Synthesis of α-alkyl and α-functionalize
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P. Bey; J.P. Vevert
📂
Article
📅
1977
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Elsevier Science
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French
⚖ 186 KB
As part of our program aimed at the design of specific enzyme inhibitors, we have been interested in the synthesis of a-alkyl substituted-u-amino acids of type 1 (Y -H or heteroatom functions). R CH3 The classical route to a-alkyl substituted-a-amino acids consists of a Bucherer or a Strecker reacti