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Synthesis of Bisindole Alkaloids from the Apocynaceae Which Contain a Macroline or Sarpagine Unit: A Review

Bisindole natural products consist of two monomeric indole alkaloid units as their obligate constituents. Bisindoles are more potent with respect to their biological activity than their corresponding monomeric units. In addition, the synthesis of bisindoles are far more challenging than the synthesi...

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Autores principales: Rahman, Md Toufiqur, Tiruveedhula, Veera V. N. Phani Babu, Cook, James M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214337/
https://www.ncbi.nlm.nih.gov/pubmed/27854259
http://dx.doi.org/10.3390/molecules21111525
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author Rahman, Md Toufiqur
Tiruveedhula, Veera V. N. Phani Babu
Cook, James M.
author_facet Rahman, Md Toufiqur
Tiruveedhula, Veera V. N. Phani Babu
Cook, James M.
author_sort Rahman, Md Toufiqur
collection PubMed
description Bisindole natural products consist of two monomeric indole alkaloid units as their obligate constituents. Bisindoles are more potent with respect to their biological activity than their corresponding monomeric units. In addition, the synthesis of bisindoles are far more challenging than the synthesis of monomeric indole alkaloids. Herein is reviewed the enantiospecific total and partial synthesis of bisindole alkaloids isolated primarily from the Alstonia genus of the Apocynaceae family. The monomeric units belong to the sarpagine, ajmaline, macroline, vobasine, and pleiocarpamine series. An up-to-date discussion of their isolation, characterization, biological activity as well as approaches to their partial and total synthesis by means of both synthetic and biosynthetic strategies are presented.
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spelling pubmed-52143372017-01-05 Synthesis of Bisindole Alkaloids from the Apocynaceae Which Contain a Macroline or Sarpagine Unit: A Review Rahman, Md Toufiqur Tiruveedhula, Veera V. N. Phani Babu Cook, James M. Molecules Review Bisindole natural products consist of two monomeric indole alkaloid units as their obligate constituents. Bisindoles are more potent with respect to their biological activity than their corresponding monomeric units. In addition, the synthesis of bisindoles are far more challenging than the synthesis of monomeric indole alkaloids. Herein is reviewed the enantiospecific total and partial synthesis of bisindole alkaloids isolated primarily from the Alstonia genus of the Apocynaceae family. The monomeric units belong to the sarpagine, ajmaline, macroline, vobasine, and pleiocarpamine series. An up-to-date discussion of their isolation, characterization, biological activity as well as approaches to their partial and total synthesis by means of both synthetic and biosynthetic strategies are presented. MDPI 2016-11-14 /pmc/articles/PMC5214337/ /pubmed/27854259 http://dx.doi.org/10.3390/molecules21111525 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Rahman, Md Toufiqur
Tiruveedhula, Veera V. N. Phani Babu
Cook, James M.
Synthesis of Bisindole Alkaloids from the Apocynaceae Which Contain a Macroline or Sarpagine Unit: A Review
title Synthesis of Bisindole Alkaloids from the Apocynaceae Which Contain a Macroline or Sarpagine Unit: A Review
title_full Synthesis of Bisindole Alkaloids from the Apocynaceae Which Contain a Macroline or Sarpagine Unit: A Review
title_fullStr Synthesis of Bisindole Alkaloids from the Apocynaceae Which Contain a Macroline or Sarpagine Unit: A Review
title_full_unstemmed Synthesis of Bisindole Alkaloids from the Apocynaceae Which Contain a Macroline or Sarpagine Unit: A Review
title_short Synthesis of Bisindole Alkaloids from the Apocynaceae Which Contain a Macroline or Sarpagine Unit: A Review
title_sort synthesis of bisindole alkaloids from the apocynaceae which contain a macroline or sarpagine unit: a review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214337/
https://www.ncbi.nlm.nih.gov/pubmed/27854259
http://dx.doi.org/10.3390/molecules21111525
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