
handle: 11336/68831 , 10533/132744 , 10533/132745
Alternative total syntheses of (―)-lupinine (1) and (―)-epiquinamide (2) have been described via the key intennediate 3 obtained from the addition of 2-trialkylsilyloxyfuran 5 to N-acyliminium intermediate derived from 4. The major R,R-isomer 8 obtained from the Mannich reaction was converted into its R,S-isomer through Mitsunobu reaction. Then, a second Mitsunobu reaction of 3 led to cyano 9 and azido 11 derivatives, which were converted into 1 and 2 in 33 and 36% overall yield from 4, respectively. The synthetic route is amenable for the generation of several quinolizidine alkaloids.
quinolizidine alkaloids, Quinolizidine Alkaloids, azido reduction, nickel boride, Microwave Irradiation, Nickel Boride, Mitsunobu reaction, Azido Reduction, Mitsunobu Reaction, https://purl.org/becyt/ford/1.4, https://purl.org/becyt/ford/1, microwave irradiation
quinolizidine alkaloids, Quinolizidine Alkaloids, azido reduction, nickel boride, Microwave Irradiation, Nickel Boride, Mitsunobu reaction, Azido Reduction, Mitsunobu Reaction, https://purl.org/becyt/ford/1.4, https://purl.org/becyt/ford/1, microwave irradiation
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