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Results: 1-3 |
Results: 3
Stereoselective synthesis of gem-dimethyl-5,5-pyrrolidine-trans-lactam (5-oxo-hexahydropyrrolo[3,2-b]pyrrole)
Authors: Borthwick, AD Davies, DE Exall, AM Pennell, AMK Richards, JJ
Citation: Ad. Borthwick et al., Stereoselective synthesis of gem-dimethyl-5,5-pyrrolidine-trans-lactam (5-oxo-hexahydropyrrolo[3,2-b]pyrrole), TETRAHEDR L, 42(39), 2001, pp. 6933-6935
Stereoselective synthesis of alpha-methyl and beta-methyl pyrrolidine 5,5-trans-lactam (5-oxo-hexahydro-pyrrolo[3,2-b]pyrrole) and stereoselective alkylation of the strained pyrrolidine 5,5-trans-lactam ring system
Authors: Borthwick, AD Crame, AJ Davies, DE Exall, AM Jackson, DL Mason, AM Pennell, AMK Weingarten, GG
Citation: Ad. Borthwick et al., Stereoselective synthesis of alpha-methyl and beta-methyl pyrrolidine 5,5-trans-lactam (5-oxo-hexahydro-pyrrolo[3,2-b]pyrrole) and stereoselective alkylation of the strained pyrrolidine 5,5-trans-lactam ring system, SYNLETT, (4), 2000, pp. 504-508
Design and synthesis of pyrrolidine-5,5-trans-lactams (5-oxo-hexahydro-pyrrolo[3,2-b]pyrroles) as novel mechanism-based inhibitors of human cytomegalovirus protease. 1. The alpha-methyl-trans-lactam template
Authors: Borthwick, AD Angier, SJ Crame, AJ Exall, AM Haley, TM Hart, GJ Mason, AM Pennell, AMK Weingarten, GG
Citation: Ad. Borthwick et al., Design and synthesis of pyrrolidine-5,5-trans-lactams (5-oxo-hexahydro-pyrrolo[3,2-b]pyrroles) as novel mechanism-based inhibitors of human cytomegalovirus protease. 1. The alpha-methyl-trans-lactam template, J MED CHEM, 43(23), 2000, pp. 4452-4464
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