Enantioselective Cycloaddition Reactions Catalyzed by BINOL-Derived Phosphoric Acids and N-Triflyl Phosphoramides: Recent Advances

Journal article
(Review article)


Publication Details

Author(s): Held F, Grau D, Tsogoeva S
Journal: Molecules
Publisher: MDPI
Publication year: 2015
Volume: 20
Pages range: 16103-16126
ISSN: 1420-3049


Abstract


Over the last several years there has been a huge increase in the development and applications of new efficient organocatalysts for enantioselective pericyclic reactions, which represent one of the most powerful types of organic transformations. Among these processes are cycloaddition reactions (e.g., [3+2]; formal [3+3]; [4+2]; vinylogous [4+2] and 1,3-dipolar cycloadditions), which belong to the most utilized reactions in organic synthesis of complex nitrogen- and oxygen-containing heterocyclic molecules. This review presents the breakthrough realized in this field using chiral BINOL-derived phosphoric acids and N-triflyl phosphoramide organocatalysts.



FAU Authors / FAU Editors

Grau, Dominik
Lehrstuhl für Organische Chemie I
Held, Felix
Lehrstuhl für Organische Chemie I
Tsogoeva, Svetlana Prof. Dr.
Professur für Organische Chemie


How to cite

APA:
Held, F., Grau, D., & Tsogoeva, S. (2015). Enantioselective Cycloaddition Reactions Catalyzed by BINOL-Derived Phosphoric Acids and N-Triflyl Phosphoramides: Recent Advances. Molecules, 20, 16103-16126. https://dx.doi.org/10.3390/molecules200916103

MLA:
Held, Felix, Dominik Grau, and Svetlana Tsogoeva. "Enantioselective Cycloaddition Reactions Catalyzed by BINOL-Derived Phosphoric Acids and N-Triflyl Phosphoramides: Recent Advances." Molecules 20 (2015): 16103-16126.

BibTeX: 

Last updated on 2018-06-08 at 11:19