Unknown

Dataset Information

0

Catalytic enantioselective hetero-Diels-Alder reactions of an azo compound.


ABSTRACT: This communication describes studies in which an azo hetero-Diels-Alder adduct was furnished in high regio- and enantioselectivity using azopyridine as a reagent and silver as a catalyst. The obtained hetero-Diels-Alder adduct was easily converted to the corresponding chiral 1,4-diamino alcohol.

SUBMITTER: Kawasaki M 

PROVIDER: S-EPMC2546566 | biostudies-literature | 2006 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Catalytic enantioselective hetero-Diels-Alder reactions of an azo compound.

Kawasaki Masanori M   Yamamoto Hisashi H  

Journal of the American Chemical Society 20061201 51


This communication describes studies in which an azo hetero-Diels-Alder adduct was furnished in high regio- and enantioselectivity using azopyridine as a reagent and silver as a catalyst. The obtained hetero-Diels-Alder adduct was easily converted to the corresponding chiral 1,4-diamino alcohol. ...[more]

Similar Datasets

| S-EPMC4464410 | biostudies-literature
| S-EPMC8251941 | biostudies-literature
| S-EPMC2918383 | biostudies-literature
| S-EPMC7508818 | biostudies-literature
| S-EPMC7589293 | biostudies-literature
| S-EPMC8152632 | biostudies-literature
| S-EPMC3458765 | biostudies-other
| S-EPMC6541354 | biostudies-literature
| S-EPMC2631179 | biostudies-literature
| S-EPMC3170844 | biostudies-literature