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Newkome, G.R.1
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Moorefield, C.N.5
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4
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0032513361
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Wang J., Yoo Y., Gao C., Takeuchi I., Sun X., Chang H., Xiang X.-D., and Schultz P.G. Science 279 (1998) 1712-1714
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13
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0026656122
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Frank R. Tetrahedron 48 (1992) 9217-9232
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Frank, R.1
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14
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0036721834
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For recent reviews of SPOT-synthesis, see:
-
For recent reviews of SPOT-synthesis, see:. Frank R. J. Immunol. Methods 267 (2002) 13-26
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(2002)
J. Immunol. Methods
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Frank, R.1
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16
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33645970084
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note
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2).
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-
-
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19
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33646005407
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For selected examples, see:
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-
-
-
22
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0033522834
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Ast T., Heine N., Germeroth L., Schneider-Mergener J., and Wenschuh H. Tetrahedron Lett. 40 (1999) 4317-4318
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Ast, T.1
Heine, N.2
Germeroth, L.3
Schneider-Mergener, J.4
Wenschuh, H.5
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23
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33646000186
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For recent commentaries on MW-assisted combinatorial chemistry, see:
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-
-
-
26
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33645964841
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For recent reviews on MW-assisted organic chemistry, see:
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-
-
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28
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12344305106
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Santagada V., Frecentese F., Perissutti E., Favretto L., and Caliendo G. QSAR Comb. Sci. 23 (2004) 919-944
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QSAR Comb. Sci.
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Santagada, V.1
Frecentese, F.2
Perissutti, E.3
Favretto, L.4
Caliendo, G.5
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32
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33947091567
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Amine functionalization levels were determined by derivatization of support 3 with Fmoc-OSu, cleavage of the N-Fmoc group with piperidine, and quantitation of released fulvene product using UV spectroscopy (at 296 nm) according to standard procedures. See:
-
Amine functionalization levels were determined by derivatization of support 3 with Fmoc-OSu, cleavage of the N-Fmoc group with piperidine, and quantitation of released fulvene product using UV spectroscopy (at 296 nm) according to standard procedures. See:. Carpino L.A., and Han G.Y. J. Org. Chem. 37 (1972) 3404-3409
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Carpino, L.A.1
Han, G.Y.2
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33
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0034222020
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Scharn D., Wenschuh H., Reineke U., Schneider-Mergener J., and Germeroth L. J. Comb. Chem. 2 (2000) 361-369
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Scharn, D.1
Wenschuh, H.2
Reineke, U.3
Schneider-Mergener, J.4
Germeroth, L.5
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34
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33645988427
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For further information about this commercial MW reactor system, see:
-
For further information about this commercial MW reactor system, see:. http://www.milestonesci.com/index2.php
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-
-
-
35
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33645991410
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-
note
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Performing this MW-assisted reaction using automated temperature control during the reaction was not possible due to the low solvent volumes used.
-
-
-
-
36
-
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33645973473
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-
note
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Linker loading on support determined by quantifying the amount of free amine (using standard UV Fmoc analysis; see Ref. 22) on the support before and after coupling of the pro-linker unit and its reduction. The difference between these two values was indicative of the amount of linker coupled to the support.
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-
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43
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33645958163
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See Ref. 5;
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-
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46
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22244483070
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Tu S., Li T., Shi F., Fang F., Zhu S., Wei X., and Zong Z. Chem. Lett. 34 (2005) 732-733
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Chem. Lett.
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, pp. 732-733
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Tu, S.1
Li, T.2
Shi, F.3
Fang, F.4
Zhu, S.5
Wei, X.6
Zong, Z.7
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47
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0345580223
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Grosche P., Höltzel A., Walk T.B., Trautwein A.W., and Jung G. Synthesis 11 (1999) 1961-1970
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(1999)
Synthesis
, vol.11
, pp. 1961-1970
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-
Grosche, P.1
Höltzel, A.2
Walk, T.B.3
Trautwein, A.W.4
Jung, G.5
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48
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33645998649
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-
For further information about this commercial MW reactor system, see:
-
For further information about this commercial MW reactor system, see:. http://www.cem.com/
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-
-
-
49
-
-
33646016481
-
-
note
-
Purity and yields determined by integration of HPLC spectra at 254 nm and comparison to a UV calibration curve generated for triarylpyridine 16r. See Supplementary material.
-
-
-
-
50
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-
20044376318
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For a recent commentary on this process, see:
-
For a recent commentary on this process, see:. Alcázar J. J. Comb. Chem. 7 (2005) 353-355
-
(2005)
J. Comb. Chem.
, vol.7
, pp. 353-355
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Alcázar, J.1
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51
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0035003754
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Padilla-Tosta M.E., Lloris J.M., Martinez-Màñez R., Marcos M.D., Miranda M.A., Pardo T., Sancenón F., and Soto J. Eur. J. Inorg. Chem. (2001) 1475-1482
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Eur. J. Inorg. Chem.
, pp. 1475-1482
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Padilla-Tosta, M.E.1
Lloris, J.M.2
Martinez-Màñez, R.3
Marcos, M.D.4
Miranda, M.A.5
Pardo, T.6
Sancenón, F.7
Soto, J.8
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