A highly flexible route to tricyclo[4.3.1.03.7]-, and tricyclo[4.3.0.04,10]decanes A short synthesis of pupukean-2-one
β Scribed by P. John Biju; G.S.R. Subba Rao
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 174 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
An efficient strategy for the construction of and tricyclo[4.3.0.O4'lΒ°]decanes is described which involves a novel one-pot tandem acid-catalyzed rearrangement followed by an ene cyclization as key step and is exemplified by the total synthesis of pupukean-2-one 3.
π SIMILAR VOLUMES
In a recent communication (11, Schleyer and Aiskott pointed out that of the conceivable tricyclononanes only four (I-IV) do not possess three or four-membered rings or highly strained skeletons. Brendane (I), brexane (II) and noradamantane (III) are known (2). Be now wish to report the synthesis of
THE SYNTHESIS OF EXO EXO-ll-OXATETRACYCLO[4.4.l.O.2,507,1o]"~DECA-3,8-DIENE. THE -,-STEREOCHEMISTRY OF THE TRICYCL0:6.2.0.0 3,6]DECANE DERIVATIVE OBTAINED BY THE
Furthsr studies of ionizations of endo-bicyclo[2.l.O]pent-2-yl msnts on the nature of the various transition states involved: