-
1
-
-
0042462010
-
-
Picralima nitida Th. and H. Durand, syn P. klaineana Pierre
-
Picralima nitida Th. and H. Durand, syn P. klaineana Pierre.
-
-
-
-
4
-
-
37049046031
-
-
At the same time, Joule and Smith converted akuammine into pseudoakuammigine, and reported partial structures for both bases
-
At the same time, Joule and Smith converted akuammine into pseudoakuammigine, and reported partial structures for both bases: Joule, J. A.; Smith, G. F. J. Chem. Soc. 1962, 312.
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J. Chem. Soc.
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Joule, J.A.1
Smith, G.F.2
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5
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37049041777
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Hamilton, J. A.; Hamor, T. A.; Robertson, J. M.; Sim, G. A. Proc. Chem. Soc., 1961, 63.
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Proc. Chem. Soc.
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Hamilton, J.A.1
Hamor, T.A.2
Robertson, J.M.3
Sim, G.A.4
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7
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0003567908
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Olivier, L.; Lévy, J.; Le Men, J.; Janot, M.-M.; Budzikiewicz, H.; Djerassi, C. Bull. Soc. Chim. France 1965, 868.
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Olivier, L.1
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8
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Southon, J.W.1
Buckingham, J.2
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0001002028
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Indoles, The Monoterpenoid Indole Alkaloids Saxton, J. E., Ed. Weissberger, A., Taylor, E. C., Eds.; Wiley: New York
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Joule, J. A. In Indoles, The Monoterpenoid Indole Alkaloids; Saxton, J. E., Ed. In The Chemistry of Heterocyclic Compounds; Weissberger, A., Taylor, E. C., Eds.; Wiley: New York, 1983; Vol. 25, Part 4, pp 244-264.
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Joule, J.A.1
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0000404240
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The Monoterpenoid Indole Alkaloids Saxton, J. E., Ed. Taylor, E. C., Ed.; Wiley: Chichester
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Alvarez, M.; Joule, J. In The Monoterpenoid Indole Alkaloids; Saxton, J. E., Ed. In The Chemistry of Heterocyclic Compounds; Taylor, E. C., Ed.; Wiley: Chichester, 1994; Vol. 25, Supplement to Part 4, pp 248-259.
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Alvarez, M.1
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0003870273
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Pelletier, S. W., Ed.; Wiley: New York Chapter 5
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Kisakürek, M. V.; Leeuwenberg, A. J. M.; Hesse, M. In Alkaloids: Chemical and Biological Perspectives; Pelletier, S. W., Ed.; Wiley: New York, 1983; Chapter 5.
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Kisakürek, M.V.1
Leeuwenberg, A.J.M.2
Hesse, M.3
-
14
-
-
0013848559
-
-
The biogenetic numbering used to label the parent geissoschizine (5) is utilized throughout the review for all monoterpenoid alkaloids and related structures
-
The biogenetic numbering used to label the parent geissoschizine (5) is utilized throughout the review for all monoterpenoid alkaloids and related structures. Le Men, J.; Taylor, W. I. Experientia 1965, 21, 508.
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Experientia
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Le Men, J.1
Taylor, I.2
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15
-
-
0042963150
-
-
Semiempirical MO calculations (PM3 and AM1 methods) were performed using the MOPAC package of programs. MOPAC 97, Fujitsu Limited, Tokyo, Japan
-
Semiempirical MO calculations (PM3 and AM1 methods) were performed using the MOPAC package of programs: Stewart, J. J. P. MOPAC 97, Fujitsu Limited, Tokyo, Japan, 1997.
-
(1997)
-
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Stewart, J.J.P.1
-
16
-
-
0017398772
-
-
Strictamine yields akuammicine in poor yields upon basic treatment throughout a sequence of anionic rearrangements that is proposed to involve the following intermediates
-
Ahmad, Y.; Fatima, K.; Rahman, A.; Occolowitz, J. L.; Solheim, B. A.; Clardy, J.; Garnick, R. L.; Le Quesne, P. W. J. Am. Chem. Soc. 1977, 99, 1943. Strictamine yields akuammicine in poor yields upon basic treatment throughout a sequence of anionic rearrangements that is proposed to involve the following intermediates:
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Ahmad, Y.1
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Hugel, G.; Royer, D.; Le Men-Olivier, L.; Richard, B.; Jacquier, M.-J.; Lévy, J. J. Org. Chem. 1997, 62, 578.
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Ito, M.; Clark, C. W.; Mortimore, M.; Goh, J. B.; Martin, S. F. J. Am. Chem. Soc. 2001, 118, 9804.
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0000963033
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For representative chemical correlations, see
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For representative chemical correlations, see: Massiot, G.; Lavaud, C.; Vercauteren, J.; Le Men-Olivier, L.; Lévy, J. Helv. Chim. Acta 1983, 66, 2414.
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Massiot, G.1
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Banerji, J.; Chakrabarti, R. Indian J. Chem., Sect. B, 1984, 23, 453.
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0041961386
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See also references [9], [10], and [14]
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26
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0030840651
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Syntheses of akuammicine
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Syntheses of akuammicine: Bonjoch, J.; Solé, D.; García-Rubio, S.; Bosch, J. J. Am. Chem. Soc. 1997; 119, 7230.
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For Martin's approach, see references [17] and [18]. With the exception of the Wieland-Gumlich aldehyde and strychnine, over 40 total syntheses of pentacyclic Strychnos alkaloids have been accomplished, for a premium review, see
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For Martin's approach, see references [17] and [18]. With the exception of the Wieland-Gumlich aldehyde and strychnine, over 40 total syntheses of pentacyclic Strychnos alkaloids have been accomplished, for a premium review, see: Bonjoch, J.; Solé, D. Chem. Rev. 2000, 100, 3455.
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0027716570
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Alkaloids with the pleiocarpamine skeleton compose a related family of bases that differ from akuammiline alkaloids in the regioselective closure of ring E between N-1 and C-16. The total syntheses of (±)-2,7-dihydropleiocarpamine, (± -16-epi-pleiocarpamine, and (±)-nor-mavacurine have been reported in addition to the partial synthesis of (+)-16-epi-pleiocarpamine, and the elaboration of pattern structures
-
Alkaloids with the pleiocarpamine skeleton compose a related family of bases that differ from akuammiline alkaloids in the regioselective closure of ring E between N-1 and C-16. The total syntheses of (±)-2,7-dihydropleiocarpamine, (± -16-epi-pleiocarpamine, and (±)-nor-mavacurine have been reported in addition to the partial synthesis of (+)-16-epi-pleiocarpamine, and the elaboration of pattern structures: Bennasar, M.-L.; Zulaica, E.; Jiménez, J.-M.; Bosch, J. J. Org. Chem. 1993, 58, 7756.
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0041961381
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Pentacycle 56a contains the reverse pleiocarpamine skeleton defined by see reference [15]
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Pentacycle 56a contains the reverse pleiocarpamine skeleton defined by Hugel et al.; see reference [15].
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Hugel, A.1
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The search of chemical abstracts was executed on SciFinder. The authors of this Review ask to be excused for the involuntary absence of any references regarding the isolation of akuammiline alkaloids within the period covered
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The search of chemical abstracts was executed on SciFinder. The authors of this Review ask to be excused for the involuntary absence of any references regarding the isolation of akuammiline alkaloids within the period covered.
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