A novel, highly stereoselective route for pharmaceutically relevant octahydroindole-2-carboxylates bearing a quaternary stereocenter has been developed. The key chiral intermediates 3 have been prepared in good yields and enantiomeric excesses up to 98%. A broad substrate range has been tolerated under the reaction conditions.

Stereoselective Michael additions on α-​aminoacrylates as the key step to an L-​Oic analogue bearing a quaternary stereocenter / F.M. Cecchinelli, G. Celentano, A. Puglisi, N. Gaggero. - In: ORGANIC & BIOMOLECULAR CHEMISTRY. - ISSN 1477-0520. - 18:4(2020 Jan 28), pp. 671-674. [10.1039/c9ob02084e]

Stereoselective Michael additions on α-​aminoacrylates as the key step to an L-​Oic analogue bearing a quaternary stereocenter

G. Celentano
Secondo
;
A. Puglisi
Penultimo
;
N. Gaggero
Ultimo
2020

Abstract

A novel, highly stereoselective route for pharmaceutically relevant octahydroindole-2-carboxylates bearing a quaternary stereocenter has been developed. The key chiral intermediates 3 have been prepared in good yields and enantiomeric excesses up to 98%. A broad substrate range has been tolerated under the reaction conditions.
Settore CHIM/06 - Chimica Organica
28-gen-2020
dic-2019
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/701080
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