Asymmetric synthesis of β-hydroxythioacetamides mediated by enantiomerically pure sulphiny1 derivatives

Tetrahedron

Volumn 41, Issue 21, 1985, Pages 4929-4936

  Cinquini, Mauro ^a   Manfredi, Amedea ^a   Molinari, Henriette ^a   Restelli, Angelo ^a  

^a CNR   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0006582405     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)96733-X     Document Type: Article

References (19)

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2. Asymmetric Synthesis Using Nucleophilic Reagents Containing a Chiral Sulfoxide Group
3. Optically Active t-Butyl 2-(p-Tolylsulfinyl)propionate and -butyrate: Synthesis and Reactivity in Aldol-type Condensations
4. Application of chiral sulfoxides in asymmetric synthesis: the enantiospecific synthesis of the chroman ring of .alpha.-tocopherol (vitamin E)
5. Chiral homoenolate anion equivalents: synthesis of optically pure 5-substituted furan-2(5H)-ones
6. Optically Active 2-(Arylsulfinylmethyl)-oxazolines, Chiral Enol Acetate Equivalents in Aldol-Type Condensations
7. Double aldol condensation: stereoselective synthesis of masked and un-masked ?,??-dihydroxyketones
8. Recent Advances in Stereochemical Control: Multiple Asymmetric Induction
9. 777. Antituberculous compounds. Part X. Some reactions of quaternary compounds derived from NN-disubstituted thioamides
10. Direkte Darstellung von Thioamiden aus Säurechloriden und Aminen
11. Conversion of thioamides and N 2-acyl-N 1-methyl-N 1-thioacylhydrazines into amides and N 1 N 2-diacyl-N 1-methylhydrazines by trimethyloxonium fluoroborate