Boron enolates derived from alpha-heterosubstituted thioacetates and bearing menthone-derived chiral ligands react with aldehydes to give anti aldols with excellent diastero- and enantiocontrol.

A HIGHLY ENANTIOSELECTIVE AND DIASTEREOSELECTIVE ALDOL REACTION FOR ALPHA-HETEROSUBSTITUTED THIOACETATES / C.M.A. GENNARI, A. VULPETTI, D. MORESCA. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 35:27(1994), pp. 4857-4860.

A HIGHLY ENANTIOSELECTIVE AND DIASTEREOSELECTIVE ALDOL REACTION FOR ALPHA-HETEROSUBSTITUTED THIOACETATES

C.M.A. GENNARI
Primo
;
1994

Abstract

Boron enolates derived from alpha-heterosubstituted thioacetates and bearing menthone-derived chiral ligands react with aldehydes to give anti aldols with excellent diastero- and enantiocontrol.
Settore CHIM/06 - Chimica Organica
Article (author)
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

Caricamento pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/177057
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 13
  • ???jsp.display-item.citation.isi??? 16
social impact