Reactions of α-substituted glycine derivatives with stannanes
CJ Easton, SC Peters
Index: Easton; Peters Tetrahedron Letters, 1992 , vol. 33, # 38 p. 5581 - 5584
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Citation Number: 8
Abstract
Abstract α-Benzoyloxy-and α-methoxy-substituted glycine derivatives are more stable than the corresponding bromides, yet they undergo analogous reactions with stannanes. Their reactions with mixtures of hexabutylditin and dialkyl disulphides give α-alkylthio-substituted
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