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Strained to the Limit: When a Cyclobutyl Moiety Becomes a Thermodynamic Sink in a Protolytic Ring Opening of Photogenerated Oxetanes

[Image: see text] Strained polycyclic oxetanes generated photochemically from the Diels-Alder adducts of cyclic dienes and enones undergo deep skeletal rearrangements under protolytic ring-opening conditions offering expeditious access to chlorohydrins and other products of unique skeletal topology.

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Detaylı Bibliyografya
Asıl Yazarlar: Valiulin, Roman A., Arisco, Teresa M., Kutateladze, Andrei G.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2010
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2912957/
https://ncbi.nlm.nih.gov/pubmed/20608636
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol101297b
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