About: New Routes to N-Alkylated Cyclic Sulfamidates

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_15/w
Subject	Article
Title	New Routes to N-Alkylated Cyclic Sulfamidates
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_15/101021jo0157019/m/print http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_15/101021jo0157019/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_15/101021jo0157019/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_15/101021jo0157019/authorship/3 http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_15/101021jo0157019/authorship/1
Author	Posakony Jeffrey J. Grierson John R. Tewson Timothy J.
Abstract	BOC- and dibenzosuberyl-protected chiral and hindered cyclic sulfamidates ([1,2,3]-oxathiazolidine-2,2-dioxides) were synthesized and subsequently deprotected using trifluoroacetic acid. The resultingcrystalline sulfamidates were then used in several alkylation reactions involving benzyl bromideand alcohols in a versatile route to cyclic sulfamidates with differing N-alkyl substituents.
article type	research-article
is part of this journal	The Journal of Organic Chemistry

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