Chemistry Reference
In-Depth Information
[14] G. L. Bolton, “Solid phase synthesis of azabicyclo[4.3.0]nonen-8-one amino acid
derivatives via intramolecular Pauson-Khand cyclization”
Tetrahedron Lett
. 1996,
37
(20), 3433-3436.
[15] A. R. Kennedy, W. J. Kerr, D. M. Lindsay, J. S. Scott, S. P. Watson, “Stereochemical
and mechanistic features of asymmetric Pauson-Khand processes”
Perk in 1
2000,
(24), 4366-4372.
[16] P. Areces, M. A. Duran, J. Plumet, M. B. Hursthouse, M. E. Light, “Synthe-
sis of Enantiopure 3-Azabicyclo[3.3.0]octen-7-one Derivatives via Intramolecular
Pauson-Khand Cycloaddition Reaction Using Tri-O-acetyl-D-glucal as Starting Ma-
terial”
J. Org. Chem.
2002,
67
(10), 3506-3509.
[17] P. Areces, E. Carrasco, J. Plumet, “From D-galactose to enantiopure 3-
azabicyclo[3.3.0]octen-7-one derivatives via Pauson-Khand reaction”
ARKIVOC
(Gainesville, FL, United States) 2005, (9), 165-174.
[18] B. Jiang, M. Xu, “Catalytic Diastereoselective Pauson-Khand Reaction: an Efficient
Route to Enantiopure Cyclopenta[c]proline Derivatives”
Org. Lett.
2002,
4
(23),
4077-4080.
[19] T. Ishikawa, H. Ishii, K. Shimizu, H. Nakao, J. Urano, T. Kudo, S. Saito, “Diastere-
oselective Total Synthesis of Isocarbacyclin from L-Ascorbic Acid”
J. Org. Chem.
2004,
69
(23), 8133-8135.
[20] N. Jeong, D. H. Kim, J. H. Choi, “Desymmetrization of meso-dienyne by asym-
metric Pauson-Khand type reaction catalysts”
Chem. Commun.
(Cambridge, United
Kingdom) 2004, (9), 1134-1135.
[21] R. M. Moriarty, N. Rani, L. A. Enache, M. S. Rao, H. Batra, L. Guo, R. A. Penmasta,
J. P. Staszewski, S. M. Tuladhar, O. Prakash, D. Crich, A. Hirtopeanu, R. Gilardi,
“The Intramolecular Asymmetric Pauson-Khand Cyclization as a Novel and General
Stereoselective Route to Benzindene Prostacyclins: Synthesis of UT-15 (Treprostinil)”
J. Org. Chem.
2004,
69
(6), 1890-1902.
[22] A. Lanver, H.-G. Schmalz, “A Pauson-Khand approach to new carbocyclic nucleoside
analogs”
Eur. J. Org. Chem.
2005, (7), 1444-1458.
[23] T. Honda, K. Kaneda, “Diastereoselective Formal Synthesis of a Monoterpene Alka-
loid, (-)-Incarvilline”
J. Org. Chem.
2007,
72
(17), 6541-6547.
[24] M. K. Pallerla, J. M. Fox, “Enantioselective Synthesis of (-)-Pentalenene”
Org. Lett.
2007,
9
(26), 5625-5628.
[25] P. Bremond, E. Girardeau, Y. Coquerel, J. Rodriguez, “Stereoselective synthesis of
the core of naturally occurring anti-HIV isolitseane B”
Lett. Org. Chem.
2007,
4
(4),
232-233.
[26] C. E. Madu, C. J. Lovely, “Steric promotion of the intramolecular Pauson-Khand
reaction of aryl enynes”
Synlett
2007, (13), 2011-2016.
[27] G. R. Dake, E. E. Fenster, B. O. Patrick, “A Synthetic Approach to the Fusicoc-
cane A-B Ring Fragment Based on a Pauson-Khand Cycloaddition/Norrish Type 1
Fragmentation”
J. Org. Chem.
2008,
73
(17), 6711-6715.
[28] X. Jia, R. M. Williams, “A diastereoselective intramolecular Pauson-Khand approach
to the construction of the BC-ring system in tuberostemoninol”
Tetrahedron: Asym-
metry
2008,
19
(24), 2901-2906.
[29] K. Kaneda, T. Honda, “Stereocontrolled synthesis of (
-skytanthine by means of
an intramolecular Pauson-Khand reaction”
Tetrahedron
2008,
64
(51), 11589-11593.
+
)-
