129222-15-7Relevant academic research and scientific papers
DERIVATIVES OF AZABICYCLO OCTANE, THE METHOD OF MAKING THEM AND THE USES THEREOF AS INHIBITORS OF DIPEPTIDYL PEPTIDASE IV
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Page/Page column 19-20, (2009/12/27)
Derivatives of azabicyclo octane presented by formula (I), the method of making them, and the compositions containing the same and the uses thereof as inhibitors of dipeptidyl peptidase IV (DPP-IV), wherein the substitutes in formula (I) have the same meanings as what is mentioned in the descriptions.
Studies of the solid-phase Pauson-Khand reaction: Selective in-situ enone reduction to 3-azabicyclo[3.3.0] octanones
Becker, Daniel P.,Flynn, Daniel L.
, p. 2087 - 2090 (2007/10/02)
The Smit-Caple DSAC Pauson-Khand cyclization of a series of N-protected allyl propargyl amines in the absence of oxygen gave rise to formation of the saturated azabicyclo[3.3.0]octanones in excellent yields. Standard cyclization in air gave mixtures of sa
The Synthesis of Nitrogen Heterocycles via the Intramolecular Khand Reaction: Formation of Tetra- and Hexa-hydrocyclopentapyrrol-5(1H)-ones and Hexahydro-6H-2-pyrindin-6-ones
Brown, Scott W.,Pauson, Peter L.
, p. 1205 - 1209 (2007/10/02)
Azabicyclooctenones and azabicyclononenones have been obtained by cyclisation of hexacarbonyldicobalt complexes of aza-heptenynes and -octenynes respectively.An unusual feature of the cyclisation of N-acyl-4-azahept-1-en-6-ynes is the extens
