Diastereoselective routes to endo and exo ethyl 1-azabicyclo [2.2. 1] hept-3-YL carboxylates
BS Orlek, H Wadsworth, P Wyman, MS Hadley
Index: Orlek, Barry S.; Wadsworth, Harry; Wyman, Paul; Hadley, Michael S. Tetrahedron Letters, 1991 , vol. 32, # 9 p. 1241 - 1244
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Citation Number: 14
Abstract
Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Diastereoselective routes to and 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 fused lactones (3) and (4) are described. ... The and azabicyclic esters (1) and (2) are obtained by rearrangement of the ...
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