Unknown

Dataset Information

0

Enantioselective N-heterocyclic carbene catalyzed annulation reactions with imidazolidinones.


ABSTRACT: Add acetic acid: A highly stereoselective N-heterocyclic carbene (NHC)-catalyzed formal [4+2] annulation between ?,?-unsaturated aldehydes and imidazolidinones for the synthesis of imidazoles has been developed. Acetic acid serves as a key additive to achieve high chemoselectivity for the formal [4+2]?annulation product.

SUBMITTER: McCusker EO 

PROVIDER: S-EPMC3905989 | biostudies-literature | 2013 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Enantioselective N-heterocyclic carbene catalyzed annulation reactions with imidazolidinones.

McCusker Elizabeth O'Bryan EO   Scheidt Karl A KA  

Angewandte Chemie (International ed. in English) 20131118 51


Add acetic acid: A highly stereoselective N-heterocyclic carbene (NHC)-catalyzed formal [4+2] annulation between α,β-unsaturated aldehydes and imidazolidinones for the synthesis of imidazoles has been developed. Acetic acid serves as a key additive to achieve high chemoselectivity for the formal [4+2] annulation product. ...[more]

Similar Datasets

| S-EPMC2836487 | biostudies-literature
| S-EPMC4702349 | biostudies-literature
| S-EPMC11348421 | biostudies-literature
| S-EPMC5807440 | biostudies-literature
| S-EPMC6385844 | biostudies-other
| S-EPMC4702348 | biostudies-literature
| S-EPMC2996418 | biostudies-other
| S-EPMC2863089 | biostudies-literature
| S-EPMC5627355 | biostudies-literature
| S-EPMC5496987 | biostudies-literature