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Journal articles on the topic 'Tubifolidine'

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1

Shimizu, Satoshi, Ken Ohori, Takayoshi Arai, Hiroaki Sasai, and Masakatsu Shibasaki. "A Catalytic Asymmetric Synthesis of Tubifolidine." Journal of Organic Chemistry 63, no. 21 (October 1998): 7547–51. http://dx.doi.org/10.1021/jo981069g.

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2

Shimizu, Satoshi, Ken Ohori, Takayoshi Arai, Hiroaki Sasai, and Masakatsu Shibasaki. "ChemInform Abstract: A Catalytic Asymmetric Synthesis of Tubifolidine." ChemInform 30, no. 13 (June 17, 2010): no. http://dx.doi.org/10.1002/chin.199913255.

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3

Uludag, Nesimi. "An Effective Approach to the Strychnos Alkaloids: Total Synthesis of Tubifolidine." Chemistry of Natural Compounds 57, no. 3 (May 2021): 491–96. http://dx.doi.org/10.1007/s10600-021-03394-y.

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4

Amat, Mercedes, M. Dolors Coll, Joan Bosch, Enric Espinosa, and Elies Molins. "Total syntheses of the Strychnos indole alkaloids(−)-tubifoline, (−)-tubifolidine, and (−)-19,20-dihydroakuammicine." Tetrahedron: Asymmetry 8, no. 6 (March 1997): 935–48. http://dx.doi.org/10.1016/s0957-4166(97)00071-2.

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5

Amat, Mercedes, Ana Linares, M. Luisa Salas, Mercedes Alvarez, and Joan Bosch. "A new strategy for the synthesis of pentacyclic Strychnos alkaloids: synthesis of (±)-tubifolidine." J. Chem. Soc., Chem. Commun., no. 6 (1988): 420–21. http://dx.doi.org/10.1039/c39880000420.

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6

AMAT, M., M. D. COLL, J. BOSCH, E. ESPINOSA, and E. MOLINS. "ChemInform Abstract: Total Syntheses of the Strychnos Indole Alkaloids (-)-Tubifoline, (-)- Tubifolidine, and (-)-19,20-Dihydroakuammicine." ChemInform 28, no. 31 (August 3, 2010): no. http://dx.doi.org/10.1002/chin.199731194.

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7

Amat, Mercedes, Ana Linares, and Joan Bosch. "A new synthetic entry to pentacyclic Strychnos alkaloids. Total synthesis of (.+-.)-tubifolidine, (.+-.)-tubifoline, and (.+-.)-19,20-dihydroakuammicine." Journal of Organic Chemistry 55, no. 26 (December 1990): 6299–312. http://dx.doi.org/10.1021/jo00313a017.

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8

Kim, Dong-Hyun, Jeong-Hwa Kim, Tae-Hong Jeon, and Cheon-Gyu Cho. "New Synthetic Routes to (+)-Uleine and (−)-Tubifolidine: General Approach to 2-Azabicyclo[3.3.1]nonane Indole Alkaloids." Organic Letters 22, no. 9 (April 13, 2020): 3464–68. http://dx.doi.org/10.1021/acs.orglett.0c00912.

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9

AMAT, M., A. LINARES, and J. BOSCH. "ChemInform Abstract: A New Synthetic Entry to Pentacyclic Strychnos Alkaloids. Total Synthesis of (.+-.)-Tubifolidine, (.+-.)-Tubifoline, and (.+-.)-19,20- Dihydroakuammicine." ChemInform 22, no. 27 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199127262.

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10

Serdaroğlu, Goncagul, Nesimi Uludag, Paramasivam Sugumar, and Parthasarathi Rajkumar. "(-)-Tubifolidine as strychnos indole alkaloid: Spectroscopic charactarization (FT-IR, NMR, UV-Vis), antioxidant activity, molecular docking, and DFT studies." Journal of Molecular Structure 1244 (November 2021): 130978. http://dx.doi.org/10.1016/j.molstruc.2021.130978.

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11

Alvarez, Mercades, Marisa Salas, Anna de Veciana, Rodolfo Lavilla, and Joan Bosch. "Nucleophilic addition of indole-2-acetic ester enolates to N-alkylpyridinium salts. A formal synthesis of the strychnos alkaloids tubifolidine and tubifoline." Tetrahedron Letters 31, no. 35 (January 1990): 5089–92. http://dx.doi.org/10.1016/s0040-4039(00)97813-4.

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12

ALVAREZ, M., M. SALAS, A. DE VECIANA, R. LAVILLA, and J. BOSCH. "ChemInform Abstract: Nucleophilic Addition of Indole-2-acetic Ester Enolates to N- Alkylpyridinium Salts. A Formal Synthesis of the Strychnos Alkaloids Tubifolidine and Tubifoline." ChemInform 23, no. 19 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199219310.

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13

Solé, Daniel, Josep Bonjoch, Silvina García-Rubio, Ramon Suriol, and Joan Bosch. "A new solution for the construction of the piperidine ring of strychnos alkaloids from 3a-(o-nitrophenyl)hexahydroindol-4-ones. Total syntheses of (±)-tubifolidine, (±)-dihydroakuammicine, and (±)-akuammicine." Tetrahedron Letters 37, no. 29 (July 1996): 5213–16. http://dx.doi.org/10.1016/0040-4039(96)01054-4.

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14

SOLE, D., J. BONJOCH, S. GARCIA-RUBIO, R. SURIOL, and J. BOSCH. "ChemInform Abstract: A New Solution for the Construction of the Piperidine Ring of Strychnos Alkaloids from 3a-(o-Nitrophenyl)hexahydroindol-4-ones. Total Syntheses of (.+-.)-Tubifolidine, (.+-.)-Dihydroakuammicine, and (.+-.)-Akuammicine." ChemInform 27, no. 42 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199642232.

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15

BONJOCH, J., D. SOLE, S. GARCIA-RUBIO, and J. BOSCH. "ChemInform Abstract: A General Synthetic Entry to Strychnos Alkaloids of the Curan Type via a Common 3a-(2-Nitrophenyl)hexahydroindol-4-one Intermediate. Total Syntheses of (.+-.)- and (-)-Tubifolidine, (.+-.)-Akuammicine, (.+-.)- 19,20-Dihydroakuammicine." ChemInform 28, no. 48 (August 2, 2010): no. http://dx.doi.org/10.1002/chin.199748262.

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16

Bonjoch, Josep, Daniel Solé, Silvina García-Rubio, and Joan Bosch. "A General Synthetic Entry toStrychnosAlkaloids of the Curan Type via a Common 3a-(2-Nitrophenyl)hexahydroindol-4-one Intermediate. Total Syntheses of (±)- and (−)-Tubifolidine, (±)-Akuammicine, (±)-19,20-Dihydroakuammicine, (±)-Norfluorocurarine, (±)-Echitamidine, and (±)-20-Epilochneridine1." Journal of the American Chemical Society 119, no. 31 (August 1997): 7230–40. http://dx.doi.org/10.1021/ja970347a.

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