Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5275585 | Tetrahedron Letters | 2012 | 5 Pages |
Abstract
To reach densely functionalized 1-azabicyclo[3.3.1]nonane frameworks synthesis, a stereocontrolled bridging Michael addition involving an unexplored C-5/C-6 disconnection strategy was studied. 1-Azabicyclo[3.3.1]nonane scaffolds have been diastereoselectively elaborated in fairly good yields by two concise pathways implying pyrrolidine derivative organocatalyst or enantiopure 1-phenylethylamine.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Anh Ngoc Ngo, Khadija El Kassimi, Zacharias Amara, Emmanuelle Drège, Delphine Joseph,