The enantioselective total synthesis of laurendecumallene B
C. Taylor, Yu‐An Zhang, Scott A. Snyder
Abstract
Br) in non-conventional solvents is essential in generating much of the target's complexity in optimal yields and stereoselectivity. Moreover, the final structural assignment of laurendecumallene B reveals that it has one element of bromine-based chirality that, to the best of our knowledge, is not shared with any other member of the class.
Topics & Concepts
Enantioselective synthesisTotal synthesisStereochemistryChemistryOrganic chemistryCatalysisChemical synthesis and alkaloidsSynthetic Organic Chemistry MethodsMarine Sponges and Natural Products