## one (25) and their ethylene acetals 24 and 26, respectively, were derived from the Diels-Alder adduct of furan to I-cyanovinyl acetate (27). The Diels-Alder additions of 26 to dimethyl acetylenedicarboxylate, to methyl propynoate, to N-phenylmaleimide, and to methyl acrylate were highly exo-fac
Homochiral matching in the Diels-Alder cyclodimerization of 2-vinyl-7-oxabicyclo[2.2.1]hept-2-ene derivatives
β Scribed by Lieven Meerpoel; Maria-Miranda Vrahami; Jacek Ancerewicz; Pierre Vogel
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 339 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
Dedicated to Prof. Ch. Tamm on the occasion of his 60th birthday (12.4.83) ## Summary (-)-1-Camphanoyloxyacrylonitrile (= (-)-1 -cyanovinyl camphanate; 1) obtained from the commercially available ( -)-camphanoyl chloride and 2-0x0propiononitrile added to furan at 20" in the presence of CU(BF,)~.
## Abstract A new, practical method for the optical resolution of bicyclic ketones if illusttrated by the preparation of (+)β(1__R__,4__R__)β7βoxabicyclo[2.2.1]beptβ5βenβ2βone ((+)β**1**) and (+)β(1__R__, 2__S__,4__R__)β2βcyanoβ7βoxabicyclo[2.2.1]heptβ5βenβ2βyul acetate ((+)β**4**). It involves the
The I-dimethoxymethyl-5,6-dimethylidene-7-oxabicyclo[2.2. I jhept-2-ene (9) has been prepared. On treatment with Fe,(CO),, the endocyclic double bond C(2)=C(3) was coordinated first giving the Corresponding exo-Fe(C0)4 complex 10. The latter reacted with Fe,(CO), and afforded cis-heptacarbonyl-p -[(