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Attachment of the anthramycin acrylamide side chain by the palladium catalyzed coupling reaction of a vinyl triflate

✍ Scribed by Michael R. Peña; J.K. Stille


Book ID
104228211
Publisher
Elsevier Science
Year
1987
Tongue
French
Weight
188 KB
Volume
28
Category
Article
ISSN
0040-4039

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✦ Synopsis


Conversion of the 2-keto group in the pyrrolo ring of pyrrolo(l,4)benzodiazepines to the vinyl triflate takes place regiospecifically to yield the enamine.

The triflate undergoes palladium catalyzed coupling reactions to attach the acrylamide side chain.


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