77426-68-7Relevant articles and documents
One-pot synthesis of α-amino acids based on free radical-mediated carbon-carbon bond formation
Miyabe, Hideto,Yoshioka, Naoko,Ueda, Masafumi,Naito, Takeaki
, p. 3659 - 3660 (1998)
The one-pot reaction of 2-hydroxy-2-methoxyacetic acid methyl ester with benzyloxyamine and an alkyl radical provided a convenient method for preparing the protected α-amino acids via a carbon-carbon bond formation by intermolecular carbon radical additio
Zinc-mediated carbon radical addition to glyoxylic imines in aqueous media for the synthesis of α-amino acids
Ueda, Masafumi,Miyabe, Hideto,Sugino, Hisako,Naito, Takeaki
, p. 1124 - 1128 (2007/10/03)
The addition of carbon radicals to glyoxylic imines was studied using zinc dust as a radical initiator. The zinc-mediated radical reaction of glyoxylic oxime ethers and hydrazones proceeded smoothly to give the alkylated products via a carbon-carbon bond-
Zinc-mediated radical reaction of glyoxylic oxime ether and hydrazone in aqueous media: Asymmetric synthesis of α-amino acids
Ueda, Masafumi,Miyabe, Hideto,Nishimura, Azusa,Sugino, Hisako,Naito, Takeaki
, p. 2857 - 2859 (2007/10/03)
Alkyl radical addition to glyoxylic oxime ether and hydrazone in aqueous media was studied using zinc dust as a radical initiator. The zinc-mediated radical reaction of the hydrazone bearing a chiral camphorsultam provided the corresponding alkylated prod
