The synthesis of enantiomerically enriched homoallylic alcohols has represented a main goal in asymmetric synthesis thanks to the broad availability of allyl metal compounds and to the extreme versatility of the products, which can be considered precursors of aldols, saturated alcohols, 1,3- and 1,4-diols. In this work we present a novel procedure for the synthesis of highly enantiomerically enriched homoallylic alcohols by the reaction of aldehydes with allyltributyltin in the presence of a catalytic amount of an (S)-(1 ,I'-binaphthalene)-2,2'-diol-titanium complex (BINOL-TiC12, S-1).

Catalytic asymmetric synthesis of homoallylic alcohols

Costa;Anna Luisa;
1993

Abstract

The synthesis of enantiomerically enriched homoallylic alcohols has represented a main goal in asymmetric synthesis thanks to the broad availability of allyl metal compounds and to the extreme versatility of the products, which can be considered precursors of aldols, saturated alcohols, 1,3- and 1,4-diols. In this work we present a novel procedure for the synthesis of highly enantiomerically enriched homoallylic alcohols by the reaction of aldehydes with allyltributyltin in the presence of a catalytic amount of an (S)-(1 ,I'-binaphthalene)-2,2'-diol-titanium complex (BINOL-TiC12, S-1).
1993
Inglese
115
15
7007
7008
https://www.scopus.com/inward/record.uri?eid=2-s2.0-12044252883&partnerID=40&md5=905a5a8cc003c1326594fd7c5f2f51e3
Chiral Lewis-Acids; Enantiomeric Purities; Aldehydes; Allylation; Complexes.
Cited by: 264
1
info:eu-repo/semantics/article
262
Costa; Anna Luisa;Piazza; Maria Giulia;Tagliavini; Emilio;Trombini; Claudio;UmaniRonchi; Achille
01 Contributo su Rivista::01.01 Articolo in rivista
none
File in questo prodotto:
Non ci sono file associati a questo prodotto.

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/20.500.14243/463789
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 252
  • ???jsp.display-item.citation.isi??? ND
social impact