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Volumn 71, Issue 26, 2006, Pages 9791-9796

Heterogeneous diazo-transfer reaction: A facile unmasking of azide groups on amine-functionalized insoluble supports for solid-phase synthesis

Author keywords

[No Author keywords available]

Indexed keywords

IONS; MONOMERS; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 33845955004     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0618122     Document Type: Article
Times cited : (29)

References (61)
  • 4
    • 10044296189 scopus 로고    scopus 로고
    • Attachments of Nucleosides to Solid Supports
    • Beaucage, S. L, Bergstrom, D. E, Glick, G. D, Jones, R. A, Eds, John Wiley: New York
    • Pon, R. T. Attachments of Nucleosides to Solid Supports. In Current Protocols in Nucleic Acids Chemistry; Beaucage, S. L., Bergstrom, D. E., Glick, G. D., Jones, R. A., Eds.; John Wiley: New York, 1999; pp 287-298.
    • (1999) In Current Protocols in Nucleic Acids Chemistry , pp. 287-298
    • Pon, R.T.1
  • 15
    • 0003917975 scopus 로고
    • For reviews on aryl azides as photoaffinity labels and references therein, see: a, Scriven, E. F. V, Ed, Academic Press: Orlando
    • For reviews on aryl azides as photoaffinity labels and references therein, see: (a) Bayley, H.; Staros, J. V. In Azides and Nitrenes; Scriven, E. F. V., Ed.; Academic Press: Orlando, 1984; pp 433-490.
    • (1984) Azides and Nitrenes , pp. 433-490
    • Bayley, H.1    Staros, J.V.2
  • 16
    • 0018853583 scopus 로고    scopus 로고
    • Applications of Photochemistry in Probing Biological Targets. In Annals of the New York Academy of Sciences; Tometsko, A. M., Richards, F. M., Eds.; New York Academy of Sciences: New York, 1980; 346.
    • (b) Applications of Photochemistry in Probing Biological Targets. In Annals of the New York Academy of Sciences; Tometsko, A. M., Richards, F. M., Eds.; New York Academy of Sciences: New York, 1980; Vol. 346.
  • 23
    • 0037099395 scopus 로고    scopus 로고
    • Numerous examples of click chemistry have appeared in the literature. Cited here are two pioneering examples: (a) Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. Angew. Chem., Int. Ed. 2002, 41, 2596.
    • Numerous examples of click chemistry have appeared in the literature. Cited here are two pioneering examples: (a) Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. Angew. Chem., Int. Ed. 2002, 41, 2596.
  • 25
    • 0348109450 scopus 로고    scopus 로고
    • For reviews on the application of click chemistry, see: a
    • For reviews on the application of click chemistry, see: (a) Kolb, H. C.; Sharpless, K. B. DDT 2003, 8, 1128.
    • (2003) DDT , vol.8 , pp. 1128
    • Kolb, H.C.1    Sharpless, K.B.2
  • 41
    • 0001265391 scopus 로고
    • For examples, see: a
    • For examples, see: (a) Ruff, J. K. Inorg. Chem. 1965, 4, 567.
    • (1965) Inorg. Chem , vol.4 , pp. 567
    • Ruff, J.K.1
  • 50
    • 33845927134 scopus 로고    scopus 로고
    • We are grateful to the reviewers for suggesting the substitution of dichloromethane with nonhalogenated solvents as an alternative way to minimize the potential danger of explosion during the synthesis of triflyl azide
    • (j) We are grateful to the reviewers for suggesting the substitution of dichloromethane with nonhalogenated solvents as an alternative way to minimize the potential danger of explosion during the synthesis of triflyl azide.
  • 52
    • 0347192214 scopus 로고    scopus 로고
    • -1. Lieber, E.; Ramachandra Rao, C. N.; Chao, T. S.; Hoffman, C. W. W. Anal. Chem. 1957, 29, 916.
    • -1. Lieber, E.; Ramachandra Rao, C. N.; Chao, T. S.; Hoffman, C. W. W. Anal. Chem. 1957, 29, 916.
  • 58
    • 33845931158 scopus 로고    scopus 로고
    • Applied Biosystems Users Bulletin. DNA Synthesizer, Model 380/ 381, Issue 13, Revised April 1, 1987: p 12.
    • Applied Biosystems Users Bulletin. DNA Synthesizer, Model 380/ 381, Issue 13, Revised April 1, 1987: p 12.
  • 59
    • 33845933981 scopus 로고    scopus 로고
    • DNA syntheses on an Expedite DNA synthesizer were performed at the Yale University Keck Oligo facility
    • DNA syntheses on an Expedite DNA synthesizer were performed at the Yale University Keck Oligo facility.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.