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3
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0028137098
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2. For recent preparations of the 3-aza-2-oxobicyclo[3.1.0]hexane ring system see: a) Chan, S.; Braish, T.F. Tetrahedron, 1994, 50, 9943-9950.
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6
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0024262556
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3. a) Ashton, W.T.; Meurer, L.C.; Cantone, C.L.; Field, A.K.; Hannah, J.; Karkas, J.D.; Liou, R.; Patel, G.F.; Perry, H.C.; Wagner, A.F.; Walton, E.; Tolman, R.L. J. Med. Chem., 1988, 31, 2304-2315.
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Ashton, W.T.1
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Karkas, J.D.6
Liou, R.7
Patel, G.F.8
Perry, H.C.9
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84949065308
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and references therein cited
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4. Burgess, K.; Ho, K-K.; Moye-Sherman, D. Synlett, 1994, 575-583, and references therein cited.
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Burgess, K.1
Ho, K.-K.2
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9
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0028912122
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5. For recent preparations of the 3-azabicyclo[3.1.0]hexane ring system see: a) Sagnard, I.; Sasaki, N.A.; Chiaroni, A.; Riche, C.; Potier, P. Tetrahedron Lett., 1995, 36, 3149-3152.
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Sagnard, I.1
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0000194469
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c) Watanuki, S.; Ochifuji, N.; Mori, M. Organometallics, 1995, 14, 5062-5067.
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0002872624
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Pearson, W.H. Ed.; JAI Press, Greenwich, CT
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6. For recent reviews, see: a) Boger, D.L. Advances in Heterocyclic Natural Products Synthesis; Pearson, W.H. Ed.; JAI Press, Greenwich, CT, 1992, vol 2, pp. 1-177.
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Boger, D.L.1
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0000841302
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7. Cardillo, B.; Galeazzi, R.; Mobbili, G.; Orena, M.; Rossetti, M. Heterocycles, 1994, 38, 2663-2676.
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17
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0024809070
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2O, which proceeds with moderate to low yields, see: Oumar-Mahamat, H.; Moustrou, C.; Surzur, J.-M.; Bertrand, M.-P. J. Org. Chem., 1989, 54, 5684-5688.
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Oumar-Mahamat, H.1
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Bertrand, M.-P.4
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18
-
-
0011977663
-
-
note
-
A and the phenyl group of the chiral auxiliary, in analogy with the results observed in the cyclisation of alkenyl amides (see Ref. 1b), although molecular mechanics calculations on the transition states were not carried out.
-
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-
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19
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0023275002
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10. a) Cardillo, G.; Orena, M.; Sandri, S.; Tomasini, C. Tetrahedron, 1987, 43, 2505-2512.
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Cardillo, G.1
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20
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0023574810
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b) Bongini, A.; Cardillo, G.; Orena, M.; Porzi, G.; Sandri, S. Tetrahedron, 1987, 43, 4377-4383.
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Bongini, A.1
Cardillo, G.2
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21
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0002325783
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c) Bongini, A.; Cardillo, G.; Orena, M.; Porzi, G.; Sandri, S. Chem. Lett., 1988, 87-90.
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22
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d) Bruni, E.; Cardillo, G.; Orena, M.; Sandri, S.; Tomasini, C. Tetrahedron Lett., 1989, 30, 1679-1682.
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e) Orena, M.; Porzi, G.; Sandri, S. J. Chem. Res., (S), 1990, 376; (M), 1990, 2701-2711.
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0011989138
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g) Cardillo, G.; Orena, M.; Penna, M.; Sandri, S.; Tomasini, C. Tetrahedron, 1991, 47, 2263-2272.
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h) Orena, M.; Porzi, G.; Sandri, S. J. Org. Chem., 1992, 57, 6532-6536.
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i) Orena, M.; Porzi, G.; Sandri, S. J. Chem. Res., (S), 1993, 318-319; (M), 1993, 2125-2152.
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0011922973
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i) Orena, M.; Porzi, G.; Sandri, S. J. Chem. Res., (S), 1993, 318-319; (M), 1993, 2125-2152.
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30
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3042988525
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and subsequent versions, e.g. MM2-87, MM2-89, MM2-91
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11. The MM+ force field is an extension of MM2 which was developed by Allinger and co-workers. As references see: a) Allinger, N.L. J. Am. Chem. Soc., 1977, 99, 8127-8134, and subsequent versions, e.g. MM2-87, MM2-89, MM2-91.
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Allinger, N.L.1
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0012880986
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Quantum chemistry program exchange. Bloomington, Indiana, program #395, molecular mechanics
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Burkert, U.; Allinger, N.L. edd., American Chemical Society, Washington, D.C.
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b) Allinger, N.L.; Yuh, Y.H. Quantum Chemistry Program Exchange. Bloomington, Indiana, Program #395, Molecular Mechanics, Burkert, U.; Allinger, N.L. edd., ACS Monograph 177, American Chemical Society, Washington, D.C., 1982.
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84988072785
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Flurchick, K.M.6
Teeter, M.M.7
-
33
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0011951749
-
-
Feb. The program is enclosed in Hyperchem package, release 4.0, available from Hypercube, Waterloo, Canada
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d) Lipkowitz, K.B., QCPE Bulletin, Indiana University, 12, 1 (Feb. 1982). The program is enclosed in Hyperchem package, release 4.0, available from Hypercube, Waterloo, Canada.
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-
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Lipkowitz, K.B.1
-
34
-
-
0011919446
-
-
note
-
AB = 10.3), 4.03 (dd, B portion of an ABX system, 1H, J = 11.7, J = 6.4), 4.64 (dd, X portion of an ABX system, 1H, OH, J = 6.4, J = 4.8), 5.15 (q, 1H, J = 7.2), 7.12 - 7.42 (m, 5 ArH).
-
-
-
-
35
-
-
0021757436
-
-
13. Weiner, S.J.; Kollman, P.A.; Case, D.A.; Singh, V.C.; Ghio, C.; Alagona, G.; Profeta, S.; Weiner, P. J. Am. Chem. Soc., 1984, 106, 765-784.
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Weiner, S.J.1
Kollman, P.A.2
Case, D.A.3
Singh, V.C.4
Ghio, C.5
Alagona, G.6
Profeta, S.7
Weiner, P.8
-
36
-
-
11944251068
-
-
14. The few lacking bending parameters were calculated according to: a) Halgren, T. J. Am. Chem. Soc., 1990, 112, 4710-4723.
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Halgren, T.1
-
37
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-
0029011701
-
-
b) Cornell, W.D.; Cieplak, P.; Bayly, C.I.; Gould, J.R.; Merz, K.M.; Ferguson, D.M.; Spellmeyer, D.C.; Fox, T.; Caldwell, J.W.; Kollman, P.A. J.Am. Chem. Soc., 1995, 117, 117, 5179-5197.
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Cornell, W.D.1
Cieplak, P.2
Bayly, C.I.3
Gould, J.R.4
Merz, K.M.5
Ferguson, D.M.6
Spellmeyer, D.C.7
Fox, T.8
Caldwell, J.W.9
Kollman, P.A.10
-
38
-
-
0011919571
-
-
note
-
B), 3.71 (dd, 1H, J = 6.8, J = 11.1), 3.92 (dd, 1H, J = 4.2, J = 11.1), 4.79 (m, 2H), 5.50 (q, 1H, J = 7.2), 7.18 - 7.41 (m, 5 ArH).
-
-
-
-
39
-
-
0015520853
-
-
16. Shioiri, T.; Ninomiya, K.; Yamada, S. J. Am. Chem. Soc., 1972, 94, 6203-6205.
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Shioiri, T.1
Ninomiya, K.2
Yamada, S.3
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