4.8 Article

Access to Naphthoic Acid Derivatives through an Oxabenzonorbornadiene Rearrangement

Journal

ORGANIC LETTERS
Volume 25, Issue 40, Pages 7349-7353

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.3c02823

Keywords

-

Ask authors/readers for more resources

Here, a synthesis method of 1-hydroxy-2-naphthoic acid esters through an unexpected Lewis-acid-mediated 1,2-acyl shift of oxabenzonorbornadienes is reported. This method allows the obtaining of novel substitution patterns for 1-hydroxy-2-naphtoic acid esters. A mechanistic proposal and rationale for this transformation, which had been previously incorrectly characterized, is provided.
Herein, the synthesis of 1-hydroxy-2-naphthoic acid esters through an unexpected Lewis-acid-mediated 1,2-acyl shift of oxabenzonorbornadienes is reported. Using this methodology, novel substitution patterns for 1-hydroxy-2-naphtoic acid esters can be obtained. A mechanistic proposal and rationale for this transformation, the products of which had been previously incorrectly characterized, is given.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available