Jump to main content
Jump to site search

Issue 59, 2016, Issue in Progress
Previous Article Next Article

In situ generation of dihydropyridine for the enantioselective transfer hydrogenation of 1,4-benzoxazines

Author affiliations

Abstract

A new strategy for the enantioselective transfer hydrogenation of benzoxazines involving an in situ generation of Hantzsch ester has been developed. Dihydroadducts were isolated in good yields (75–99%) and enantioselectivities (89–96% ee).

Graphical abstract: In situ generation of dihydropyridine for the enantioselective transfer hydrogenation of 1,4-benzoxazines

Back to tab navigation

Supplementary files

Publication details

The article was received on 24 Feb 2016, accepted on 25 May 2016 and first published on 27 May 2016


Article type: Communication
DOI: 10.1039/C6RA04930C
Citation: RSC Adv., 2016,6, 54185-54188
  •   Request permissions

    In situ generation of dihydropyridine for the enantioselective transfer hydrogenation of 1,4-benzoxazines

    A. Aillerie, C. Gosset, C. Dumont, V. Skrzypczak, P. Champetter, S. Pellegrini, T. Bousquet and L. Pélinski, RSC Adv., 2016, 6, 54185
    DOI: 10.1039/C6RA04930C

Search articles by author

Spotlight

Advertisements