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19
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85038544397
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note
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1H NMR spectroscopy, looking at the protons of the propargyl (triplet at δ=2.39 and doublet at 3.85 ppm) and the allenyl (doublet at δ=5.16 and triplet at 6.34 ppm) group.
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20
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0001406943
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85038543431
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note
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[13] Crystallographic data (excluding structure factors) for 7a has been deposited with the Cambridge Crystallographic Data Centre.
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23
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0001992172
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[14] K. L. Habermas, S. E. Denmark, Org. React. 1994, 45, 1-158. S. E. Denmark, In Comprehensive Organic Synthesis; B. M. Trost, I. Fleming, eds.; Pergamon: Oxford, 1991; Vol. 5, pp. 751-784.
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Habermas, K.L.1
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0000646877
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[14] K. L. Habermas, S. E. Denmark, Org. React. 1994, 45, 1-158. S. E. Denmark, In Comprehensive Organic Synthesis; B. M. Trost, I. Fleming, eds.; Pergamon: Oxford, 1991; Vol. 5, pp. 751-784.
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Denmark, S.E.1
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25
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0029003734
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[15] Prepared by Pauson-Khand reactions. But at least one additional substituent is necessary. M. Ahmar, F. Antrax, B. Cazes, Tetrahedron Lett. 1995, 36, 4417-4420. M. Ahmar, O. Chabanis, J. Gauthier, B. Cazes, Tetrahedron Lett. 1997, 38, 5277-5280. M. Ahmar, C. Locatelli, D. Colombier, B. Cazes, Tetrahedron Lett. 1997, 38, 5281-5284.
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Ahmar, M.1
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26
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0030857707
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[15] Prepared by Pauson-Khand reactions. But at least one additional substituent is necessary. M. Ahmar, F. Antrax, B. Cazes, Tetrahedron Lett. 1995, 36, 4417-4420. M. Ahmar, O. Chabanis, J. Gauthier, B. Cazes, Tetrahedron Lett. 1997, 38, 5277-5280. M. Ahmar, C. Locatelli, D. Colombier, B. Cazes, Tetrahedron Lett. 1997, 38, 5281-5284.
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Ahmar, M.1
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Cazes, B.4
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27
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0030805614
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[15] Prepared by Pauson-Khand reactions. But at least one additional substituent is necessary. M. Ahmar, F. Antrax, B. Cazes, Tetrahedron Lett. 1995, 36, 4417-4420. M. Ahmar, O. Chabanis, J. Gauthier, B. Cazes, Tetrahedron Lett. 1997, 38, 5277-5280. M. Ahmar, C. Locatelli, D. Colombier, B. Cazes, Tetrahedron Lett. 1997, 38, 5281-5284.
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Ahmar, M.1
Locatelli, C.2
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