@article{comins_fulp_2001, title={Enantiopure 2,3-dihydro-4-pyridones as synthetic intermediates: asymmetric synthesis of 1-deoxynojirimycin}, volume={42}, ISSN={["0040-4039"]}, DOI={10.1016/S0040-4039(01)01432-0}, abstractNote={An asymmetric synthesis of 1-deoxynojirimycin (2) mediated by a chiral auxiliary is reported. The dihydropyridone 4 was converted to diol 11 in three steps by acetoxylation, hydrolysis, and stereoselective reduction. Dihydroxylation of 11 followed by catalytic reduction afforded 2.}, number={39}, journal={TETRAHEDRON LETTERS}, author={Comins, DL and Fulp, AB}, year={2001}, month={Sep}, pages={6839–6841} }
 @article{comins_fulp_1999, title={Enantiopure N-acyldihydropyridones as synthetic intermediates: Asymmetric synthesis of (-)-slaframine}, volume={1}, ISSN={["1523-7060"]}, DOI={10.1021/ol991083v}, abstractNote={[formula: see text] An asymmetric synthesis of (-)-slaframine and N-acetylslaframine has been accomplished starting from an enantiopure dihydropyridone building block. The oxygen-carbon bond at C-1 was incorporated with complete stereoselectivity by using an efficient phenylselenocyclocarbamation reaction.}, number={12}, journal={ORGANIC LETTERS}, author={Comins, DL and Fulp, AB}, year={1999}, month={Dec}, pages={1941–1943} }