Intermolecular [4 + 2] process of N-acyliminium ions with simple olefins for construction of functional substituted-1,3-oxazinan-2-ones
An efficient approach to functionalized 4,6-disubstituted-and 4,6,6-trisubstituted-1,3-oxazinan-2-ones skeleton has been developed through the reaction of semicyclic N,O-acetals 4a and 4b with 1,1-disubstituted ethylenes 5 or 8. As a result of such a [4 + 2] cycloaddition process, 4,6,6-trisubstitut...
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Published in | Chinese chemical letters Vol. 32; no. 11; pp. 3526 - 3530 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
NEW YORK
Elsevier B.V
01.11.2021
Elsevier Institutes of Biomedical Sciences and School of Pharmacy,Fudan University,Shanghai 200433,China%Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China |
Subjects | |
Online Access | Get full text |
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Summary: | An efficient approach to functionalized 4,6-disubstituted-and 4,6,6-trisubstituted-1,3-oxazinan-2-ones skeleton has been developed through the reaction of semicyclic N,O-acetals 4a and 4b with 1,1-disubstituted ethylenes 5 or 8. As a result of such a [4 + 2] cycloaddition process, 4,6,6-trisubstituted-1,3-oxazinan-2-ones 6aa, 6af-6au, 7ba, 7bf-7bw and 6,6-spiro containing 1,3-oxazinan-2-ones 9ad, 9ae, 10ba-10bg were obtained in 36%-96% yields and with moderate to excellent diastereoselectivities. In addition, the synthesis of (±)-norallosedamine 12 could be conveniently achieved from the cycloadduct 7bf.
An efficient approach to functionalized 4,6-disubstituted-and 4,6,6-trisubstituted-1,3-oxazinan-2-ones skeletons has been developed through the reaction of semicyclic N,O-acetals with 1,1-disubstituted ethylenes. [Display omitted] |
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ISSN: | 1001-8417 1878-5964 |
DOI: | 10.1016/j.cclet.2021.05.003 |