126824-96-2Relevant articles and documents
A Novel Stereoselective Route to β-Lactams: Diastereoselective Synthesis of a Key Intermediate for Carbapenem Antibiotic (+)-PS-5
Miyata, Okiko,Fujiwara, Yoko,Ninomiya, Ichiya,Naito, Takeaki
, p. 2861 - 2862 (2007/10/02)
A combination of stereoselective addition of thiophenol to olefins and subsequent substitution of the corresponding sulfonium group with an O-alkylhydroxamate anion has provided a new practical and stereoselective method for the construction of β-lactams which has been successfully applied to the formal asymmetric synthesis of the carbapenem antibiotic (+)-PS-5 1.
Stereospecific nucelophilic addition reaction of thiophenol to α, β-unsaturated esters
Miyata,Shinada,Naito,Ninomiya
, p. 3158 - 3160 (2007/10/02)
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