2010
DOI: 10.1590/s0100-40422010000500031
|View full text |Cite
|
Sign up to set email alerts
|

Evolução biomolecular homoquiral: a origem e a amplificação da quiralidade nas moléculas da vida

Abstract: Recebido em 22/10/09; aceito em 22/12/09; publicado na web em 6/5/10 HOMOCHIRAL BIOMOLECULAR EVOLUTION. THE ORIGIN AND THE AMPLIFICATION OF CHIRALITY IN LIFE MOLECULES. The fact that biologically relevant molecules exist only as one of the two enantiomers is a fascinating example of complete symmetry breaking of chirality and has long intrigued our curiosity. The origin of this selective chirality has remained a fundamental enigma with regard to the origin of life since the time of Pasteur, 160 years ago. The … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
10
0
2

Year Published

2018
2018
2022
2022

Publication Types

Select...
3
1

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(12 citation statements)
references
References 54 publications
(58 reference statements)
0
10
0
2
Order By: Relevance
“…Chiral calixarenes are a class of important host compounds which have wide applications in chiral recognition, enantiomer separation, and asymmetrical catalysis [70][71][72]. Calix [4]arene compounds are the most investigated molecules due to their stable bowl-shaped conformation and easy derivatization. The intramolecular cavities of calixarenes are known to be able to selectively interact with structurally complementary molecular species for molecular recognition purposes.…”
Section: Chiral Recognition Layer From Supermolecular Structuresmentioning
confidence: 99%
See 2 more Smart Citations
“…Chiral calixarenes are a class of important host compounds which have wide applications in chiral recognition, enantiomer separation, and asymmetrical catalysis [70][71][72]. Calix [4]arene compounds are the most investigated molecules due to their stable bowl-shaped conformation and easy derivatization. The intramolecular cavities of calixarenes are known to be able to selectively interact with structurally complementary molecular species for molecular recognition purposes.…”
Section: Chiral Recognition Layer From Supermolecular Structuresmentioning
confidence: 99%
“…Akpinar et al reported a simple and quick chiral discrimination strategy for ascorbic acid (AA) enantiomers based on calixarenes films (Figure 6) [76]. A chiral calix [4]arene-bearing chiral phenyl glycinol moiety on the lower rim and a thiol moiety on the upper rim were deposited on the gold surface of the QCM electrode. The chiral calixarene film exhibited good and more than doubled selectivity towards ʟ-AA.…”
Section: Chiral Recognition Layer From Supermolecular Structuresmentioning
confidence: 99%
See 1 more Smart Citation
“…No entanto, nem todos os L-aminoácidos são levógiros porque L (Figura 2.3) e D (Figura 2.4) referem-se apenas à configuração absoluta dos quatro substituintes em torno do carbono quiral, não às propriedades óticas da molécula [7]. Embora os aminoácidos sintetizados por processos não biológicos sejam misturas dos dois enantiômeros L e D, a vida como se conhece faz uso da homoquiralidade e os L-aminoácidos dominam em praticamente 100% dos casos [8], [9].…”
Section: Aminoácidosunclassified
“…Além disso, a Figura (4.34-a) também exibe uma extrapolação de seções transversais de destruição de ALA em 5 − 10 5 eV (linha sólida) obtidas a partir do ajuste da função da equação (4-9). Um gráfico Φ SW σ ef d × E foi gerado para o cálculo da taxa de destruição k definida na equação (3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15), sendo apresentada na Figura (4.34-b).…”
Section: Cálculo Do Tempo De Meia-vida Da Alaninaunclassified