Tetrahedron p. 10629 - 10642 (1993)
Update date:2022-09-26
Topics:
Occhiato, Ernesto G.
Guarna, Antonio
Spinetti, Laura Michela
(3S,7S,8aS)-3-Methyl-7-hydroxyoctahydroindolizine (13) was prepared with an enantiomeric excess of 74percent, in five steps starting from enantiomerically pure (S)-(+)-5-nitro-2-pentanol (5). (3S,5S,7S,8aS)-(-)-3-Methyl-5-phenyl-7-hydroxyoctahydroindolizi
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Doi:10.1016/j.bbagen.2016.03.032
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(1994)Doi:10.1016/0040-4039(94)88177-4
(1994)
