-
7
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0025780257
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Chiral auxiliaries:
-
Chiral auxiliaries: Buschmann H., Scharf H.D., Hoffmann N., Esser P. Angew. Chem., Int. Ed. Engl. 30:1991;477
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Buschmann, H.1
Scharf, H.D.2
Hoffmann, N.3
Esser, P.4
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12
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0000663159
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Chiral ionic auxiliaries:
-
Chiral ionic auxiliaries: Gamlin J.N., Jones R., Leibovitch M., Patrick B., Scheffer J.R., Trotter J. Acc. Chem. Res. 29:1996;203
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Gamlin, J.N.1
Jones, R.2
Leibovitch, M.3
Patrick, B.4
Scheffer, J.R.5
Trotter, J.6
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15
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0001076630
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Pergamon: UK
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Szejtli, T. Cyclodextrin and their Inclusion Complexes Akademiai: Kiado, 1982. Szejtle, T. Comprehensive Supramolecular Chemistry; Pergamon: UK, 1996; Vol. 3, p 189???
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Comprehensive Supramolecular Chemistry
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16
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3142744911
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-
note
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We have employed some cage molecules as hosts, such as cyclodextrins (usually called 'cavity' though), zeolite, and Fujita's Pd-nanocage, which might be totally called 'supercage' molecules
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-
-
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31
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3142674563
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Diradical Borden W.T.
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Diradical Borden W.T.:1982;Wiley, New York
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(1982)
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39
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0004252595
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P.A. Grieco. London: Blackie Academic & Professional
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Grieco P.A. Organic Synthesis in Water. 1998;Blackie Academic & Professional, London
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(1998)
Organic Synthesis in Water
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41
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0034824575
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Quite recently, the asymmetric α-arylation of ketone enolates has been reported:
-
Quite recently, the asymmetric α-arylation of ketone enolates has been reported: Moradi W.A., Buchwald S.L. J. Am. Chem. Soc. 123:2001;7996
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J. Am. Chem. Soc.
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Moradi, W.A.1
Buchwald, S.L.2
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44
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0037163998
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Jorgensen M., Lee S., Liu X., Wolkowski J.P., Hartwig J.F. J. Am. Chem. Soc. 124:2002;12557
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Jorgensen, M.1
Lee, S.2
Liu, X.3
Wolkowski, J.P.4
Hartwig, J.F.5
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46
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0024840703
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Corey E.J., Jardine P.D., Virgil S., Yuen P.W., Connell R.D. J. Am. Chem. Soc. 111:1989;9243
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Corey, E.J.1
Jardine, P.D.2
Virgil, S.3
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Connell, R.D.5
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47
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84988141384
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Mangeney P., Tejero T., Alexakis A., Grosjean F., Normant J.F. Synthesis. 1988;255
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Synthesis
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Mangeney, P.1
Tejero, T.2
Alexakis, A.3
Grosjean, F.4
Normant, J.F.5
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48
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3142770089
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note
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3): 33% ee (R)
-
-
-
-
49
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0000826210
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For the equation to calculate the relative reactivity, see:
-
For the equation to calculate the relative reactivity, see: Wang Y.-F., Chen C.-S., Girdaukas G., Sih C.J. J. Am. Chem. Soc. 106:1984;3695
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Wang, Y.-F.1
Chen, C.-S.2
Girdaukas, G.3
Sih, C.J.4
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50
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33845557915
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Martin V.S., Woodard S.S., Katsuki T., Yamada Y., Ikeda M., Sharpless K.B. J. Am. Chem. Soc. 103:1981;6237
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Martin, V.S.1
Woodard, S.S.2
Katsuki, T.3
Yamada, Y.4
Ikeda, M.5
Sharpless, K.B.6
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52
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0037473571
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-
For strict hydrogen bonding with CDs bearing primary and secondary hydroxy groups, see:
-
For strict hydrogen bonding with CDs bearing primary and secondary hydroxy groups, see: Miyake K., Yasuda S., Harada A., Sumaoka J., Komiyama M., Shigekawa H. J. Am. Chem. Soc. 125:2003;50
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Miyake, K.1
Yasuda, S.2
Harada, A.3
Sumaoka, J.4
Komiyama, M.5
Shigekawa, H.6
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