One-pot preparation of N-(α-ferrocenylalkyl) substituted amino acid esters under acid-free conditions

The preparation of N-(α-ferrocenylalkyl) amino acid esters under neutral conditions by the reaction of in situ generated (α-ferrocenylalkyl)carbonates with amino acid esters is described. The method allows regioselective one-pot alkylation of a series of amino acid esters at the amino group, as well as diastereoselective preparation of ferrocenylalkyl substituted amino acid esters from (S)-(+)-α-ferrocenylethanol. © 2022

Authors
Shevaldina E.V.1 , Ambartsumyan A.A.1 , Pavlov A.A.1, 2 , Smol'yakov A.F. 1, 3 , Moiseev S.K.1
Language
English
Status
Published
Number
122384
Volume
972
Year
2022
Organizations
  • 1 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, ul. Vavilova 28, Moscow, 119991, Russian Federation
  • 2 D. Mendeleev University of Chemical Technology of Russia, Miusskaya pl., 9, Moscow, 125047, Russian Federation
  • 3 Peoples’ Friendship University of Russia (RUDN University), Miklukho-Maklaya Str. 6, Moscow, 117198, Russian Federation
Keywords
Acid-free conditions; Amino acid esters; Ferrocenylalkyl carbonates; Ferrocenylalkylation
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