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Volumn 130, Issue 40, 2008, Pages 13225-13227

Addressing mechanistic issues in the coupling of isonitriles and carboxylic acids: Potential routes to peptidic constructs

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLIC ACID DERIVATIVE; FORMIMIDATE CARBOXYLATE MIXED ANHYDRIDE; ISONITRILE DERIVATIVE; PEPTIDE; UNCLASSIFIED DRUG;

EID: 53549120657     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja804709s     Document Type: Article
Times cited : (63)

References (32)
  • 6
    • 26844537872 scopus 로고    scopus 로고
    • For reviews, see: c
    • For reviews, see: (c) Banfi, L.; Riva, R. Org. React. 2005, 65, 1.
    • (2005) Org. React , vol.65 , pp. 1
    • Banfi, L.1    Riva, R.2
  • 12
    • 45749083425 scopus 로고    scopus 로고
    • Recently, Rebek and colleagues described the apparent intervention of a FCMA in the context of molecular encapsulation: (a) Hou, J-L.; Ajami, D.; Rebek, J., Jr J. Am. Chem. Soc. 2008, 130, 7810.
    • Recently, Rebek and colleagues described the apparent intervention of a FCMA in the context of molecular encapsulation: (a) Hou, J-L.; Ajami, D.; Rebek, J., Jr J. Am. Chem. Soc. 2008, 130, 7810.
  • 14
    • 53549104679 scopus 로고    scopus 로고
    • The tendency of anti and syn imidic-carboxylic mixed anhydrides to rearrange to imides and the interconversion of these isomers have been discussed; see ref 7
    • The tendency of anti and syn imidic-carboxylic mixed anhydrides to rearrange to imides and the interconversion of these isomers have been discussed; see ref 7.
  • 23
    • 43249113921 scopus 로고    scopus 로고
    • N-methyl peptides possess interesting biological profiles: (a) Subtelny, A. O.; Hartman, M. C. T.; Szostak, J. W. J. Am. Chem. Soc. 2008, 130, 6131.
    • N-methyl peptides possess interesting biological profiles: (a) Subtelny, A. O.; Hartman, M. C. T.; Szostak, J. W. J. Am. Chem. Soc. 2008, 130, 6131.
  • 25
    • 11144336770 scopus 로고    scopus 로고
    • With our methodology, such scaffolds can be readily reached as shown in ref 1a
    • (c) Aurelio, L.; Brownlee, R. T. C.; Hughes, A. B. Chem. Rev. 2004, 104, 5823. With our methodology, such scaffolds can be readily reached as shown in ref 1a.
    • (2004) Chem. Rev , vol.104 , pp. 5823
    • Aurelio, L.1    Brownlee, R.T.C.2    Hughes, A.B.3
  • 28
    • 53549125187 scopus 로고    scopus 로고
    • 3N).
    • 3N).
  • 29
    • 53549107684 scopus 로고    scopus 로고
    • Compounds 17 and 18 are a diastereomeric mixture of trans/cis isomers, as is 23.
    • Compounds 17 and 18 are a diastereomeric mixture of trans/cis isomers, as is 23.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.