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Journal articles on the topic 'Aspidospermatane'

Author: Grafiati
Published: 4 June 2021
Last updated: 5 February 2022

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1

Reina, Matías, Wilfredo Ruiz-Mesia, Lastenia Ruiz-Mesia, Rafael Martínez-Díaz, and Azucena González-Coloma. "Indole Alkaloids from Aspidosperma rigidum and A. schultesii and their Antiparasitic Effects." Zeitschrift für Naturforschung C 66, no. 5-6 (June 1, 2011): 225–34. http://dx.doi.org/10.1515/znc-2011-5-605.

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Five oxindole alkaloids, three plumerane-type alkaloids, subtype haplophitine, and one aspidospermatane-type alkaloid, subtype tubotaiwine, were isolated from the medicinal plants Aspidosperma rigidum and A. schultesii. One compound was identified as the transoid conformer of 18-oxo-O-methylaspidoalbine which was not previously described. The antiparasitic activity of all compounds against Trypanosoma cruzi and Leishmania infantum and their non-specific cytotoxicity against mammalian cells were also determined.
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2

Gan, Chew-Yan, Yun-Yee Low, Ward T. Robinson, Kanki Komiyama, and Toh-Seok Kam. "Aspidospermatan–aspidospermatan and eburnane-sarpagine bisindole alkaloids from Leuconotis." Phytochemistry 71, no. 11-12 (August 2010): 1365–70. http://dx.doi.org/10.1016/j.phytochem.2010.05.015.

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3

Kuehne, Martin E., and Feng Xu. "Total synthesis of strychnan and aspidospermatan alkaloids. 3. The total synthesis of (.+-.)-strychnine." Journal of Organic Chemistry 58, no. 26 (December 1993): 7490–97. http://dx.doi.org/10.1021/jo00078a030.

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4

Morita, Hiroshi, Kartini Ahmad, Yusuke Hirasawa, Alfarius Eko Nugroho, and A. Hamid A. Hadi. "NEW ASPIDOFRACTININE, ASPIDOSPERMATAN AND AKUAMILINE INDOLE ALKALOIDS FROM THE ROOTS OF KOPSIA SINGAPURENSIS RIDL." HETEROCYCLES 86, no. 2 (2012): 1611. http://dx.doi.org/10.3987/com-12-s(n)113.

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5

Kuehne, Martin E., Christopher S. Brook, Deborah A. Frasier, and Feng Xu. "Syntheses of Strychnos- and Aspidospermatan-Type Alkaloids. 7. Total Syntheses of Lagunamine, Isolagunamine, Condylocarpine, and Isocondylocarpine." Journal of Organic Chemistry 60, no. 6 (March 1995): 1864–67. http://dx.doi.org/10.1021/jo00111a053.

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6

Hauduc, Clémence, and Guillaume Bélanger. "General Approach toward Aspidospermatan-Type Alkaloids Using One-Pot Vilsmeier–Haack Cyclization and Azomethine Ylide Cycloaddition." Journal of Organic Chemistry 82, no. 9 (April 18, 2017): 4703–12. http://dx.doi.org/10.1021/acs.joc.7b00345.

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7

Ahmad, Kartini, Yusuke Hirasawa, Alfarius Eko Nugroho, A. Hamid A. Hadi, and Hiroshi Morita. "ChemInform Abstract: New Aspidofractinine, Aspidospermatan and Akuamiline Indole Alkaloids from the Roots of Kopsia singapurensis Ridl." ChemInform 44, no. 17 (April 4, 2013): no. http://dx.doi.org/10.1002/chin.201317205.

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8

Parsons, Rodney L., Jeffrey D. Berk, and Martin E. Kuehne. "Total synthesis of strychnan- and aspidospermatan-type alkaloids. 2. Generation of 15-(3-furanyl) ABCE tetracyclic intermediates." Journal of Organic Chemistry 58, no. 26 (December 1993): 7482–89. http://dx.doi.org/10.1021/jo00078a029.

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9

KUEHNE, M. E., and F. XU. "ChemInform Abstract: Total Synthesis of Strychnan and Aspidospermatan Alkaloids. Part 3. The Total Synthesis of (.+-.)-Strychnine (V)." ChemInform 25, no. 17 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199417241.

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10

Kuehne, Martin E., and Feng Xu. "Syntheses of Strychnan- and Aspidospermatan-Type Alkaloids. 10. An Enantioselective Synthesis of (−)-Strychnine through the Wieland−Gumlich Aldehyde." Journal of Organic Chemistry 63, no. 25 (December 1998): 9427–33. http://dx.doi.org/10.1021/jo9813989.

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11

Kuehne, Martin E., and Feng Xu. "Syntheses of Strychnan- and Aspidospermatan-Type Alkaloids. 11. Total Syntheses of (−)-Lochneridine and (−)- and Racemic 20-epi-Lochneridine." Journal of Organic Chemistry 63, no. 25 (December 1998): 9434–39. http://dx.doi.org/10.1021/jo981401o.

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12

Kuehne, Martin E., Feng Xu, and Christopher S. Brook. "Syntheses of Strychnos- and Aspidospermatan-Type Alkaloids. 6. Total Syntheses of (.+-.)-Echitamidine, (.+-.)-Alstogustine, (.+-.)-19-epi-Alstogustine, and (.+-.)-Akuammicine." Journal of Organic Chemistry 59, no. 25 (December 1994): 7803–6. http://dx.doi.org/10.1021/jo00104a042.

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13

Kuehne, M. E., C. S. Brook, and D. A. Frasier. "Syntheses of Strychnos and Aspidospermatan Type Alkaloids. 4. Formation of the Pentacyclic Core by an Intramolecular Diels Alder Reaction." Natural Product Letters 4, no. 1 (February 1994): 65–72. http://dx.doi.org/10.1080/10575639408043894.

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14

PARSONS, R. L., J. D. BERK, and M. E. KUEHNE. "ChemInform Abstract: Total Syntheses of Strychnan- and Aspidospermatan-Type Alkaloids. Part 2. Generation of 15-(3-Furanyl) ABCE Tetracyclic Intermediates." ChemInform 25, no. 17 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199417240.

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15

Kuehne, Martin E., Christopher S. Brook, Deborah A. Frasier, and Feng Xu. "Syntheses of Strychnos- and Aspidospermatan-Type Alkaloids. 5. Total Syntheses of (.+-.)-Echitamidine and 20-epi- and 19-epi-20-epi-Echitamidine." Journal of Organic Chemistry 59, no. 20 (October 1994): 5977–82. http://dx.doi.org/10.1021/jo00099a029.

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16

Kuehne, Martin E., and Feng Xu. "ChemInform Abstract: Syntheses of Strychnan- and Aspidospermatan-Type Alkaloids. Part 10. An Enantioselective Synthesis of (-)-Strychnine Through the Wieland-Gumlich Aldehyde." ChemInform 30, no. 23 (June 15, 2010): no. http://dx.doi.org/10.1002/chin.199923243.

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17

Kuehne, Martin E., and Feng Xu. "ChemInform Abstract: Syntheses of Strychnan- and Aspidospermatan-Type Alkaloids. Part 11. Total Syntheses of (-)-Lochneridine and (-)- and Racemic 20-epi-Lochneridine." ChemInform 30, no. 23 (June 15, 2010): no. http://dx.doi.org/10.1002/chin.199923244.

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18

KUEHNE, M. E., F. XU, and C. S. BROOK. "ChemInform Abstract: Syntheses of Strychnos- and Aspidospermatan-Type Alkaloids. Part 6. Total Syntheses of (.+-.)-Echitamidine, (.+-.)-Alstogustine, (.+-.)-19- epi-Alstogustine, and (.+-.)-Akuammicine." ChemInform 26, no. 26 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199526229.

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19

Kuehne, Martin E., Tiansheng Wang, and Denis Seraphin. "Syntheses of Strychnos and Aspidospermatan-Type Alkaloids. 8. Selective Total Syntheses of Mossambine and 14-epi-Mossambine by a Radical Cyclization Reaction1." Journal of Organic Chemistry 61, no. 22 (January 1996): 7873–81. http://dx.doi.org/10.1021/jo961023s.

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20

Kuehne, Martin E., and Feng Xu. "Syntheses of Strychnan- and Aspidospermatan-Type Alkaloids. 9.1The Enantioselective Generation of Tetracyclic ABCE Intermediates by a Tandem Condensation, [3,3]-Sigmatropic Rearrangement, and Cyclization Sequence." Journal of Organic Chemistry 62, no. 23 (November 1997): 7950–60. http://dx.doi.org/10.1021/jo970207j.

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21

KUEHNE, M. E., C. S. BROOK, D. A. FRASIER, and F. XU. "ChemInform Abstract: Syntheses of Strychnos- and Aspidospermatan-Type Alkaloids. Part 5. Total Syntheses of (.+-.)-Echitamidine and 20-epi- and 19-epi-20-epi- Echitamidine." ChemInform 26, no. 18 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199518259.

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22

KUEHNE, M. E., T. WANG, and D. SERAPHIN. "ChemInform Abstract: Syntheses of Strychnos and Aspidospermatan-Type Alkaloids. Part 8. Selective Total Syntheses of Mossambine and 14-epi-Mossambine by a Radical Cyclization Reaction." ChemInform 28, no. 11 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199711211.

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23

KUEHNE, M. E., and F. XU. "ChemInform Abstract: Syntheses of Strychnan- and Aspidospermatan-Type Alkaloids. Part 9. The Enantioselective Generation of Tetracyclic ABCE Intermediates by a Tandem Condensation, [3,3]-Sigmatropic Rearrangement, and Cyclization Sequence." ChemInform 29, no. 15 (June 23, 2010): no. http://dx.doi.org/10.1002/chin.199815232.

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