Relevant bibliographies by topics / Tubifolidine

Academic literature on the topic 'Tubifolidine'

Author: Grafiati
Published: 6 September 2023
Last updated: 7 September 2023

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Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Tubifolidine.'

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Journal articles on the topic "Tubifolidine"

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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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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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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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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Dissertations / Theses on the topic "Tubifolidine"

1

Khandare, Sopan Pralhad. "Total Synthesis of Piperidine and Pyrrolidine Alkaloids and Towards the Total Synthesis of Strychnine." Thesis, 2022. https://etd.iisc.ac.in/handle/2005/5817.

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Abstract:
Total synthesis of natural products is an important area of contemporary interest in synthetic organic chemistry. Total synthesis of natural products serves as a platform for the development of new synthetic strategies and for improving the existing synthetic methods. Chiral sulfinimines are excellent substrates for the synthesis of amine-containing compounds. The ability of sulfinimines in rendering the product amines with consistent high selectivity has made these reagents one of the most used reagents in organic synthesis. The thesis describes the investigations concerning the addition of nucleophiles such as the Wittig Ylides, and benzyloxy ketones to sulfinimines. Application of the formed products in the synthesis of piperidine, pyrrolidine alkaloids, and in the total synthesis of strychnine is described.
SERB, Grant No. CRG/2018/001332
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