Total synthesis of kealiiquinone: the regio-controlled strategy for accessing its 1-methyl-4-arylbenzimidazolone core-Reference-Cited by-同舟云学术

Total synthesis of kealiiquinone: the regio-controlled strategy for accessing its 1-methyl-4-arylbenzimidazolone core

Published:2018 Issue:54 Volume:8 Page:30761-30776
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Ramadoss Velayudham¹²³⁴⁵^ORCID,Alonso-Castro Angel J.¹⁶³⁵⁷^ORCID,Campos-Xolalpa Nimsi⁸⁹¹⁰⁷^ORCID,Ortiz-Alvarado Rafael¹¹¹²¹³⁷^ORCID,Yahuaca-Juárez Berenice¹¹¹²¹³⁷^ORCID,Solorio-Alvarado César R.¹²³⁴⁵^ORCID

Affiliation:

1. Universidad de Guanajuato

2. Departamento de Química

3. División de Ciencias Naturales y Exactas

4. Campus Guanajuato

5. Guanajuato

6. Departamento de Farmacia

7. Mexico

8. Universidad Metropolitana

9. Unidad Xochimilco

10. México D.F.

11. Universidad Michoacana de San Nicolás de Hidalgo

12. Facultad de Químico Farmacobiología

13. Morelia

Abstract

A practical, concise and straightforward total synthesis of kealiiquinone 1, a naphtho[2,3-d]imidazole alkaloid obtained from the Micronesian marine sponge Leucetta sp. was accomplished.

Funder

Consejo Nacional de Ciencia y Tecnología

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/RA/C8RA06676K

Reference39 articles.

1. Bioactive Natural Products of Marine Sponges from the Genus Hyrtios

2. New Imidazole Alkaloids From the Sponge Leucetta sp. and the Associated Predatory Nudibranch Notodoris gardineri

3. Total Synthesis of (−)-Spiroleucettadine