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Volumn 62, Issue 43, 2006, Pages 10223-10236

1,3,4-Oxadiazole formation as traceless release in solid phase organic synthesis

Author keywords

Cyclative release; Dehydration; TFAA; Traceless linker; Transacylation

Indexed keywords

1,3,4 OXADIAZOLE DERIVATIVE; HYDRAZIDE DERIVATIVE; NITROGEN; ORGANIC COMPOUND; POLYMER;

EID: 33748545632     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.08.016     Document Type: Article
Times cited : (29)

References (41)
  • 1
    • 33748566489 scopus 로고    scopus 로고
    • For instance, recent publications:
  • 4
    • 33748527387 scopus 로고    scopus 로고
    • Lin, X.; Cui, S.; Wang, Y. Faming Zhuanli Shenqing Gongkai Shuomingshu 2003, 10 pp; CODEN: CNXXEV CN 1445219 A 20031001 Patent written in Chinese. Application: CN 2003-116520 20030417;
  • 6
    • 33748527680 scopus 로고    scopus 로고
    • Hennies, H.-H.; Sundermann, C.; Buschmann, H.; Sundermann, B. PCT Int. Appl. 2004, 49 pp; CODEN: PIXXD2 WO 2004024725;
  • 10
    • 33748573861 scopus 로고    scopus 로고
    • Recent syntheses of 1,3,4-oxadiazoles from 2-acyl hydrazides:
  • 18
    • 20044380367 scopus 로고    scopus 로고
    • Earlier reports on analogous solid phase Robinson-Gabriel synthesis of oxazoles:
    • Earlier reports on analogous solid phase Robinson-Gabriel synthesis of oxazoles:. Pulici M., Quartieri F., and Felder E.R. J. Comb. Chem. 7 (2005) 463-473
    • (2005) J. Comb. Chem. , vol.7 , pp. 463-473
    • Pulici, M.1    Quartieri, F.2    Felder, E.R.3
  • 19
    • 0001364113 scopus 로고
    • TFAA-mediated Bischler-Napieralski synthesis of isoquinolines:
    • TFAA-mediated Bischler-Napieralski synthesis of isoquinolines:. Nagubandi S., and Fodor G. Heterocycles 15 (1981) 165-177
    • (1981) Heterocycles , vol.15 , pp. 165-177
    • Nagubandi, S.1    Fodor, G.2
  • 21
    • 0013194371 scopus 로고
    • The mildness of this reducing agent allows it to be used even with proteins
    • Kikugawa Y., and Kawase M. Synth. Commun. 9 (1979) 49-52 The mildness of this reducing agent allows it to be used even with proteins
    • (1979) Synth. Commun. , vol.9 , pp. 49-52
    • Kikugawa, Y.1    Kawase, M.2
  • 22
    • 0021763364 scopus 로고
    • Analogous complexes have been reported to give reductions with hydrazides:
    • Wong W.S.D., Osuga D.T., and Feeney R.E. Anal. Biochem. 139 (1984) 58-67 Analogous complexes have been reported to give reductions with hydrazides:
    • (1984) Anal. Biochem. , vol.139 , pp. 58-67
    • Wong, W.S.D.1    Osuga, D.T.2    Feeney, R.E.3
  • 23
    • 33748543121 scopus 로고    scopus 로고
    • Miyamura, T.; Egashira, T.; Sano, M.; Bendiak, B. K.; Kato, I. PCT Int. Appl. 2002, 42 pp; CODEN: PIXXD2 WO 2002012254 A1 20020214; Application: WO 2001-JP6524 20010730. Priority: JP 2000-234508 20000802. CAN 136:184050 AN 2002:123019;
  • 31
    • 85082749528 scopus 로고
    • Oxadiazolinium-intermediates like proposed 12a-q have been reported earlier, for instance:
    • Oxadiazolinium-intermediates like proposed 12a-q have been reported earlier, for instance:. Molina P., Tarraga A., and Espinoas A. Synthesis (1988) 690-693
    • (1988) Synthesis , pp. 690-693
    • Molina, P.1    Tarraga, A.2    Espinoas, A.3
  • 39
    • 33748572469 scopus 로고    scopus 로고
    • Wang, Z. Y. U.S. Pat. Appl. Publ. 2003; 15 pp; CODEN: USXXCO US 2003010963 A1 20030116 CAN 138:114780 AN 2003:42708.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.