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Intramolecular nickel catalyzed cycloadditions of bis-dienes: 3 approaches to the taxane skeleton

✍ Scribed by Paul A. Wender; Marc L. Snapper


Publisher
Elsevier Science
Year
1987
Tongue
French
Weight
255 KB
Volume
28
Category
Article
ISSN
0040-4039

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✦ Synopsis


The successful application of the nickel catalyzed, intramolecular [4+4] cycloaddition of bisdienes to the preparation of both the AB and BC ring systems of the taxane diterpenes is described. This cycloaddition methodology provides the basis for a general and efficient route to angularly alkyl-substituted bicyclo[6.4.0]dodecanes and to bicyclo[5.3.l]undecanes.


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