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- W2039462893 abstract "The synthesis of a new, suitably protected and activated binaphthalene building block representing the central structural element of all known natural dimeric naphthylisoquinoline alkaloids, is described. This functionalized fragment possesses organometallically robust O-isopropyl (instead of O-acetyl) protecting groups and bromo (instead of trifluoromethanesulfonyloxy) activation at the scheduled coupling positions. Starting from a biphenyl intermediate, the construction of the two `outer' naphthalene rings has been achieved by a Wittig reaction → cyclization sequence." @default.
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- W2039462893 date "2000-01-01" @default.
- W2039462893 modified "2023-09-24" @default.
- W2039462893 title "A New Central Binaphthalene Building Block for Michellamine Syntheses" @default.
- W2039462893 doi "https://doi.org/10.1055/s-2000-6340" @default.
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