One-pot cascade synthesis of fused nitrogen-containing heterocycles in aqueous media - utility of n -protective groups in ıntramolecular diels-alder reaction of furan
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Tarih
2016
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Georg Thieme Verlag
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
A metal-free, thermal, intramolecular Diels-Alder (IMDA) reaction of furan in aqueous media without the use of microwave irradiation was investigated. Protection of the amine functionality and the cycloaddition reaction were performed as a one-pot, two-component process. Various nitrogen-protecting groups and their electronic and steric effects on the cycloaddition reaction were studied. The protection-intramolecular Diels-Alder reaction sequence proceeds under environmentally benign aqueous conditions, which are tolerated by substrates with a broad range of nitrogen-protecting groups such as benzyloxycarbonyl (Cbz), trityl, tert-butoxycarbonyl (Boc), trifluoroacetyl, tosyl, mesyl, and p-nosyl [(4-nitrophenyl)sulfonyl]. This study allowed the development of a stereoselective, tandem allylamine isomerization-Diels-Alder cycloaddition sequence leading to the rapid assembly of complex nitrogen-containing heterocycles in a simple one-pot process.
Açıklama
Anahtar Kelimeler
Cycloaddition, Cascade Reactions, Intramolecular Diels-Alder Reaction, Heterocycles, Furan
Kaynak
SYNTHESIS-STUTTGART
WoS Q Değeri
N/A
Scopus Q Değeri
Q2
Cilt
48
Sayı
17
