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SYNTHON CHEMISTRY: THEORETICAL STUDY ON THE FORMATION OF PROLINE, PHENYLANALINE AND TYROSINE.

Authors :
Surpateanu, Gheorghe
Georgescu, Ana-Maria
Nistor, Ileana-Denisa
Catalin Lungu, Neculai
Source :
Environmental Engineering & Management Journal (EEMJ); Jul2021, Vol. 20 Issue 7, p1111-1117, 7p
Publication Year :
2021

Abstract

According to the "synthon theory" on the formation of the first proteinogenic amino acids from three synthons: methylene, nitrene and carbon monoxide, at low temperatures, aziridinone would have formed. This, in contact with the same three synthons, forms the precursors of the 20 proteinogenic amino acids. These precursors, on contact with the components of the primary atmosphere, formed the first proteinogenic amino acids. The aim of this paper is to find the interradical reactions, which would have formed the precursors of proline, phenylalanine and tyrosine. The paper is a continuation of other studies on obtaining these amino acids in order to correlate them with their essential and non-essential character. As procedure, the quantitative results: enthalpies of formation, enthalpies of reaction, free energies, profile of reaction pathways were obtained by DFT calculations (B88-LYP). [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15829596
Volume :
20
Issue :
7
Database :
Supplemental Index
Journal :
Environmental Engineering & Management Journal (EEMJ)
Publication Type :
Academic Journal
Accession number :
151513498