Synthesis 2017; 49(03): 532-538
DOI: 10.1055/s-0036-1588629
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© Georg Thieme Verlag Stuttgart · New York

Stereoselective Multibond-Forming Process towards Functionalized Sulfamide-Containing Polycycles

Loïc Pantaine
Institut Lavoisier de Versailles, UMR CNRS 8180, Université de Versailles Saint-Quentin-en-Yvelines, 45 Avenue des États-Unis, 78035 Versailles cedex, France   Email: vincent.coeffard@uvsq.fr   Email: christine.greck@uvsq.fr
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Aragorn Laverny
Institut Lavoisier de Versailles, UMR CNRS 8180, Université de Versailles Saint-Quentin-en-Yvelines, 45 Avenue des États-Unis, 78035 Versailles cedex, France   Email: vincent.coeffard@uvsq.fr   Email: christine.greck@uvsq.fr
,
Xavier Moreau
Institut Lavoisier de Versailles, UMR CNRS 8180, Université de Versailles Saint-Quentin-en-Yvelines, 45 Avenue des États-Unis, 78035 Versailles cedex, France   Email: vincent.coeffard@uvsq.fr   Email: christine.greck@uvsq.fr
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Vincent Coeffard*
Institut Lavoisier de Versailles, UMR CNRS 8180, Université de Versailles Saint-Quentin-en-Yvelines, 45 Avenue des États-Unis, 78035 Versailles cedex, France   Email: vincent.coeffard@uvsq.fr   Email: christine.greck@uvsq.fr
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Christine Greck*
Institut Lavoisier de Versailles, UMR CNRS 8180, Université de Versailles Saint-Quentin-en-Yvelines, 45 Avenue des États-Unis, 78035 Versailles cedex, France   Email: vincent.coeffard@uvsq.fr   Email: christine.greck@uvsq.fr
› Author Affiliations
Further Information

Publication History

Received: 15 September 2016

Accepted after revision: 29 September 2016

Publication Date:
15 November 2016 (eFirst)

Abstract

Original polycyclic-containing sulfamide compounds have been synthesized through a domino aza-Michael/Michael/aldol condensation sequence. Resolution of the racemic bicyclic sulfamide starting materials to provide enantioenriched structures has also been investigated.

Supporting Information

 
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