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Journals and Conferences
The marine macrolide bryostatin 7 is prepared in 20 steps (longest linear sequence) and 36 total steps with five C-C bonds formed using hydrogenative methods. This approach represents the most… (More)
The total synthesis of (-)-amphidinolide E was accomplished by following a synthetic scheme that incorporates the labile C2 stereocenter at a very late stage. The oxolane unit was prepared by… (More)
Correction for 'One-pot synthesis of carbazoles via tandem C-C cross-coupling and reductive amination' by Deuk-Young Goo, et al., Org. Biomol. Chem., 2016, DOI: 10.1039/c5ob01952d.
A method for [3 + 2] cycloaddition of oxaziridines with alkynes to form 4-isoxazolines via visible-light photoredox catalysis is described. This method is a greener, atom-economical reaction that… (More)
The canonical SN 2 behavior displayed by alcohols and activated alkyl halides in basic media (O-alkylation) is superseded by a pathway leading to carbinol C-alkylation under the conditions of… (More)
An intramolecular Prins macrocyclization reaction was successfully employed in the synthesis of polycavernoside A.
The 14-membered macrolide 6-deoxyerythronolide B is prepared in 14 steps (longest linear sequence) and 20 total steps. Two different methods for alcohol CH-crotylation via transfer hydrogenation are… (More)