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• W4313260045 endingPage "182" @default.
• W4313260045 startingPage "182" @default.
• W4313260045 abstract "Herein, we present a mild strategy for deprotecting cyclic sulfamidates via the Kukhtin–Ramirez reaction to access amino sugars. The method features the removal of the sulfonic group of cyclic sulfamidates, which occurs through an N-H insertion reaction that implicates the Kukhtin–Ramirez adducts, followed by a base-promoted reductive N-S bond cleavage. The mild reaction conditions of the protocol enable the formation of amino alcohols including analogs that bear multiple functional groups." @default.
• W4313260045 created "2023-01-06" @default.
• W4313260045 creator A5013522067 @default.
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• W4313260045 creator A5045578484 @default.
• W4313260045 creator A5055145708 @default.
• W4313260045 creator A5083940144 @default.
• W4313260045 date "2022-12-25" @default.
• W4313260045 modified "2023-10-14" @default.
• W4313260045 title "Kukhtin–Ramirez-Reaction-Inspired Deprotection of Sulfamidates for the Synthesis of Amino Sugars" @default.
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• W4313260045 doi "https://doi.org/10.3390/molecules28010182" @default.
• W4313260045 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36615376" @default.
• W4313260045 hasPublicationYear "2022" @default.
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