58456-27-2Relevant academic research and scientific papers
Ultrasound mediated synthesis of 2-amino-1,3-selenazoles derived from Fmoc/Boc/Z-α-amino acids
Lalithamba, Haraluru S.,Narendra,Naik, Shankar A.,Sureshbabu, Vommina V.
scheme or table, p. 77 - 90 (2010/12/19)
A simple and efficient one-pot synthesis of Fmoc/Boc/Z-amino acid derived 2-amino-1,3-selenazoles by the condensation of Nα-urethane protected amino acid derived bromomethyl ketones with selenourea under the influence of ultrasound has been described. Insertion of 2-amino-1,3-selenazole moiety in the side chains of Asp and Glu has also been achieved following the similar protocol. ARKAT USA, Inc.
A Convenient Differential Protection Strategy for Functional Group Manipulation of Aspartic and Glutamic Acids
Scholtz, John M.,Bartlett, Paul A.
, p. 542 - 544 (2007/10/02)
Procedures are provided for selective protection of the α-carboxyl groups of aspartic and glutamic acids via the 5-oxazolidinones 2.A convenient synthesis of a differentially protected derivative of (S)-2,3-diaminopropanoic acid, 3, is described, along wi
L-α-AMINOADIPIC ACID FROM L-GLUTAMIC ACID
Pellicciari, Roberto,Natalini, Benedetto,Marinozzi, Maura
, p. 1707 - 1714 (2007/10/02)
A convenient procedure for the preparation of L-α-aminoadipic acid from L-glutamic acid is described.
An Asymmetric Synthesis of cis-5-Alkylproline Derivatives
Ho, Teresa L.,Gopalan, Balasubramanian,Nestor, John J.
, p. 2405 - 2408 (2007/10/02)
We have developed a versatile and convenient synthesis of cis-5-alkylprolinamides.Protection/activation of the α-carboxylic acid function of N-benzyloxycarbonyl-L-glutamic acid (Z-L-Glu-OH) by reaction with H2CO to form an N-Z-oxazolidinone ring allowed t
