Synthesis of novel chiral C 2 symmetric diaza 18 crown 6 ether derivatives and their enantioselective recognition of amino acid derivatives

Turgut, Yılmaz; DEMİREL, NADİR; Hoşgören, Halil

doi:10.1007/s10847-005-3125-1

Synthesis of novel chiral C 2 symmetric diaza 18 crown 6 ether derivatives and their enantioselective recognition of amino acid derivatives

Yazarlar (3)

Yılmaz Turgut
Dicle Üniversitesi, Türkiye

Prof. Dr. Nadir DEMİREL Dicle Üniversitesi, Türkiye

Halil Hoşgören
Dicle Üniversitesi, Türkiye

Makale Türü	Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı	Journal of Inclusion Phenomena
Dergi ISSN	0923-0750
Dergi Tarandığı Indeksler	SCI-Expanded
Makale Dili	İngilizce	Basım Tarihi	01-2006
Cilt / Sayı / Sayfa	54 / 1 / 29–33	DOI	10.1007/s10847-005-3125-1

Özet

New chiral diaza-18-crown-6 ether derivatives, 5 and 6 were synthesized from (R)-(-)-2-amino-1-bütanol. These chiral artificial receptors exhibit pronounced chiral recognition toward the enantiomers of L- and D- amino acid derivatives. The highest enantioselectivity was observed in the case of Trp-OMe·HCl (KD/KL = 12.5). © Springer 2006.

Anahtar Kelimeler

Amino acid | Chiral aza crown ether | Complexation | Molecular recognition

BM Sürdürülebilir Kalkınma Amaçları

Atıf Sayıları
WoS	12
SCOPUS	11
Google Scholar	13

Synthesis of novel chiral C 2 symmetric diaza 18 crown 6 ether derivatives and their enantioselective recognition of amino acid derivatives

Synthesis of novel chiral C 2 symmetric diaza 18 crown 6 ether derivatives and their enantioselective recognition of amino acid derivatives

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