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- W1969394607 abstract "Abstract TeocCl (Teoc: C( O)O(CH2)2TMS) generated in situ was conveniently used for trans-protection of the N-Bn piperidine intermediate to N-Teoc piperidine. Later, deprotection of the Teoc group and the subsequent quinuclidine ring formation was achieved with CsF in a domino fashion to afford the quinine alkaloids." @default.
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- W1969394607 date "2005-09-01" @default.
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- W1969394607 title "Improved synthesis of quinine alkaloids with the Teoc protective group" @default.
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