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Results: 1-11 |
Results: 11
New palladium-catalysed access to 3-(1 '-indanylidene) phthalide, precursor of the core of fredericamycin A
Authors: Bouyssi, D Balme, G
Citation: D. Bouyssi et G. Balme, New palladium-catalysed access to 3-(1 '-indanylidene) phthalide, precursor of the core of fredericamycin A, SYNLETT, (7), 2001, pp. 1191-1193
Synthesis of heterocycles via sequential Pd/Ru-catalysed allene insertion-nucleophile incorporation-olefin metathesis
Authors: Dondas, HA Balme, G Blandine, C Grigg, R Hodgeson, A Morris, J Sridharan, V
Citation: Ha. Dondas et al., Synthesis of heterocycles via sequential Pd/Ru-catalysed allene insertion-nucleophile incorporation-olefin metathesis, TETRAHEDR L, 42(49), 2001, pp. 8673-8675
An effective one-pot synthesis of 3-benzylfurans and their potential utility as versatile precursors of 3,4-dibenzyltetrahydrofuran lignans. Formal synthesis of (+/-)-burseran
Authors: Garcon, S Vassiliou, S Cavicchioli, M Hartmann, B Monteiro, N Balme, G
Citation: S. Garcon et al., An effective one-pot synthesis of 3-benzylfurans and their potential utility as versatile precursors of 3,4-dibenzyltetrahydrofuran lignans. Formal synthesis of (+/-)-burseran, J ORG CHEM, 66(11), 2001, pp. 4069-4073
A versatile palladium-mediated three-component reaction for the one-pot synthesis of stereodefined 3-arylidene-(or 3-alkenylidene-)tetrahydrofurans
Authors: Bottex, M Cavicchioli, M Hartmann, B Monteiro, N Balme, G
Citation: M. Bottex et al., A versatile palladium-mediated three-component reaction for the one-pot synthesis of stereodefined 3-arylidene-(or 3-alkenylidene-)tetrahydrofurans, J ORG CHEM, 66(1), 2001, pp. 175-179
The effect of the carbon ligand on the reaction of organozinc reagents in the synthesis of substituted 2,5-dihydrofurans: A rare example of an uncatalysed allylic-substitution reaction involving alkyl zinc halides
Authors: Woods, M Monteiro, N Balme, G
Citation: M. Woods et al., The effect of the carbon ligand on the reaction of organozinc reagents in the synthesis of substituted 2,5-dihydrofurans: A rare example of an uncatalysed allylic-substitution reaction involving alkyl zinc halides, EUR J ORG C, (9), 2000, pp. 1711-1718
Rearrangement of oxaspiroheptanes to cyclohexanones mediated by lithium iodide
Authors: Bouyssi, D Cavicchioli, M Large, S Monteiro, N Balme, G
Citation: D. Bouyssi et al., Rearrangement of oxaspiroheptanes to cyclohexanones mediated by lithium iodide, SYNLETT, (5), 2000, pp. 749-751
2-aza [2,2,1] bicyclo heptane derivatives: ring expansion, fragmentation and synthesis of a potential TxA(2) antagonist
Authors: Perrin, V Riveron, V Balme, G Gore, J
Citation: V. Perrin et al., 2-aza [2,2,1] bicyclo heptane derivatives: ring expansion, fragmentation and synthesis of a potential TxA(2) antagonist, J CHEM R-S, (2), 2000, pp. 60-61
Palladium-catalyzed reaction of propargyl nucleophiles with alpha-sulfonylalpha,beta-unsaturated ketones: A single-step synthesis of furo[3,4-c] heterocyclic derivatives
Authors: Monteiro, N Balme, G
Citation: N. Monteiro et G. Balme, Palladium-catalyzed reaction of propargyl nucleophiles with alpha-sulfonylalpha,beta-unsaturated ketones: A single-step synthesis of furo[3,4-c] heterocyclic derivatives, J ORG CHEM, 65(10), 2000, pp. 3223-3226
Intramolecular carbocupration reaction of unactivated alkynes bearing a stabilized nucleophile: Application to the synthesis of iridoid monoterpenes.
Authors: Bouyssi, D Monteiro, N Balme, G
Citation: D. Bouyssi et al., Intramolecular carbocupration reaction of unactivated alkynes bearing a stabilized nucleophile: Application to the synthesis of iridoid monoterpenes., TETRAHEDR L, 40(7), 1999, pp. 1297-1300
A one pot synthesis of various Pyrrolidines via a tandem Michael addition-transition metal-catalysed cyclisation reaction.
Authors: Clique, B Monteiro, N Balme, G
Citation: B. Clique et al., A one pot synthesis of various Pyrrolidines via a tandem Michael addition-transition metal-catalysed cyclisation reaction., TETRAHEDR L, 40(7), 1999, pp. 1301-1304
Synthesis of potential thromboxane A(2) antagonists based on the azabicyclo[2.2.1]heptane skeleton
Authors: Perrin, V Riveron, V Traversa, C Balme, G Gore, J
Citation: V. Perrin et al., Synthesis of potential thromboxane A(2) antagonists based on the azabicyclo[2.2.1]heptane skeleton, J CHEM R-S, (12), 1998, pp. 736-737A
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