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Reaktsiya Prinsa yavlyaetsya udobnym metodom polucheniya kislorodsoderzhashchikh geterotsiklov. V proshlom veke osoboe vnimanie udelyalos' sintezu 1,3-dioksanov. Nachalo 21 stoletiya otmecheno rostom interesa k sintezam gidrirovannykh piranov i furanov po tak nazyvaemoy tsiklizatsii po Prinsu i eye modifikatsiyami (silil-Prins, aza-Prins, aza-silil-Prins). V rabote rassmotreny sovremennye predstavleniya o mekhanizme reaktsii Prinsa. Predlozhennaya Praysom skhema prevrashcheniy korrektno opisyvaet obrazovanie lineynykh produktov reaktsii 1,3-diolov i nenasyshchennykh spirtov. Obrazovanie 1,3-dioksanov ne mozhet byt' opisano etoy skhemoy i protekaet s uchastiem oligomerov formal'degida. Vtorichnye produkty reaktsii Prinsa, takie kak gidrirovannye pirany i furany, obrazuyutsya v rezul'tate vnutrimolekulyarnoy tsiklizatsii sootvetstvuyushchikh nenasyshchennykh spirtov. Faktorom, opredelyayushchim kharakter produktov reaktsii Prinsa, yavlyaetsya vnutri- ili mezhmolekulyarnyy tip stabilizatsii karbokationa, obrazuyushchegosya pri atake alkena protonirovannoy molekuloy karbonil'nogo soedineniya. Monografiya mozhet byt' poleznoy dlya spetsialistov zanimayushchikhsya issledovaniyami v oblasti geterotsiklicheskikh soedineniy, a takzhe dlya studentov, magistrantov i aspirantov.