Efficient enantiomeric synthesis of pyrrolidine and piperidine alkaloids from tobacco

An enantiomeric synthesis of six piperidine and pyrrolidine alkaloids, (S)- nornicotine 1, (S)-nicotine 2, (S)-anatabine 3, (S)-N-methylanatabine 4, (S )-anabasine 5, and (S)-N-methylanabasine 6, known as natural products in to bacco, was established from a common chiral homoallylic (S)-3-azido-but-3-e nyl)-pyridine 15. An intramolecular hydroboration-cycloalkylation of the ho moallylic azide intermediate 15 served as the key step in the pyrrolidine r ing formation. A ring closing metathesis reaction (RCM) of a diethylenic am ine intermediate (S)-allyl-(l-pyridin-3-yl-but-3-enyl)-carbamic acid benzyl ester 20 served as the key step in the piperidine ring formation. From the commercially available 3-pyridinecarboxaldehyde 13, a short and convenient enantiomeric synthesis of tobacco alkaloids is described: (S)-nornicotine 1 (5 steps, with an overall yield of 70%), (S)-nicotine 2 (6 steps, 65%), ( S)-anatabine 3 (8 steps, 30%), (S)-N-methylanatabine 4 (8 steps, 25%), (S)- anabasine 5 (8 steps, 35%), and (S)-N-methylanabasine 6 (8 steps, 25%).