Chemistry Reference
In-Depth Information
[58] (a) Ichikawa, M., Takahashi, M., Aoyagi, S. and Kibayashi, C. (2004) Total synthesis
of (
)-incarvillateine.
J. Am. Chem. Soc.
,
126
,
16553-16558; (b) Ichikawa, M., Aoyagi, S. and Kibayashi, C. (2005) Total synthesis
of (-)-incarvalline.
Tetrahedron Lett.
,
46
, 2327-2329; (c) Hong, B.-C., Gupta, A.
K., Wu, M.-F., Liao, J.-H. and Lee, G.-H. (2003) Hetero [6
−
)-incarvilline, (
+
)-incarvine C, and (
−
3] cycloaddition of
fulvenes with
N
-alkylidene glycine esters: a facile synthesis of the delavayine and
incarvillateine framework.
Org. Lett.
,
5
, 1689-1692.
[59] Sugihara, T., Yamaguchi, M. and Nishizawa, M. (1999) Activation of alkyne-dicobalt
hexacarbonyl complexes by the Lewis bases a new trend of the Pauson-Khand reaction.
J. Synth. Org. Chem. Jpn.
,
57
, 158-169.
[60] Jiao, L., Zhou, L.-G. and Yu, Z.-X. (2010) Rh(I)-catalyzed [(3
+
+
+
1] cycloaddition
of 1-yne/ene-vinylcyclopropanes and CO: homologous Pauson-Khand reaction and
the total synthesis of (
2)
-agarofuran.
Org. Lett.
,
12
, 2528-2531.
[61] (a) Jiao, L., Ye, S. and Yu, Z.-X. (2008) Rh(I)-catalyzed intramolecular [3
±
)-
α
2]
cycloaddition of
trans
-vinylcyclopropane-enes.
J. Am. Chem. Soc.
,
130
, 7178-7179;
(b) Jiao, L., Lin, M. and Yu, Z.-X. (2010) Rh(I)-catalyzed intramolecular [3
+
2]
cycloaddition reactions of 1-ene-, 1-yne- and 1-allene-vinylcyclopropanes.
Chem.
Commun.
, 46, 1059-1061; (c) Li, Q., Jiang, G.-J., Jiao, L., and Yu, Z.-X. (2010)
Reaction of
+
α
-ene-vinylcyclopropanes: type II intramolecular [5
+
2] cycloaddition or
2] cycloaddition?
Org. Lett.
,
12
, 1332-1335.
[62] Hayashi, Y., Miyakoshi, N., Kitagaki, S. and Mukai, C. (2008) Stereoselective total
syntheses of uncommon sesquiterpenoids isolated from
Jatropha neopauciflora
.
Org.
Lett.
,
10
, 2385-2388.
[63] Ishikawa, T., Ishii, H., Shimizu, K., Nakao, H., Urano, J., Kudo, T. and Saito, S.
(2004) Diastereoselective total synthesis of isocarbacyclin from L-ascorbid acid.
J. Org. Chem.
,
69
, 8133-8135.
[64] Belanger, D. B. and Livinghouse, T. (1998) Hexacarbonyldicobalt-alkyne complexes
as convenient Co
2
(CO)
8
surrogates in the catalytic Pauson-Khand reaction.
Tetrahe-
dron Lett.
,
39
, 7641-7644.
[65] Hasimoto, T., Tori, M., Taira, Z. and Asakawa, Y. (1985) New highly oxidized fusicoc-
cane diterpenoids from the liverwort
plagiochila acanthophylla japonica
.
Tetrahedron
Lett.
,
26
, 6473-6476.
[66] Nozoe, S., Morisaki, Tsuda, K., Iitaki, Y., Takahashi, T., Tamura, S., Ishibashi, K.
and Shirasaka. M. (1968) The structure of ophiobolin, a C
25
terpenoid having a novel
skeleton.
J. Am. Chem. Soc.
,
87
, 4968-4970.
[67] Sassa, T., Takahama, A. and Shindo, T. (1975) The stereostructure of cotylenol, the
aglycone of cotylenins leaf growth substances.
Agr. Biol. Chem.
,
39
, 1729-1734.
[68] Cao, H., Munda, S. R. and Cook, J. M. (2003) Studies on the Rh and Ir mediated
tandem Pauson-Khand reaction. A new entry into the dicyclopenta[a,d]cyclooctene
ring system.
Tetrahedron Lett.
,
44
, 6165-6168.
[69] Additional examples of the Pauson-Khand reaction in total synthesis: (a) Krafft, M.E.,
Cheung, Y.Y. and Abboud, K. A. (2001) Total synthesis of (
[3
+
)-asteriscanolide.
J. Org.
Chem.
,
66
, 7443-7448; (b) Ishizaki, M., Niimi, Y., Hoshino, O., Hara, H. and Taka-
hashi, T. (2005) A formal total synthesis of Lycopodium alkaloid, (
±
)-magellanine,
by using the intramolecular Pauson-Khand reaction.
Tetrahedron
,
61
, 4053-4065; (c)
Nakayama, A., Kogure, N., Kitajima, Lycopodium Alkaloids, Lycoposerramine-C and
±
