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b) Paquette, L.A. in: Studies in Natural Products Chemistry, Vol. 11 (Part G), Ed. Atta-ur-Rahman, Elsevier Science Publishers, N.Y., 1992, p. 3-69;
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Paquette, L.A.1
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c) Swindell, C.S. in: Studies in Natural Products Chemistry, Vol. 12 (Part H), Ed. Atta-ur-Rahman, Elsevier Science Publishers, N.Y., 1993, p. 179-231;
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d) Nicolaou, K.C.; Dai, W.M.; Guy, R.K. Angew. Chem. Int. Ed. Eng. 1994, 33, 15-44;
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e) Boa, A.N.; Jenkins, P.R.; Lawrence, N.J. Contemporary Organic Synthesis 1994, 1, 47-75;
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Boa, A.N.1
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see also: f) Nicolaou, K.C.; Yang, Z.; Liu, J.-J.; Ueno, H.; Nantermet, P.G.; Guy, R.K.; Claiborne, C.F.; Renaud, J.; Couladouros, E.A.; Paulvannan, K.; Sorensen, E.J. Nature 1994, 367, 630-634;
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Nicolaou, K.C.1
Yang, Z.2
Liu, J.-J.3
Ueno, H.4
Nantermet, P.G.5
Guy, R.K.6
Claiborne, C.F.7
Renaud, J.8
Couladouros, E.A.9
Paulvannan, K.10
Sorensen, E.J.11
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g) Danishefsky, S.J.; Masters, J.J.; Joung, W.B.; Link, J.T.; Snyder, L.B.; Magee, T.V.; Jung, D.K.; Isaacs, R.C.A.; Bornmann, W.G.; Alaimo, C.A.; Coburn, C.A.; DiGrandi, M.J. J. Am. Chem. Soc. 1996, 118, 2843-2859
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Magee, T.V.6
Jung, D.K.7
Isaacs, R.C.A.8
Bornmann, W.G.9
Alaimo, C.A.10
Coburn, C.A.11
DiGrandi, M.J.12
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b) Berkowitz, W.F.; Peruma Hal, J.; Amarasekara, A. Tetrahedron Lett. 1985, 26, 3665-3668;
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Berkowitz, W.F.1
Peruma Hal, J.2
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c) Swindell, C.S.; Patel, B.P.; deSolms, S.J.; Springer, J.P. J. Org. Chem. 1987, 52, 2346-2355;
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e) Benchikh Le Hocine, M.; Khac, D.D.; Fetizon, M. Synth. Commun. 1992, 22, 245-255;
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f) Blechert, S.; Muller, R.; Beitzel, M. Tetrahedron 1992, 48, 6953-6964;
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g) Winkler, J.D.; Subrahmanyam, D.; Hsung, R.P. Tetrahedron 1993, 49, 291; ibid, 1992, 48, 7049-7056;
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g) Winkler, J.D.; Subrahmanyam, D.; Hsung, R.P. Tetrahedron 1993, 49, 291; ibid, 1992, 48, 7049-7056;
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a) Holton, R.A.; Kim, H.-B.; Somoza, C.; Liang, F.; Biediger, R.J.; Boatman, P.D.; Shindo, M.; Smith, C.C.; Kim, S.; Nadizadeh, H.; Suzuki, Y.; Tao, C.; Vu, P.; Gentile, L.N.; Liu, J.H. J. Am. Chem. Soc. 1994, 116, 1599-1600;
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0342866778
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ref. 1b
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Prepared form (lR)-(+)-camphor: Paquette, L.A.; Huber, S.K.; Thompson, R.C. J. Org. Chem. 1993, 58, 6874-6882
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25
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0343301855
-
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note
-
The stereochemistry at C-10 in 2 (camphor numbering) was deduced from NOE experiment on 3; the tertiary hydroxyl group at C-2 was tentatively assigned as exo, according to the known stereochemical course of the additions of organometallics to camphor and its derivatives.
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26
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37049079386
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Grigg, R.; Scott, R.; Stevenson, P. J. Chem. Soc. Perkin Trans, 1, 1988, 1357-1364
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27
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85063243013
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13 C, HMQC, HMBC , IR, MS and microanalyses) are fully consistent with proposed structures
-
13 C, HMQC, HMBC , IR, MS and microanalyses) are fully consistent with proposed structures.
-
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28
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37049072660
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