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Results: 1-7 |
Results: 7
A new method for the demetallation of tricarbonyliron diene complexes by total hydrogenation with Raney nickel. Application to a very short synthesisof (+)-[6]-gingerdiol
Authors: Franck-Neumann, M Geoffroy, P Bissinger, P Adelaide, S
Citation: M. Franck-neumann et al., A new method for the demetallation of tricarbonyliron diene complexes by total hydrogenation with Raney nickel. Application to a very short synthesisof (+)-[6]-gingerdiol, TETRAHEDR L, 42(36), 2001, pp. 6401-6404
Highly stereoselective total synthesis of multiply protected 3-amino-3,6-dideoxyaldohexoses (mycosamine/mycaminose) by aldol condensation reaction, mediated by tin triflate, of tricarbonyliron/alpha-amimodienone complexes
Authors: Franck-Neumann, M Miesch-Gross, L Gateau, C
Citation: M. Franck-neumann et al., Highly stereoselective total synthesis of multiply protected 3-amino-3,6-dideoxyaldohexoses (mycosamine/mycaminose) by aldol condensation reaction, mediated by tin triflate, of tricarbonyliron/alpha-amimodienone complexes, EUR J ORG C, (22), 2000, pp. 3693-3702
Aldol condensation reactions of tricarbonyliron complexes. Easy access to diastereomerically pure 1,2,3-trisubstituted 1,3-diols from alpha-substituted dienone complexes
Authors: Franck-Neumann, M Geoffroy, P Gumery, F Bissinger, P
Citation: M. Franck-neumann et al., Aldol condensation reactions of tricarbonyliron complexes. Easy access to diastereomerically pure 1,2,3-trisubstituted 1,3-diols from alpha-substituted dienone complexes, TETRAHEDR L, 41(21), 2000, pp. 4213-4217
Aldol condensation reactions of tricarbonyliron complexes. Towards building blocks for the synthesis of carbomycin B/tylosin macrolide antibiotics and fluorinated analogs
Authors: Franck-Neumann, M Geoffroy, P Gumery, F
Citation: M. Franck-neumann et al., Aldol condensation reactions of tricarbonyliron complexes. Towards building blocks for the synthesis of carbomycin B/tylosin macrolide antibiotics and fluorinated analogs, TETRAHEDR L, 41(21), 2000, pp. 4219-4222
Uncatalyzed [2+2] cycloaddition of cyclic ketenetrimethylsilylacetals withelectrophilic acetylenes.
Authors: Miesch, M Wendling, F Franck-Neumann, M
Citation: M. Miesch et al., Uncatalyzed [2+2] cycloaddition of cyclic ketenetrimethylsilylacetals withelectrophilic acetylenes., TETRAHEDR L, 40(5), 1999, pp. 839-842
Cyclization and fluorination of 5-hexenols with boron trifluoride etherate. Stereoselective synthesis of (optically active) fluorinated cyclohexane derivatives by cyclization of omega-pentenyl pentadienol tricarbonyl iron complexes.
Authors: Franck-Neumann, M Geoffroy, P Hanss, D
Citation: M. Franck-neumann et al., Cyclization and fluorination of 5-hexenols with boron trifluoride etherate. Stereoselective synthesis of (optically active) fluorinated cyclohexane derivatives by cyclization of omega-pentenyl pentadienol tricarbonyl iron complexes., TETRAHEDR L, 40(48), 1999, pp. 8487-8490
Highly stereoselective synthesis of 3-amino-3,6-dideoxy-aldohexoses by tintriflate mediated aldol condensation reaction of tricarbonyl iron alpha-aminodienone complexes. Total synthesis of multiprotected mycosamine.
Authors: Franck-Neumann, M Miesch-Gross, L Gateau, C
Citation: M. Franck-neumann et al., Highly stereoselective synthesis of 3-amino-3,6-dideoxy-aldohexoses by tintriflate mediated aldol condensation reaction of tricarbonyl iron alpha-aminodienone complexes. Total synthesis of multiprotected mycosamine., TETRAHEDR L, 40(14), 1999, pp. 2829-2832
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