Literature DB >> 22308756

The pyrrolo[2,1-a]isoquinoline alkaloids.

Ulrike Pässler1, Hans-Joachim Knölker.   

Abstract

The present chapter describes isolation, biogenetic proposals, and syntheses of the natural products 1-4 and 10-11 with a pyrrolo[2,1-a]-isoquinoline framework. Moreover, the syntheses of some structural analogs are discussed. The pyrrolo[2,1-a]isoquinolines are of interest due to their promising biological activities. For crispine A (1), many total syntheses have been reported and for trolline (3), only three. Only one total synthesis has been reported for each of the following natural products: peyoglutam (10), mescalotam (11), and the antitumor active crispine B (2). Some of the pyrrolo[2,1-a]isoquinoline alkaloids have not been synthesized yet. The following three tables summarize the synthetic efforts toward crispine A (1) (Table 1: racemic syntheses; Table 2: enantioselective syntheses) and trolline (3) (Table 3).

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 22308756     DOI: 10.1016/b978-0-12-391426-2.00002-5

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


  4 in total

1.  One-step route to tricyclic fused 1,2,3,4-tetrahydroisoquinoline systems via the Castagnoli-Cushman protocol.

Authors:  Aleksandar Pashev; Nikola Burdzhiev; Elena Stanoeva
Journal:  Beilstein J Org Chem       Date:  2020-06-24       Impact factor: 2.883

2.  Aza-Annulation of 1,2,3,4-Tetrahydro-β-carboline Derived Enaminones and Nitroenamines: Synthesis of Functionalized Indolizino[8,7-b]indoles, Pyrido[1,2-a:3,4-b']diindoles, Indolo[2,3-a]quinolizidine-4-ones and Other Tetrahydro-β-carboline Fused Heterocycles.

Authors:  Anusha Avadhani; Pethaperumal Iniyavan; Anand Acharya; Vibha Gautam; Sriparna Chakrabarti; Hiriyakkanavar Ila
Journal:  ACS Omega       Date:  2019-10-16

3.  Synthesis of pyrrolidinedione-fused hexahydropyrrolo[2,1-a]isoquinolines via three-component [3 + 2] cycloaddition followed by one-pot N-allylation and intramolecular Heck reactions.

Authors:  Xiaoming Ma; Suzhi Meng; Xiaofeng Zhang; Qiang Zhang; Shenghu Yan; Yue Zhang; Wei Zhang
Journal:  Beilstein J Org Chem       Date:  2020-06-04       Impact factor: 2.883

Review 4.  The old world salsola as a source of valuable secondary metabolites endowed with diverse pharmacological activities: a review.

Authors:  Mai H ElNaggar; Wagdy M Eldehna; Mohammed A S Abourehab; Fatma M Abdel Bar
Journal:  J Enzyme Inhib Med Chem       Date:  2022-12       Impact factor: 5.756

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.