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0000635013
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Spring-er, Berlin
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(a) Comprehensive Asymmetric Catalysis, Vol. 1-3, (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Spring-er, Berlin, 1999;
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Comprehensive Asymmetric Catalysis
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Jacobsen, E.N.1
Pfaltz, A.2
Yamamoto, H.3
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7
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0003797080
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(g) Asymmetric Catalysis, (Ed.: B. Bosnich), Martinus Nijhoff Publishers, Dordrecht, 1986.
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Asymmetric Catalysis
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Bosnich, B.1
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8
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33748983103
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D. J. Berrisford, C. Bolm, K. B., Sharpless, Angew. Chem., Int. Ed. Engl. 1995, 34, 1059-1070.
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Berrisford, D.J.1
Bolm, C.2
Sharpless, K.B.3
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10
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0003091922
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(a) BPBP [2,2′-bis(diphenylphosphanyl)-1,1′-biphenyl] was also named for this bisphosphine ligand but was not successfully synthesized. The monophosphine (5-phenyldibenzophosphole) was obtained instead of BPBP: A. Uehara, J. C. Bailar Jr., J. Organomet. Chem. 1982, 239, 1-10;
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(1982)
J. Organomet. Chem.
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Uehara, A.1
Bailar Jr., J.C.2
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11
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45249127192
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see also preliminary communication: T. K. Miyamoto, Y. Matsuura, K. Okude, H. Ichida, Y. Sasaki, J. Organomet. Chem. 1989, 373, C8-C12;
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J. Organomet. Chem.
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Miyamoto, T.K.1
Matsuura, Y.2
Okude, K.3
Ichida, H.4
Sasaki, Y.5
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12
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0023312386
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(b) M. A. Bennett, S. K. Bhargava, K. D. Griffiths, G. B. Robertson, Angew. Chem. Int. Ed. Engl. 1987, 26, 260-261;
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Angew. Chem. Int. Ed. Engl.
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Bennett, M.A.1
Bhargava, S.K.2
Griffiths, K.D.3
Robertson, G.B.4
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14
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0030021640
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(d) The activation barrier to axiual torsion in selectively deuterated BIPHEP was determined as only 22±1 kcal/mol, suggesting axial rotation at room temperature or above: O. Desponds, M. Schlosser, Tetrahedron Lett. 1996, 37, 47-48;
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(1996)
Tetrahedron Lett.
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Desponds, O.1
Schlosser, M.2
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15
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0033733961
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(e) M. Ogasawara, K. Yoshida, T. Hayashi, Organometallics 2000, 19, 1567-1571;
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Organometallics
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Ogasawara, M.1
Yoshida, K.2
Hayashi, T.3
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16
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0034300043
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(f) M. D. Tudor, J. J. Becker, P. S. White, M. R., Gangé Organometallics, 2000, 19, 4376-4384.
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Organometallics
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Tudor, M.D.1
Becker, J.J.2
White, P.S.3
Gangé, M.R.4
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17
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0000171979
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BIPHEP was named after 6,6′-substituted MeO-BIPHEP. (a) R. Schmid, E. A. Broger, M. Cereghetti, Y. Crameri, J. Foricher, M. Lalonde, R. K. Müller, M. Scalone, G. Schoettel, U. Zutter, Pure Appl. Chem. 1996, 68, 131-138; (b) G. Trabesinger, A. Albinati, N. Feiken, R. W. Kunz, P. S. Pregosin, M. Tschoerner, J. Am. Chem. Soc., 1997, 119, 6315-6323, and references cited therein.
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(1996)
Pure Appl. Chem.
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Schmid, R.1
Broger, E.A.2
Cereghetti, M.3
Crameri, Y.4
Foricher, J.5
Lalonde, M.6
Müller, R.K.7
Scalone, M.8
Schoettel, G.9
Zutter, U.10
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18
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0030839003
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and references cited therein
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BIPHEP was named after 6,6′-substituted MeO-BIPHEP. (a) R. Schmid, E. A. Broger, M. Cereghetti, Y. Crameri, J. Foricher, M. Lalonde, R. K. Müller, M. Scalone, G. Schoettel, U. Zutter, Pure Appl. Chem. 1996, 68, 131-138; (b) G. Trabesinger, A. Albinati, N. Feiken, R. W. Kunz, P. S. Pregosin, M. Tschoerner, J. Am. Chem. Soc., 1997, 119, 6315-6323, and references cited therein.
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J. Am. Chem. Soc.
, vol.119
, pp. 6315-6323
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Trabesinger, G.1
Albinati, A.2
Feiken, N.3
Kunz, R.W.4
Pregosin, P.S.5
Tschoerner, M.6
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19
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0033558168
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(a) K. Mikami, T. Korenaga, M. Terada, T. Ohkuma, T. Pham, R. Noyori, Angew. Chem. Int. Ed. 1999, 38, 495-497;
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Angew. Chem. Int. Ed.
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Mikami, K.1
Korenaga, T.2
Terada, M.3
Ohkuma, T.4
Pham, T.5
Noyori, R.6
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20
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0034675555
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(b) For a review of "asymmetric activation", see: K. Mikami, M. Terada, T. Korenaga, Y. Matsumoto, M. Ueki, R., Angelaud, Angew. Chem. Int. Ed. 2000, 39, 3532-3556.
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(2000)
Angew. Chem. Int. Ed.
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Mikami, K.1
Terada, M.2
Korenaga, T.3
Matsumoto, Y.4
Ueki, M.5
Angelaud, R.6
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21
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85037274800
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Ph.D. Thesis, Tokyo Institue of Technology
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-3 kJ/mol K). However, the epimerization was not observed between both diastereomeric complexes at -35°C, presumably because the temperature was too low for isomerization of BIPHEP ligand.
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(2000)
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Korenaga, T.1
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22
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85037286787
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note
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2).
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23
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85037285307
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note
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2).
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24
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0003662632
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Gaussian, Inc., Pittsburgh PA
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M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, V. G. Zakrzewski, J. A. Montgomery, Jr., R. E. Stratmann, J. C. Durant, S. Dapprich, J. M. Millam, A. D. Daniels, K. N. Kudin, M. C. Strain, O. Farkas, J. Tomasi, V. Barone, M. Cossi, R. Cammi, B. Mennucci, C. Pomelli, C. Adamo, S. Clifford, J. Ochterski, G. A. Petersson, P. Y. Ayala, Q. Cui, K. Morokuma, D. K. Malick, A. D. Rabuck, K. Raghavachari, J. B. Foresman, J. Cioslowski, J. V. Ortiz, A. G. Baboul, B. B. Stefanov, G. Lin, A. Liashenko, P. Piskorz, I. Komaromi, R. Gomperts, R. L. Martin, D. J. Fox, T. Keith, M. A. Al-Laham, C. Y. Peng, A. Nanayakkara, C. Gonzalez, M. Challacombe, P. M. W. Gill, B. Johnson, W. Chen, M. W. Wong, J. L. Andres, C. Gonzalez, M. Head-Gordon, E. S. Replogle, J. A. Pople, Gaussian 98, Revision A. 7, Gaussian, Inc., Pittsburgh PA, 1998.
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Gaussian 98, Revision A. 7
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Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
Zakrzewski, V.G.7
Montgomery Jr., J.A.8
Stratmann, R.E.9
Durant, J.C.10
Dapprich, S.11
Millam, J.M.12
Daniels, A.D.13
Kudin, K.N.14
Strain, M.C.15
Farkas, O.16
Tomasi, J.17
Barone, V.18
Cossi, M.19
Cammi, R.20
Mennucci, B.21
Pomelli, C.22
Adamo, C.23
Clifford, S.24
Ochterski, J.25
Petersson, G.A.26
Ayala, P.Y.27
Cui, Q.28
Morokuma, K.29
Malick, D.K.30
Rabuck, A.D.31
Raghavachari, K.32
Foresman, J.B.33
Cioslowski, J.34
Ortiz, J.V.35
Baboul, A.G.36
Stefanov, B.B.37
Lin, G.38
Liashenko, A.39
Piskorz, P.40
Komaromi, I.41
Gomperts, R.42
Martin, R.L.43
Fox, D.J.44
Keith, T.45
Al-Laham, M.A.46
Peng, C.Y.47
Nanayakkara, A.48
Gonzalez, C.49
Challacombe, M.50
Gill, P.M.W.51
Johnson, B.52
Chen, W.53
Wong, M.W.54
Andres, J.L.55
Gonzalez, C.56
Head-Gordon, M.57
Replogle, E.S.58
Pople, J.A.59
more..
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25
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85037270695
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note
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All the calculations were done by using Gaussian 98 program on the SGI Origin 2000 computer at the Computer Center of Tokyo Institute of Technology.
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26
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85037276193
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note
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2 groups, are quite small.
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27
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0345904863
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Oki has reported that free energies of activation of more than ca. 23 kcal/mol separate the atropisomers: Top. Stereochem. 1983, 14, 1-81.
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(1983)
Top. Stereochem.
, vol.14
, pp. 1-81
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28
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85037273579
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note
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[6a]).
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29
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33847087228
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(a) G. Bott, L. D. Field, S. Sternhell, J. Am. Chem. Soc. 1980, 102, 5618-5626;
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J. Am. Chem. Soc.
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Bott, G.1
Field, L.D.2
Sternhell, S.3
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30
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0346535900
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(b) C. Rousel, A. Liden, M. Chanon, J. Metzger, J. Sandstrom, J. Am. Chem. Soc. 1976, 98, 2487-2852;
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J. Am. Chem. Soc.
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Rousel, C.1
Liden, A.2
Chanon, M.3
Metzger, J.4
Sandstrom, J.5
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31
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0000364123
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(c) B. Nilsson, P. Martinson, K. Olsson, R. E. Carter, J. Am. Chem. Soc., 1974, 96, 3190-3197.
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J. Am. Chem. Soc.
, vol.96
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Nilsson, B.1
Martinson, P.2
Olsson, K.3
Carter, R.E.4
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32
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85037268424
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note
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[15a]).
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