405195-46-2Relevant academic research and scientific papers
Conformational switching caused by biphenyl substitution at the C α position: Ethyl 2-benzyl-2-(formylamino)-3-phenylpropionate and ethyl 3-(1,1′-biphenyl-4-yl)-2-(formylamino-2-(4-phenylbenzyl) propionate
Damodharan, Lakshminarasimhan,Pattabhi, Vasantha,Behera, Manoranjan,Kotha, Sambasivarao
, p. o527-o530 (2007/10/03)
The title compounds, C19H21NO3 and C 31H29NO3, are derivatives of α-aminoisobutyric acid, with benzyl and dibenzyl substitution. The pseudo-peptide formed by the N-formyl and ethyl ester su
Ethyl 2-formamido-2-(4-iodobenzyl)-3-(4-iodophenyl)propionate and ethyl 2-(3-bromobenzyl)-3-(3-bromophenyl)-2-formamidopropionate
Damodharan, Lakshminarasimhan,Pattabhi, Vasantha,Behera, Manoranjan,Kotha, Sambasivarao
, p. o216-o218 (2007/10/03)
The title compounds, C19H19I2NO3 and C19H19Br2NO3, are derivatives of α-aminoisobutyric acid with halogen substituents at the para and meta positions, respectively. The ethoxycarbonyl and formamide side chains attached to the Cαatom of the molecule adopt extended and folded conformations, respectively. The crystal structures are stabilized by N -H...O, C - H...O, C - Br...O and C - I...O interactions.
Synthesis of highly functionalised dibenzylglycine derivatives via the Suzuki-Miyaura coupling reaction
Kotha, Sambasivarao,Behera, Manoranjan,Kumar, Ramanatham Vinod
, p. 105 - 108 (2007/10/03)
Several α,α-dibenzylglycine (α-benzylphenylalanine) derivatives were prepared by alkylation of the ethyl isocyanoacetate with different benzyl bromide derivatives. Various aryl groups were introduced in the dibenzylglycine moiety via the Suzuki-Miyaura coupling reaction.
