Total synthesis of lamellarin G trimethyl ether through enaminone cyclocondensation-Reference-Cited by-同舟云学术

Total synthesis of lamellarin G trimethyl ether through enaminone cyclocondensation

Published:2023 Issue:29 Volume:21 Page:5997-6007
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Šachlevičiūtė Urtė¹²^ORCID,Kleizienė Neringa¹^ORCID,Bieliauskas Aurimas¹^ORCID,Šačkus Algirdas¹,Opatz Till²^ORCID

Affiliation:

1. Institute of Synthetic Chemistry, Kaunas University of Technology, K. Baršausko g. 59, LT-51423 Kaunas, Lithuania

2. Department of Chemistry, Johannes Gutenberg University Mainz, Duesbergweg 10-14, 55128 Mainz, Germany

Abstract

A synthesis of pyrrolo[2,1-a]isoquinolines based on intramolecular condensation of an enaminone intermediate obtained by C-acylation of an N-alkylated 6,7-dimethoxy-1-methyl-3,4-dihydroisoquinolinium salt was developed.

Funder

Directorate-General XII, Science, Research, and Development

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00870C

Reference53 articles.

1. Metabolites of the marine prosobranch mollusk Lamellaria sp

2. Anticancer Properties of Lamellarins

3. Lamellarin alkaloids: Isolation, synthesis, and biological activity

4. Synthetic Approaches to the Lamellarins—A Comprehensive Review

5. Recent progress in the synthesis of pyrrolo[2,1-a]isoquinolines

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2. Chromenone‐Fused Pyrrolizines and Pyrrolizine Analogues of Lamellarins: Expanding the Lamellarin Family;European Journal of Organic Chemistry;2024-01-23

3. Recent advances in the synthesis of chromenone fused pyrrolo[2,1-a]isoquinoline derivatives;New Journal of Chemistry;2023