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    Cobryketone Derived from Vitamin B<sub>12</sub> <i>via</i> Palladium-Catalyzed Cleavage of the sp<sup>3</sup>ā€“sp<sup>3</sup> Carbonā€“Carbon Bond

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    Heptamethyl cobyrinate was transformed into hexamethyl 8-<i>nor</i>-cobyrinate. The crucial step involved the synthesis of new, vitamin B<sub>12</sub> derived cobryketone <i>via</i> palladium-catalyzed cleavage of the sp<sup>3</sup>ā€“sp<sup>3</sup> carbonā€“carbon bond with the liberation of the ketone. The replacement of sp<sup>3</sup> carbon atom with sp<sup>2</sup> (Cī—»O) at the 8-position produces a bathochromic shift of all absorption bands and makes Ī± and Ī² bands equal as a consequence of the expansion of the existing conjugated system of double bonds
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