The first synthesis of 6-phenyl-2,6-diazabicyclo[3.2.0]heptane 1 and its orthogonally protected precursor 2 is herein reported. Our strategy enables to chemically address the two nitrogen atoms of 2,6-diazabicyclo[3.2.0]heptane core individually and selectively, thus allowing rapid access to several subsets of widely substituted fused azetidines. (C) 2009 Elsevier Ltd. All rights reserved.

First synthesis of 2,6-diazabicyclo[3.2.0]heptane derivatives

NAPOLITANO, Carmela
Primo
;
MANFREDINI, Stefano
Ultimo
2009

Abstract

The first synthesis of 6-phenyl-2,6-diazabicyclo[3.2.0]heptane 1 and its orthogonally protected precursor 2 is herein reported. Our strategy enables to chemically address the two nitrogen atoms of 2,6-diazabicyclo[3.2.0]heptane core individually and selectively, thus allowing rapid access to several subsets of widely substituted fused azetidines. (C) 2009 Elsevier Ltd. All rights reserved.
2009
Napolitano, Carmela; Borriello, M.; Cardullo, F.; Donati, D.; Paio, A.; Manfredini, Stefano
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1389735
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