Literature DB >> 26827883

Sarpagine and Related Alkaloids.

Ojas A Namjoshi1, James M Cook2.   

Abstract

The sarpagine-related macroline and ajmaline alkaloids share a common biosynthetic origin, and bear important structural similarities, as expected. These indole alkaloids are widely dispersed in 25 plant genera, principally in the family Apocynaceae. Very diverse and interesting biological properties have been reported for this group of natural products. Isolation of new sarpagine-related alkaloids and the asymmetric synthesis of these structurally complex molecules are of paramount importance to the synthetic and medicinal chemists. A total of 115 newly isolated sarpagine-related macroline and ajmaline alkaloids, along with their physicochemical properties have been included in this chapter. A general and efficient strategy for the synthesis of these monomeric alkaloids, as well as bisindoles, has been presented, which involves application of the asymmetric Pictet-Spengler reaction (>98% ee) as a key step because of the ease of scale up of the tetracyclic template. Also included in this chapter are the syntheses of the sarpagine-related alkaloids, published since 2000.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Ajmaline; Biosynthesis; Enantioselective; Macroline; Nature-inspired; Pictet–Spengler reaction; Sarpagine

Mesh:

Substances:

Year:  2015        PMID: 26827883      PMCID: PMC4864735          DOI: 10.1016/bs.alkal.2015.08.002

Source DB:  PubMed          Journal:  Alkaloids Chem Biol        ISSN: 1099-4831


  85 in total

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Authors:  Jianming Yu; Xiangyu Z Wearing; James M Cook
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Authors:  G Pasquali; O J Goddijn; A de Waal; R Verpoorte; R A Schilperoort; J H Hoge; J Memelink
Journal:  Plant Mol Biol       Date:  1992-04       Impact factor: 4.076

7.  Synthesis of bridged azabicyclic structures via ring-closing olefin metathesis.

Authors:  Christopher E Neipp; Stephen F Martin
Journal:  J Org Chem       Date:  2003-11-14       Impact factor: 4.354

8.  Stereospecific approach to the synthesis of ring-A oxygenated sarpagine indole alkaloids. Total synthesis of the dimeric indole alkaloid P-(+)-dispegatrine and six other monomeric indole alkaloids.

Authors:  Chitra R Edwankar; Rahul V Edwankar; Ojas A Namjoshi; Xuebin Liao; James M Cook
Journal:  J Org Chem       Date:  2013-06-18       Impact factor: 4.354

9.  Alstiphyllanines I-O, ajmaline type alkaloids from Alstonia macrophylla showing vasorelaxant activity.

Authors:  Hiroko Arai; Kazumasa Zaima; Erika Mitsuta; Haruka Tamamoto; Aiko Saito; Yusuke Hirasawa; Abdul Rahman; Idha Kusumawati; Noor Cholies Zaini; Hiroshi Morita
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Authors:  Rahul V Edwankar; Chitra R Edwankar; Jeffrey R Deschamps; James M Cook
Journal:  J Org Chem       Date:  2014-10-15       Impact factor: 4.354

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Review 3.  Synthesis of Bisindole Alkaloids from the Apocynaceae Which Contain a Macroline or Sarpagine Unit: A Review.

Authors:  Md Toufiqur Rahman; Veera V N Phani Babu Tiruveedhula; James M Cook
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Review 4.  Chemical Diversity and Bioactivities of Monoterpene Indole Alkaloids (MIAs) from Six Apocynaceae Genera.

Authors:  Afrah E Mohammed; Zainab H Abdul-Hameed; Modhi O Alotaibi; Nahed O Bawakid; Tariq R Sobahi; Ahmed Abdel-Lateff; Walied M Alarif
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5.  Completion of the Total Synthesis of Several Bioactive Sarpagine/Macroline Alkaloids including the Important NF-κB Inhibitor N4-Methyltalpinine.

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Review 6.  Bisindole Alkaloids from the Alstonia Species: Recent Isolation, Bioactivity, Biosynthesis, and Synthesis.

Authors:  Kamal P Pandey; Md Toufiqur Rahman; James M Cook
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