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1. For natural fused polycyclic ethers, see: (a) Shimizu, Y. Chem. Rev. 1993, 93, 1685.
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Shimizu, Y.1
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3. Endo selective activation by π-donor: (a) Nicolaou, K. C.; Prasad, C. V. C.; Somers, P. K.; Hwang, C.-K. J. Am. Chem. Soc. 1989, 111, 5330.
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(b) Mukai, C.; Sugimoto, Y.; Ikeda, Y.; Hanaoka, M. Tetrahedron Lett. 1994, 35, 2183.
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Mukai, C.1
Sugimoto, Y.2
Ikeda, Y.3
Hanaoka, M.4
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7
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0029814752
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Intramolecular Nicolas Reaction
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(d) Mori, Y.; Yaegashi, K.; Furukawa, H. J. Am. Chem. Soc. 1996, 118, 8158. Intramolecular Nicolas Reaction:
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Mori, Y.1
Yaegashi, K.2
Furukawa, H.3
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0028216189
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Palladium-catalyzed cyclization
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(e) Mukai, C.; Ikeda, Y.; Sugimoto, Y.; Hanaoka, M. Tetrahedron Lett. 1994, 35, 2179. Palladium-catalyzed cyclization:
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Tetrahedron Lett.
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Mukai, C.1
Ikeda, Y.2
Sugimoto, Y.3
Hanaoka, M.4
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0025289014
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Antibody-catalyzed cyclization
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(g) Suzuki, T.; Sato, O.; Hirama, M. ibid. 1990, 31, 4747. Antibody-catalyzed cyclization:
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Tetrahedron Lett.
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Suzuki, T.1
Sato, O.2
Hirama, M.3
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0027922048
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(h) Janda, K.; Shevlin, C. G.; Lerner, R. A. Science 1993, 259, 490.
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Science
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Lerner, R.A.3
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4. Fujiwara, K.; Tokiwano, T.; Murai, A. Tetrahedeon Lett. 1995, 36, 8063.
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Fujiwara, K.1
Tokiwano, T.2
Murai, A.3
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13
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33845185491
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5. Endo selective activation by π-donor: (a) Nicolaou, K. C.; Prasad, C. V. C.; Somers, P. K.; Hwang, C.-K. J. Am. Chem. Soc. 1989, 111, 5335.
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Nicolaou, K.C.1
Prasad, C.V.C.2
Somers, P.K.3
Hwang, C.-K.4
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14
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0010721330
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Antibody-catalyzed cyclization
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(b) Matsukura, H.; Morimoto, M.; Kosino, H.; Nakata, T. Tetrahedron Lett. 1997, 55, 488. Antibody-catalyzed cyclization:
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Matsukura, H.1
Morimoto, M.2
Kosino, H.3
Nakata, T.4
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0028913329
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(c) Janda, K.; Shevlin, C. G.; Lerner, R. A. J. Am. Chem. Soc. 1995, 117, 2659. See also
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Janda, K.1
Shevlin, C.G.2
Lerner, R.A.3
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17
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0001293261
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(e) Nicolaou, K. C.; Claremon, D. A.; Barnelte, W. E. J. ibid. 1980, 102, 6611.
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Nicolaou, K.C.1
Claremon, D.A.2
Barnelte, W.E.J.3
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19
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0024340606
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(g) Kocienski, P. J.; Love, C. J.; Whitby, R. J.; Costello, G.; Roberts, D. A. Tetrahedron 1989, 45, 3839.
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Kocienski, P.J.1
Love, C.J.2
Whitby, R.J.3
Costello, G.4
Roberts, D.A.5
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15844395902
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(h) Sasaki, M.; Inoue, M.; Tachibana, K. J. Org. Chem. 1994, 59, 715.
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Sasaki, M.1
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Tachibana, K.3
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21
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33845378115
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6. Lewis acid-catalyzed intermolecular nucleophilic reactions at C3 position in 2, 3-epoxy-1-ol system have been reported, (a) Caron, M.; Sharpless, K. B. J. Org. Chem. 1985, 50, 1557.
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Caron, M.1
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24
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0010667523
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(d) Gao, L.-x.; Saitoh, H.; Feng, F.; Murai, A. ibid. 1991, 1787,
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Gao, L.-X.1
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25
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0001008984
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3, see: Forsberg, J. H.; Spasiano, V. T.; Balasubramanian, T. M.; Liu, G. K.; Kinsley, S. A.; Duckworth, C. A.; Poteruca, J. J.; Brown, P. S.; Miller, J. L. J. Org. Chem. 1987, 52, 1017.
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Forsberg, J.H.1
Spasiano, V.T.2
Balasubramanian, T.M.3
Liu, G.K.4
Kinsley, S.A.5
Duckworth, C.A.6
Poteruca, J.J.7
Brown, P.S.8
Miller, J.L.9
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26
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84945959007
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2O were observed in other lanthanoid catalyst systems: (a) Sasai, H.; Suzuki, T.; Arai, S.; Arai, T.; Shibasaki, M. J. Am. Chem. Soc. 1992, 114, 4418.
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J. Am. Chem. Soc.
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Sasai, H.1
Suzuki, T.2
Arai, S.3
Arai, T.4
Shibasaki, M.5
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28
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0010721331
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note
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3 did not effect in yield and selectivity.
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