cis,cis-Spiro[4.4]nonane-1,6-diol: A new chiral auxiliary for the asymmetric Diels-Alder reaction-Reference-Cited by-同舟云学术

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cis,cis-Spiro[4.4]nonane-1,6-diol: A new chiral auxiliary for the asymmetric Diels-Alder reaction

Published:1996-12 Issue:12 Volume:7 Page:3521-3526
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Nieman James A.,Keay Brian A.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference19 articles.

1. Lewis Acids and Selectivity in Organic Synthesis;Santelli,1996

2. The chiral pool as a source of enantioselective catalysts and auxiliaries

3. Catalytic asymmetric Diels Alder reactions

4. Acceleration and selectivity enhancement of Diels-Alder reactions by special and catalytic methods

5. Comprehensive Organic Synthesis: Selectivity, Strategy and Efficiency in Modern Organic Chemistry;Oppolzer,1991

Cited by 23 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Asymmetric intramolecular Friedel–Crafts reaction catalyzed by a spiropyrrolidine organocatalyst: Enantioselective construction of indolizine and azepine frameworks;Tetrahedron Letters;2018-11

2. Spiro Ligands for Asymmetric Catalysis;Ligand Design in Metal Chemistry;2016-09-02

3. Cycloadditions II;Key Chiral Auxiliary Applications;2014

4. Chiral Spiro Ligands;Privileged Chiral Ligands and Catalysts;2011-04-07

5. ChemInform Abstract: cis,cis-Spiro(4.4)nonane-1,6-diol: A New Chiral Auxiliary for the Asymmetric Diels-Alder Reaction.;ChemInform;2010-08-04

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