COMPOUNDS WITH BRIDGEHEAD NITROGEN - PART 76 - THE STEREOCHEMISTRY OFPERHYDROCYCLOHEPTA[F]PYRIDO[1,2-C][1,3]OXAZEPINES AND CYCLOOCTA[F]PYRIDO[1,2-C][1,3]OXAZEPINES
Ta. Crabb et al., COMPOUNDS WITH BRIDGEHEAD NITROGEN - PART 76 - THE STEREOCHEMISTRY OFPERHYDROCYCLOHEPTA[F]PYRIDO[1,2-C][1,3]OXAZEPINES AND CYCLOOCTA[F]PYRIDO[1,2-C][1,3]OXAZEPINES, ACH, models in chemistry, 135(4), 1998, pp. 485-491
Whereas syn-perhydrocyclohepta- and cycloocta[f]pyrido[1,2-c][1,3]oxaz
epine preferentially adopt the trans-syn-trans- conformations (ca. 92
and 90 %, respectively, in CD2Cl2 at 183 K) the corresponding anti-iso
mers prefer the cis-anti-trans-conformations (ca. 90 % and 75 %, respe
ctively, in CD2Cl2 at 183 K).