Unknown

Dataset Information

0

Synthesis of the tetracyclic core of Illicium sesquiterpenes using an organocatalyzed asymmetric Robinson annulation.


ABSTRACT: An enantioselective synthesis of the core framework of neurotrophic Illicium majucin-type sesquiterpenes is described here. This strategy is based on an organocatalyzed asymmetric Robinson annulation and provides an efficient approach for a diversity-oriented synthesis of Illicium natural products that holds remarkable therapeutic potential for neurodegenerative diseases.

SUBMITTER: Trzoss L 

PROVIDER: S-EPMC3701413 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

altmetric image

Publications

Synthesis of the tetracyclic core of Illicium sesquiterpenes using an organocatalyzed asymmetric Robinson annulation.

Trzoss Lynnie L   Xu Jing J   Lacoske Michelle H MH   Theodorakis Emmanuel A EA  

Beilstein journal of organic chemistry 20130612


An enantioselective synthesis of the core framework of neurotrophic Illicium majucin-type sesquiterpenes is described here. This strategy is based on an organocatalyzed asymmetric Robinson annulation and provides an efficient approach for a diversity-oriented synthesis of Illicium natural products that holds remarkable therapeutic potential for neurodegenerative diseases. ...[more]

Similar Datasets

| S-EPMC5261859 | biostudies-literature
| S-EPMC3946388 | biostudies-literature
| S-EPMC3489503 | biostudies-other
| S-EPMC2771404 | biostudies-literature
| S-EPMC3875175 | biostudies-literature
| S-EPMC2720047 | biostudies-literature
| S-EPMC2527759 | biostudies-literature