Stereoselective Synthesis of (R)-all-trans-13,14-Dihydroretinol and -Retinoic Acid
Year: 2025
Type: article
Abstract: High Resolution Image Download MS PowerPoint Slide Vitamin A (or all- trans -retinol) metabolites are involved in a wide range of cellular processes. However, the investigation of their biological role is hampered due to their very limited availability. Herein we report a stereoselective total synthesis of the vitamin A metabolites ( R )-all- trans -13,14-dihydroretinol and -retinoic acid, applying an E -selective HWE olefination and a Ru(II) catalyzed intramolecular 7- endo - dig hydrosilylation as the key steps.
Source: The Journal of Organic Chemistry
Authors: Paul Wienecke, Adriaan J. Minnaard
Institution: University of Groningen
Language: Russian
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
OpenAlex ID: W4407762017
