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, CarmelaPrimo
;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.File in questo prodotto:
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