for Bayesian Ridge Regression of Enantioselectivity;ACS Catalysis;2024-06-04

2. Uniquely Enabling Mechanism for Bis-oxazoline Copper(II)-Catalyzed Azidation of Pyranosides and Furanosides;ACS Catalysis;2022-09-30

3. Quantitative Structure–Selectivity Relationships in Enantioselective Catalysis: Past, Present, and Future;Chemical Reviews;2019-12-30

4. Stereodivergent Catalysis;Chemical Reviews;2018-04-20

5. Metal-Controlled Switching of Enantioselectivity in the Mukaiyama–Michael Reaction of α,β-Unsaturated 2-Acyl Imidazoles Catalyzed by Chiral Metal–Pybox Complexes;The Journal of Organic Chemistry;2018-04-16

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