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Volumn 49, Issue 35, 2008, Pages 5129-5132

Stable organogels derived from triazines functionalized with chiral α-amino acid derivatives

Author keywords

Amino acids; Hydroxamic acids; Melamine; Organogel; Triazine

Indexed keywords

ALKANE DERIVATIVE; AMINO ACID DERIVATIVE; AROMATIC COMPOUND; GELLING AGENT; MELAMINE; ORGANIC COMPOUND; SOLVENT; TRIAZINE DERIVATIVE;

EID: 47049126859     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.06.101     Document Type: Article
Times cited : (18)

References (34)
  • 2
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    • and references cited therein
    • Sangeetha N.M., and Maitra U. Chem. Soc. Rev. 34 (2005) 821-836 and references cited therein
    • (2005) Chem. Soc. Rev. , vol.34 , pp. 821-836
    • Sangeetha, N.M.1    Maitra, U.2
  • 15
    • 33748285257 scopus 로고    scopus 로고
    • While this manuscript was being revised another article on diaminotriazine gelators was published
    • Lebel O., Perron M., Maris T., Zalzal S.F., Nanci A., and Wuest J.D. Chem. Mater. 18 (2006) 3616-3626 While this manuscript was being revised another article on diaminotriazine gelators was published
    • (2006) Chem. Mater. , vol.18 , pp. 3616-3626
    • Lebel, O.1    Perron, M.2    Maris, T.3    Zalzal, S.F.4    Nanci, A.5    Wuest, J.D.6
  • 17
    • 16244391781 scopus 로고    scopus 로고
    • For other recent examples of organogels see:
    • For other recent examples of organogels see:. Shirakawa M., Fujita N., and Shinkai S. J. Am. Chem. Soc. 127 (2005) 4164-4165
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 4164-4165
    • Shirakawa, M.1    Fujita, N.2    Shinkai, S.3
  • 28
    • 1342323920 scopus 로고    scopus 로고
    • For other examples of α-amino acid-based organogelators see: See also Refs. 8c,e,h
    • For other examples of α-amino acid-based organogelators see:. Suzuki M., Yumoto M., Kimura M., Shirai H., and Hanabusa K. Helv. Chim. Acta 87 (2004) 1-10 See also Refs. 8c,e,h
    • (2004) Helv. Chim. Acta , vol.87 , pp. 1-10
    • Suzuki, M.1    Yumoto, M.2    Kimura, M.3    Shirai, H.4    Hanabusa, K.5
  • 29
    • 47049129967 scopus 로고    scopus 로고
    • note
    • Benzene actually gave organogels with 3a at 2% w/w, but this solvent was not extensively investigated due to its toxicity.
  • 31
    • 8744260641 scopus 로고    scopus 로고
    • For recent articles discussing the effect of stereochemistry and stereochemical purity on the gel-forming capacity of small molecular entities:
    • For recent articles discussing the effect of stereochemistry and stereochemical purity on the gel-forming capacity of small molecular entities:. Aoki K., Kudo M., and Tamaoki N. Org. Lett. 6 (2004) 4009-4012
    • (2004) Org. Lett. , vol.6 , pp. 4009-4012
    • Aoki, K.1    Kudo, M.2    Tamaoki, N.3
  • 33
    • 47049118195 scopus 로고    scopus 로고
    • note
    • Attempts to study the hydrogen-bonding behaviour of amide and hydroxamic groups by means of FTIR of the organogels as a function of the temperature did not provide conclusive results.
  • 34
    • 0034731020 scopus 로고    scopus 로고
    • For a detailed discussion of this kind of rheological measurements see:
    • For a detailed discussion of this kind of rheological measurements see:. Menger F.M., and Caran K.L. J. Am. Chem. Soc. 122 (2000) 11679-11691
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 11679-11691
    • Menger, F.M.1    Caran, K.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.