Unknown

Dataset Information

0

Synthesis of a tyrosinase inhibitor by consecutive ethenolysis and cross-metathesis of crude cashew nutshell liquid.


ABSTRACT: A convenient and sustainable three-step synthesis of the tyrosinase inhibitor 2-hydroxy-6-tridecylbenzoic acid was developed that starts directly from the anacardic acid component of natural cashew nutshell liquid (CNSL). Natural CNSL contains 60-70% of anacardic acid as a mixture of several double bond isomers. The anacardic acid component was converted into a uniform starting material by ethenolysis of the entire mixture and subsequent selective precipitation of 6-(ω-nonenyl)salicylic acid from cold pentane. The olefinic side chain of this intermediate was elongated by its cross-metathesis with 1-hexene using a first generation Hoveyda-Grubbs catalyst, which was reused as precatalyst in a subsequent hydrogenation step. Overall, the target compound was obtained in an overall yield of 61% based on the unsaturated anacardic acid content and 34% based on the crude CNSL.

SUBMITTER: Pollini J 

PROVIDER: S-EPMC6244364 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature

altmetric image

Publications

Synthesis of a tyrosinase inhibitor by consecutive ethenolysis and cross-metathesis of crude cashew nutshell liquid.

Pollini Jacqueline J   Bragoni Valentina V   Gooßen Lukas J LJ  

Beilstein journal of organic chemistry 20181031


A convenient and sustainable three-step synthesis of the tyrosinase inhibitor 2-hydroxy-6-tridecylbenzoic acid was developed that starts directly from the anacardic acid component of natural cashew nutshell liquid (CNSL). Natural CNSL contains 60-70% of anacardic acid as a mixture of several double bond isomers. The anacardic acid component was converted into a uniform starting material by ethenolysis of the entire mixture and subsequent selective precipitation of 6-(ω-nonenyl)salicylic acid fro  ...[more]

Similar Datasets

| S-EPMC11357457 | biostudies-literature
| S-EPMC3104465 | biostudies-literature
| S-EPMC3667417 | biostudies-literature
| S-EPMC4618480 | biostudies-literature
| S-EPMC11618440 | biostudies-literature
| S-EPMC3561906 | biostudies-literature
| S-EPMC6381869 | biostudies-literature
| S-EPMC6767058 | biostudies-literature
| S-EPMC8466601 | biostudies-literature
| S-EPMC8348646 | biostudies-literature