Реферат: A new approach was suggested for the development of new carbon-based synthons on donor-acceptor cyclopropane (DAC) basis, that are more complex than the usual cyclopropane ring, while maintaining the principle of separation of donor and acceptor substituents in the molecule. This approach is based on expansion of the reactive cyclopropane ring system in DACs by inserting into the structure the additional reactive C−C double bond or the second cyclopropane ring between donor and acceptor substituents. Within this approach and applying a set of procedures adopted in cyclopropane chemistry, the new (2-phenylcyclopropyl)methylidenemalonate (3) and related 2 ’-phenylbicyclopropyl-1,1-dicarboxylate (2) were synthesized as vinylog and homovinylog of donor-acceptor cyclopropanes. Upon studying their reactivity, focusing on their transformations in the presence of various Lewis acids, the bicyclopropyl skeleton in 2 behaved as a single six-carbon synthon, in which both cyclopropane rings reacted in tandem furnishing various products with opening of the cyclopropane rings. On the other hand, the vinylcyclopropane 3 turned out to be much less reactive towards the same Lewis acids. Mechanistic aspects, further transformations of the ring-opened products and potential synthetic applications of these new reactions in organic synthesis are being discussed as well.

Библиографическая ссылка: Denisov D.A. , Novikov R.A. , Potapov K.V. , Korolev V.A. , Shulishov E.V. , Tomilov Y.V.
1,1 ’-Bicyclopropyl-2,2-dicarboxylate and Cyclopropylmethylidenemalonate as Homovinylogs and Vinylogs of Donor-Acceptor Cyclopropanes
ChemistrySelect. 2016. V.1. N20. P.6374-6381. DOI: 10.1002/slct.201601506 WOS Scopus OpenAlex

Идентификаторы БД:

≡ Web of science:	WOS:000395432400007
≡ Scopus:	2-s2.0-85028285921
≡ OpenAlex:	W2562698242

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