Synthetic Approaches To Construct the 6,8-DOBCO Framework in Natural Products
1Department of Chemistry, The Hong Kong University of Science and Technology , Clearwater Bay, Kowloon, Hong Kong, China.
Abstract:
6,8-Dioxabicyclo[3.2.1]octane skeleton (6,8-DOBCO) is a very common structural motif in many biologically active natural products. This synopsis surveys various approaches used to access the 6,8-DOBCO framework present in natural products and summarizes total syntheses of 6,8-DOBCO-containing psoracorylifol B, ent-psoracorylifol C, didemniserinolipid B, and attenol B from our laboratory and others.
Related Concept Videos
Diels–Alder Reaction Forming Cyclic Products: Stereochemistry
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
Cycloaddition Reactions: Overview
Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism
Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation


![Solid-phase Synthesis of [4.4] Spirocyclic Oximes](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F58508.jpg&w=3840&q=50)