An efficient SbCl3-metal system for allylation, reduction and acetalization of aldehydes

Tetrahedron

Volumn 46, Issue 9, 1990, Pages 3315-3320

  Wei, Bo Wang ^a   Li Lan, Shi ^a   Yao Zeng, Huang ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000142335     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)85467-3     Document Type: Article

References (21)

1. α-Enone by the Reaction of Aldehyde and α-Bromoketone with Tri-n-Butylstibine
2. Tributylstibine-mediated olefination of carbonyl compounds with bromomalonic ester and with dibromomalonic ester?A possible pathway through a stibonium ylide via halophilic initiation by tertiary stibines
3. Carbon-carbon bond formation with metallic manganese.
4. Lead-promoted allylation of carbonyl compounds with allyl bromide.
5. Highly selective formation of 1-phenylethanol by indirect electroreduction of acetophenone on a lead cathode in the presence of catalytic amounts of antimony(III) chloride.