Diastereoselective routes to endo and exo ethyl 1-azabicyclo[2.2.1] hept-3-YL carboxylates
Cheminform(1991)
摘要
Diastereoselective routes to endo and exo ethyl 1-azabicyclo[2.2.1]hept-3-yl-carboxylates (1) and (2) based on the hydrogen bromide cleavage of the isomeric [4.3.0] bicyclic cis fused lactones (3) and (4) are described.
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关键词
cheminform abstract,diastereoselective routes,exo-ethyl
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