ISSN:
0947-3440
Keywords:
Medium-sized rings
;
Alkynes
;
Conformation analysis
;
Ketones
;
Cyclizations
;
Ether
;
Chemistry
;
Organic Chemistry
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
The following 14-membered ring diynes have been synthesized: cyclotetradeca-4,11-diynone (4), cyclotetradeca-4,11-diyne-1,8-dione (6), the corresponding exomethylene derivatives 5 and 7, as well as 1,8-dioxacyclotetradeca-4,11-diyne (8). The synthesis of the diketal of 4 was achieved by the reaction of the ethylene ketal of 1,5-dibromopentan-3-one (9) with the dilithium salt of 1,8-nonadiyne. Similarly, the diketal of 6 was prepared from the dilithium salt of the ethylene ketal of 1,8-nonadiyn-5-one 11 with 9. The unprotected ketones 4 and 6 were obtained by treating the ketals 10 and 14, respectively, with HCl. The ketones 4 and 6 were transformed to the exomethylene derivatives by a Wittig reaction. The reaction of the dilithium salt of 5-oxanona-1,8-diyne (16a) with 1,5-dibromo-3-oxapentane (15) yielded 8. X-ray investigations of single crystals of 6 and 8 revealed chair conformations with a zig-zag arrangement, employing two anti orientations of the two chains between the triple bonds. A zig-zag arrangement of the chain containing the carbonyl group was also found in 4. In 3b and 7 Ci symmetry was found, with only one anti conformation in each chain. Molecule 6 crystallizes with C2h symmetry and 8 with a center of symmetry.
Additional Material:
2 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/jlac.199719970734
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