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- W2953372004 abstract "Alkenyldihydrooxazoles undergo a highly diastereoselective formal aza-Diels–Alder reaction with aryl and arenesulfonyl isocyanates to give oxazolo[3,2-c]pyrimidines. Depending on the substitution pattern of the alkenyldihydrooxazole, these compounds may then undergo addition of a second equivalent of the isocyanate to give either tetrahydrooxazolo[3,2-c]pyrimidine-8-carboxamides or octahydroazeto[2,3-d]oxazolo[3,2-c]pyrimidines. The second addition is sensitive to steric and electronic factors, and can be prevented in some cases." @default.
- W2953372004 created "2019-06-27" @default.
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- W2953372004 creator A5071853335 @default.
- W2953372004 date "2010-06-09" @default.
- W2953372004 modified "2023-09-26" @default.
- W2953372004 title "ChemInform Abstract: Asymmetric Hetero-Diels-Alder Reactions of Alkenyldihydrooxazoles. Synthesis of Oxazolo[3,2-c]pyrimidines and Related Compounds." @default.
- W2953372004 cites W2056565878 @default.
- W2953372004 doi "https://doi.org/10.1002/chin.200012160" @default.
- W2953372004 hasPublicationYear "2010" @default.
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