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1
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12344337315
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For reviews of Pd catalyzed reaction, see:
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For reviews of Pd catalyzed reaction, see:. Schlummer B., and Scholz U. Adv. Synth. Catal. 346 (2004) 1599
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(2004)
Adv. Synth. Catal.
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Schlummer, B.1
Scholz, U.2
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3
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0345708168
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For reviews of Cu catalyzed reactions, see
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For reviews of Cu catalyzed reactions, see. Ley S.V., and Thomas A.W. Angew. Chem., Int. Ed. 42 (2003) 5400
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(2003)
Angew. Chem., Int. Ed.
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Ley, S.V.1
Thomas, A.W.2
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6
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0003607021
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For a general review of heterocycles see:. Katritzky A.R., and Rees C.W. (Eds), Elsevier, Oxford
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For a general review of heterocycles see:. In: Katritzky A.R., and Rees C.W. (Eds). Comprehensive Heterocyclic Chemistry II (1996), Elsevier, Oxford
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(1996)
Comprehensive Heterocyclic Chemistry II
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7
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14844330054
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Selected examples:
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Selected examples:. Shen Q., Shekhar S., Stambuli J.P., and Hartwig J.F. Angew. Chem., Int. Ed. 44 (2005) 1371
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Shen, Q.1
Shekhar, S.2
Stambuli, J.P.3
Hartwig, J.F.4
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11
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0035963004
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Madar D.J., Kopecka H., Pireh D., Pease J., Pliushchev M., Sciotti R.J., Wiedeman P.E., and Djuric S.W. Tetrahedron Lett. 42 (2001) 3681
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(2001)
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Madar, D.J.1
Kopecka, H.2
Pireh, D.3
Pease, J.4
Pliushchev, M.5
Sciotti, R.J.6
Wiedeman, P.E.7
Djuric, S.W.8
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12
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0038579438
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Huang X., Anderson K.W., Zim D., Jiang L., Klapars A., and Buchwald S.L. J. Am. Chem. Soc. 125 (2003) 6653
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Huang, X.1
Anderson, K.W.2
Zim, D.3
Jiang, L.4
Klapars, A.5
Buchwald, S.L.6
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17
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0032501446
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Ma D., Zhang Y., Yao J., Wu S., and Tao F. J. Am. Chem. Soc. 120 (1998) 12459
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Ma, D.1
Zhang, Y.2
Yao, J.3
Wu, S.4
Tao, F.5
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20
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33746186589
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note
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All microwave reactions were performed using a Personal Chemistry Emrys™ Optimizer in a septa capped 0.50-2 mL Biotage™ microwave vial with magnetic stirring. Power required to maintain target temperature was controlled by Emrys™ Optimizer Software.
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21
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33746247426
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note
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Samples were purified by preparative HPLC on a Waters Nova-Pak HR C18 6 μm 60 Å Prep-Pak cartridge column (40 mm × 100 mm). A gradient of acetonitrile (A) and 0.1% trifluoroacetic acid in water (B) was used, at a flow rate of 70 mL/min (0-0.5 min 10% A, 0.5-12.0 min linear gradient 10-95% A, 12.0-15.0 min 95% A, 15.0-17.0 min linear gradient 95-10% A). Samples were injected in 2.5 mL of DMSO/MeOH (1:1).
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22
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0030027833
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Brickner S.J., Hutchinson D.K., Barbachyn M.R., Manninen P.R., Ulanowicz D.A., Garmon S.A., Grega K.C., Hendges S.K., Toops D.S., Ford C.W., and Zurenko G.E. J. Med. Chem. 36 (1996) 673
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(1996)
J. Med. Chem.
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, pp. 673
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Brickner, S.J.1
Hutchinson, D.K.2
Barbachyn, M.R.3
Manninen, P.R.4
Ulanowicz, D.A.5
Garmon, S.A.6
Grega, K.C.7
Hendges, S.K.8
Toops, D.S.9
Ford, C.W.10
Zurenko, G.E.11
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