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References
[1] H. W. Sternberg, H. Greenfield, R. A. Friedel, J. Wotiz, R. Markby, and I. Wender,
A new type of of metallo-organic complex derived from dicobalt octacarbonyl and
acetylenes,
J. Am. Chem. Soc.
,
76
, 1457-1458 (1954).
[2] I. U. Khand, G. R. Knox, P. L. Pauson, and W. E. Watts, M. I. Foremann Reaction of
acetylenehexacarbonyldicobalt complexes, (R
1
C
2
R
2
)Co
2
(CO)
6
, with norbornene and
its derivatives,
J. Chem. Soc., Perkin Trans. 1
, 977-981 (1973).
[3] C. Exon and P. Magnus, Stereoselectivity of intramolecular dicobalt octacarbonyl
alkene-alkyne cyclizations: short synthesis of
dl
-coriolin,
J. Am. Chem. Soc
.,
105
,
2477-2478 (1983).
[4] P. Magnus and L. M. Principe, Origins of 1,2- and 1,3-stereoselectivity in di-
cobaltoctacarbonyl alkene-alkyne cyclizations for the synthesis of substituted bicy-
clo[3.3.0]octenones,
Tetrahedron Lett.
,
26
, 4851-4854 (1985).
[5] V. Rautenstrauch, P. Megard, J. Conesa, and W. Kuster, 2-Pentylcyclopent-2-en-1-
one by catalytic Pauson-Khand reaction,
Angew. Chem. Int. Ed. Engl
.,
29
, 1413-1416
(1990).
[6] N. Iwasawa, A novel rearrangement of 1-alkynylcyclopropanol to 2-cyclopenten-1-
one via dicobalt hexacarbonyl complex,
Chem. Lett.
, 21, 473-476 (1992).
[7] N. Iwasawa and T. Matsuo, Rearrangement of 1-alkynylcyclopropanol to 3-
substituted 2-cyclopentenone promoted by a catalytic amount of octacarbonyldicobalt-
triphenylphosphite,
Chem. Lett.
,
22
, 997-1000 (1993).
[8] N. Iwasawa, T. Matsuo, M. Iwamoto, and T. Ikeno, Rearrangement of 1-(1-
alkynyl)cyclopropanols to 2-cyclopentenones via their hexacarbonyldicobalt com-
plexes. A new use of alkyne
Co
2
(CO)
6
complexes in organic synthesis,
J. Am. Chem.
Soc
.,
120
, 3903-3914 (1998).
[9] N. Jeong, S. H. Hwang, Y. Lee, and Y. K. Chung, Catalytic version of the intramolecular
Pauson-Khand reaction,
J. Am. Chem. Soc.
,
116
, 3159-3160 (1994).
[10] A. C. Comely, S. E. Gibson, A. Stevenazzi, and N. J. Hales, New stable catalysts of
the Pauson-Khand annelation,
Tetrahedron Lett.
,
42
, 1183-1185 (2001).
[11] S. E. Gibson, C. Johnstone, and A. Stevenazzi, A stable catalyst of the Pauson-Khand
annelation,
Tetrahedron
,
58
, 4937-4942 (2002).
[12] M. Hayashi, Y. Hashimoto, Y. Yamamoto, J. Usuki, and K. Saigo, Phosphane
sulfide/octacarbonyldicobalt-catalyzed Pauson-Khand reaction under an atmospheric
pressure of carbon monoxide,
Angew. Chem., Int. Ed.
,
39
, 631-633 (2000).
[13] Y. Tang, L. Deng, Y. Zhang, G. Dong, J. Chen, and Z. Yang, Tetramethyl
thiourea/Co
2
(CO)
8
-catalyzed Pauson-Khand reaction under balloon pressure of CO,
Org. Lett.
,
7
, 593-595 (2005).
[14] T. Sugihara and M. Yamaguchi, The catalytic Pauson-Khand reaction promoted by a
small amount of 1,2-dimethoxyethane or water,
Synlett
, 1384-1386 (1998).
[15] J. Blanco-Urgoiti, L. Casarrubios, G. Domınguez, and J. Perez-Castells, New protocol
for the catalytic Pauson-Khand reaction induced by molecular sieves,
Tetrahedron
Lett.
,
43
, 5763-5765 (2002).
[16] B. Y. Lee, Y. K. Chung, N. Jeong, Y. Lee, and S. H. Hwang, (Indenyl)cobalt(I)-
catalyzed cocyclization of alkyne, alkene, and carbon monoxide to cyclopentenones,
J. Am. Chem. Soc.
,
116
, 8793-8794 (1994).
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