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References
[1] P. Magnus, D. P. Becker, “Stereospecific Dicobalt Octacarbonyl Mediated Enyne
Cyclization for the Enantiospecific Synthesis of a 6a-Carbocycline Analog”
J. Am.
Chem. Soc.
1987,
109
(24), 7495-7498.
[2] P. Magnus, L. M. Principe, J. M. Slater, “Stereospecific Dicobalt Octacarbonyl Me-
diated Enyne Cyclization for the Synthesis of the Cytotoxic Sesquiterpene (
+
/-)-
Quadrone”
J.Org. Chem.
1987,
52
(8), 1483-1486.
[3] J. Mulzer, K. D. Graske, B. Kirste, “Asymmetric synthesis of carbacyclin precursors
by Pauson-Khand cyclization”
Liebigs Ann. Chem.
1988, (9), 891-897.
[4] W. R. Roush, J. C. Park, “Asymmetric Allylborations of 3-Decynal Dicobalt Hex-
acarbonyl - Cobalt Induced Reversal of Enantioselectivity and Applications to Highly
Diastereoselective Intramolecular Pauson-Khand Reactions”
Tetrahedron Lett
. 1991,
32
(44), 6285-6288.
[5] S. Takano, S, K. Inomata, K. Ogasawara, “A New Enantiospecific Route to (-)-Kainic
Acid Via the Intramolecular Pauson-Khand Reaction”
Chem. Commun.
1992, (2),
169-170.
[6] (a) S. E. Yoo, S. H. Lee, N. Jeong, I. Cho, “A Total Synthesis of (-)-Alpha-Kainic
Acid by the Pauson-Khand Reaction”
Tetrahedron Lett
. 1993,
34
(21), 3435-3438;
(b) S. E. Yoo, S. H. Lee, “A Total Synthesis of (-)-Alpha-Kainic Acid Involving a
Pauson-Khand Reaction as the Key Step”
J. Org. Chem
. 1994,
59
(23), 6968-6972.
[7] M. E. Kraft, R. A. Holton, “Preparation of a New, Highly Reactive Form of Iron(0)
and Its Use in Deprotonation of Carbonyl-Compounds”
J. Org. Chem.
1984,
49
(19),
3669-3670.
[8] W. E. Lindsell, P. N. Preston, A. B. Rettie, “ Synthesis and Characterization of
Hexacarbonyldicobalt Complexes Derived from 2-Propynyl and 3-Butynyl 4,6-Di-O-
Acetyl-2,3-Dideoxy-Alpha-D-Erythro-Hex-2-Enopyranosides”
Carbohyd. Res.
1994,
254
, 311-316.
[9] J. Marcocontelles, “The Pauson-Khand Reaction on Carbohydrate Templates .1.
Synthesis of Bis-Heteroannulated Pyranosides”
Tetrahedron Lett
. 1994,
35
(28),
5059-5062.
[10] J. MarcoContelles, “Asymmetric Pauson-Khand reaction. Cobalt-mediated cycloiso-
merization of 1,6-enynes in carbohydrate templates: Synthesis of bis-heteroannulated
pyranosides”
J. Org. Chem.
1996,
61
(22), 7666-7670.
[11] (a) N. Naz, T. H. Altel, Y. Alabed, W. Voelter, “Synthesis of Polyfunctionalized Bis-
Annulated Pyranosides - Useful Intermediates for Triquinane Synthesis”
Tetrahedron
Lett
. 1994,
35
(46), 8581-8582; (b) N. Naz, T. H. AlTel, Y. Alabed, W. Voelter,
R. Ficker, W. Hiller, “Palladium-cobalt-mediated double annulation process: A new
strategy to chiral and polysubstituted bis-cyclopentanoids on carbohydrate precursors”
J. Org. Chem
. 1996,
61
(10), 3250-3255.
[12] C. Mukai, M. Uchiyama, S. Sakamoto, M. Hanaoka, “A highly diastereoselective
construction of optically active bicyclo[3.3.0]octenone derivatives from L-ascorbic
acid via Pauson-Khand reaction”
Tetrahedron Lett
. 1995,
36
(32), 5761-4.
[13] B. Alcaide, C. Polanco, M. A. Sierra, “Synthesis of fused tricyclic beta-lactams by the
Pauson-Khand cyclization of enyne-2-azetidinones”
Tetrahedron Lett
. 1996,
37
(38),
6901-6904.
