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1
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33748566489
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For instance, recent publications:
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4
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33748527387
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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;
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6
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33748527680
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Hennies, H.-H.; Sundermann, C.; Buschmann, H.; Sundermann, B. PCT Int. Appl. 2004, 49 pp; CODEN: PIXXD2 WO 2004024725;
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10
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33748573861
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Recent syntheses of 1,3,4-oxadiazoles from 2-acyl hydrazides:
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12
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0037238110
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Park Y.-D., Kim J.-J., Chung H.-A., Kweon D.-H., Cho S.-D., Lee S.-G., and Yoon Y.-J. Synthesis (2003) 560-564
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(2003)
Synthesis
, pp. 560-564
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Park, Y.-D.1
Kim, J.-J.2
Chung, H.-A.3
Kweon, D.-H.4
Cho, S.-D.5
Lee, S.-G.6
Yoon, Y.-J.7
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18
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20044380367
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Earlier reports on analogous solid phase Robinson-Gabriel synthesis of oxazoles:
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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
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(2005)
J. Comb. Chem.
, vol.7
, pp. 463-473
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Pulici, M.1
Quartieri, F.2
Felder, E.R.3
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19
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0001364113
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TFAA-mediated Bischler-Napieralski synthesis of isoquinolines:
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TFAA-mediated Bischler-Napieralski synthesis of isoquinolines:. Nagubandi S., and Fodor G. Heterocycles 15 (1981) 165-177
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(1981)
Heterocycles
, vol.15
, pp. 165-177
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Nagubandi, S.1
Fodor, G.2
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21
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0013194371
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The mildness of this reducing agent allows it to be used even with proteins
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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
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(1979)
Synth. Commun.
, vol.9
, pp. 49-52
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Kikugawa, Y.1
Kawase, M.2
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22
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0021763364
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Analogous complexes have been reported to give reductions with hydrazides:
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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:
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(1984)
Anal. Biochem.
, vol.139
, pp. 58-67
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Wong, W.S.D.1
Osuga, D.T.2
Feeney, R.E.3
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23
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33748543121
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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;
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24
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0041333116
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Perdicchila D., Licandro E., Maiorana S., Baldoli C., and Giannini C. Tetrahedron 59 (2003) 7733-7742
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(2003)
Tetrahedron
, vol.59
, pp. 7733-7742
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Perdicchila, D.1
Licandro, E.2
Maiorana, S.3
Baldoli, C.4
Giannini, C.5
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25
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0242361217
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Bouget K., Aubin S., Delcros J.-G., Arlot-Bonnemains Y., and Baudy-Floc'h M. Bioorg. Med. Chem. (2003) 4881-4889
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(2003)
Bioorg. Med. Chem.
, pp. 4881-4889
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Bouget, K.1
Aubin, S.2
Delcros, J.-G.3
Arlot-Bonnemains, Y.4
Baudy-Floc'h, M.5
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27
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0037421005
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Hidaka K., Kimura T., Hayashi Y., McDaniel K.F., Dekhtyar T., Colletti L., and Kiso Y. Bioorg. Med. Chem. Lett. 13 (2003) 93-96
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(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 93-96
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Hidaka, K.1
Kimura, T.2
Hayashi, Y.3
McDaniel, K.F.4
Dekhtyar, T.5
Colletti, L.6
Kiso, Y.7
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31
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85082749528
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Oxadiazolinium-intermediates like proposed 12a-q have been reported earlier, for instance:
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Oxadiazolinium-intermediates like proposed 12a-q have been reported earlier, for instance:. Molina P., Tarraga A., and Espinoas A. Synthesis (1988) 690-693
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(1988)
Synthesis
, pp. 690-693
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Molina, P.1
Tarraga, A.2
Espinoas, A.3
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32
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33748579441
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A similar transacylation followed by oxadiazole formation was described by:
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A similar transacylation followed by oxadiazole formation was described by:. Hassan M.A., Mohamad M.M., Shiba S.A., Abou-El-Regal M.K., and Ali A.K. J. Saudi Chem. Soc. 3 (2003) 389-396
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(2003)
J. Saudi Chem. Soc.
, vol.3
, pp. 389-396
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Hassan, M.A.1
Mohamad, M.M.2
Shiba, S.A.3
Abou-El-Regal, M.K.4
Ali, A.K.5
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35
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0342520728
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Raj S.S.S., Yamin B.M., Boshaala A.M.A., Tarafder M.T.H., Crouse K.A., and Fun H.-K. Acta Crystallogr., Sect. C 56 (2000) 1011-1012
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(2000)
Acta Crystallogr., Sect. C
, vol.56
, pp. 1011-1012
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Raj, S.S.S.1
Yamin, B.M.2
Boshaala, A.M.A.3
Tarafder, M.T.H.4
Crouse, K.A.5
Fun, H.-K.6
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33748572469
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Wang, Z. Y. U.S. Pat. Appl. Publ. 2003; 15 pp; CODEN: USXXCO US 2003010963 A1 20030116 CAN 138:114780 AN 2003:42708.
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