Studies on organometallic compounds. VII. Reaction of di-tert-butyl dicarbonate with α-trialkylstannyl derivatives of pyridine, quinoline, and isoquinoline

Article abstract of DOI:10.1248/cpb.43.916

Di-tert-butyl dicarbonate was found to be effective for direct introduction of a tert-butoxycarbonyl group at the α-position of the pyridine nucleus via the trialkylstannyl group; reaction of α-trialkylstannyl derivatives of pyridine, quinoline, and isoquinoline with di-tert-butyl dicarbonate gave the corresponding α-tert-butoxycarbonyl derivatives in good yields, although small amounts of a variety of by-products were formed except in the case of pyridine.

Full text of DOI:10.1248/cpb.43.916

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