The three-component Mannich reaction between in situ generated imines and enolates gives rapid access to diverse beta- and gamma- amino carbonyl compounds. The employment of tailored catalysts and promoters permits control of regio-, chemo-, and stereoselectivity in both direct and indirect variants of the Mannich reaction
Luca Bernardi, Alfredo Ricci (2014). Third component enolizable carbonyl compound (Mannich reaction). Stuttgart : Georg Thieme Verlag.
Third component enolizable carbonyl compound (Mannich reaction)
BERNARDI, LUCA;
2014
Abstract
The three-component Mannich reaction between in situ generated imines and enolates gives rapid access to diverse beta- and gamma- amino carbonyl compounds. The employment of tailored catalysts and promoters permits control of regio-, chemo-, and stereoselectivity in both direct and indirect variants of the Mannich reactionFile in questo prodotto:
Eventuali allegati, non sono esposti
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
