Mannich-type reactions of in situ generated N-acyliminium ions from α-amido p-tolylsulfones with silyl enolates

Bulletin of the Korean Chemical Society

Volumn 32, Issue 10, 2011, Pages 3738-3742

  Lee, Sang Hyeup ^a   Kadam, Santosh T ^a  

^a Catholic University of Daegu   (South Korea)

Author keywords

Amido p tolylsulfone; Cbz Protected amino ketone; Mannich type reaction; N Acyliminium ion

Indexed keywords

ALIPHATIC ALDEHYDES; AMINO ESTERS; CATALYTIC AMOUNTS; ENOL ESTERS; ENOLATES; GOOD YIELD; IN-SITU; MANNICH-TYPE REACTIONS; MILD REACTION CONDITIONS; N-ACYLIMINIUM ION; SILYL ENOL ETHERS;

ALDEHYDES; BISMUTH; ESTERIFICATION; ESTERS; ETHERS; KETONES;

IONS;

EID: 80054973813     PISSN: 02532964     EISSN: 12295949     Source Type: Journal    
DOI: 10.5012/bkcs.2011.32.10.3738     Document Type: Article

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