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1
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0000860751
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Combinatorial chemistry
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[1] For reviews, see: (a) Combinatorial chemistry. In: Szostak JW, Ed. Chem. Rev. 1997;97:347-509.
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(1997)
Chem. Rev.
, vol.97
, pp. 347-509
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Szostak, J.W.1
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10
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0000315424
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Trost BM, Fleming I, editors. Oxford: Pergamon Press
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[4] (a) Curran DP. In: Trost BM, Fleming I, editors. Comprehensive Organic Synthesis. Oxford: Pergamon Press, 1991:779-831.
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(1991)
Comprehensive Organic Synthesis
, pp. 779-831
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Curran, D.P.1
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16
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0001491565
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(e) Toru T, Watanabe Y, Mase N, Tsusaka M, Hayakawa T, Ueno Y. Pure Appl. Chem. 1996;68:711-714.
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(1996)
Pure Appl. Chem.
, vol.68
, pp. 711-714
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Toru, T.1
Watanabe, Y.2
Mase, N.3
Tsusaka, M.4
Hayakawa, T.5
Ueno, Y.6
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19
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0013541921
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note
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[7] Competitive hydrogen abstraction from the benzylic positions of Merrifield resin or polyether spacers of TentaGel might occur in the radical reactions on solid support, see: 3a
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20
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0013551698
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note
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[8] Merrifield resin (2-2.5 mmol/g, 200-400 mesh) from Acros organics was used in all of the experiments. All resins were pre-swelled in the reaction solvent before use.
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21
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0013515451
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note
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[9] Yield was based on the Cl content of Merrifield resin. The content of the vinyl moiety in the resin 2 was estimated to be 1.53 mmol/g.
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22
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2742528871
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[10] β-Bromoacetals were prepared according to the modified procedure reported in the literature, see: (a) Ueno Y, Chino K, Watanabe M, Moriya O, Okawara M. J. Am. Chem. Soc. 1982;104:5564-5566.
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(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 5564-5566
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Ueno, Y.1
Chino, K.2
Watanabe, M.3
Moriya, O.4
Okawara, M.5
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23
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37049068023
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(b) Ueno Y, Moriya O, Chino K, Watanabe M, Okawara M. J. Chem. Soc., Perkin Trans. 1 1986:1351-1356.
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(1986)
J. Chem. Soc., Perkin Trans. 1
, pp. 1351-1356
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Ueno, Y.1
Moriya, O.2
Chino, K.3
Watanabe, M.4
Okawara, M.5
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24
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0013480454
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The reactions have not been optimized for each substituent
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[11] The reactions have not been optimized for each substituent.
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25
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0013546709
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note
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1H nmr and ir spectra. The analysis of the substrate on resin was carried out by the ir spectrum.
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26
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0013510314
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note
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[13] Formation of neither 2-hexynal nor 2-hexynyl acetate was observed by tlc and gas chromatography after cleavage by Jones oxidation.
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27
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0000134099
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[14] Several procedures have been reported to achieve the effective separation of organotin species from the products. (a) Saigo K, Morikawa A, Mukaiyama T. Bull. Chem. Soc. Jpn. 1976;49:1656-1658.
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(1976)
Bull. Chem. Soc. Jpn.
, vol.49
, pp. 1656-1658
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Saigo, K.1
Morikawa, A.2
Mukaiyama, T.3
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33
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0037540307
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Organotin compounds on polymer supports have been reported. (f) Crosby NM, Wong GA. J. Org. Chem. 1975;40:1966-1971.
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(1975)
J. Org. Chem.
, vol.40
, pp. 1966-1971
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Crosby, N.M.1
Wong, G.A.2
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35
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0032565936
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(h) Dumartin G, Pourcel M, Delmond B, Donard O, Pereyre M. Tetrahedron Lett. 1998;39:4663-4666.
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(1998)
Tetrahedron Lett.
, vol.39
, pp. 4663-4666
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Dumartin, G.1
Pourcel, M.2
Delmond, B.3
Donard, O.4
Pereyre, M.5
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