Synthesis and reactions of sulfur-substituted indolizidinones

An aza-Diels–Alder reaction product 2 was readily converted to a tetrahydropyridine derivative 6, but its N-benzyl group was unexpectedly difficult to cleave under various conditions. On the other hand, the N-tosyl α,β-unsaturated ester 14 was transformed in one step by Mg/MeOH/Et3N to a thio-substituted indolizidinone 3. This method was also extended to a methyl-substituted diene 16, which stereoselectively provided the cis-2,6-disubstitutedproduct 17. Further synthetic transformations yielded indolizidinones 20–24, including a formal synthesis of the natural product monomorine I.

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