3672-60-4Relevant academic research and scientific papers
A novel bicyclic system, 1,6-diaza-3,8-dioxabicycloundecane
Kostyanovsky, R. G.,El'natanov, Yu. I.,Krutius, O. N.,Chervin, I. I.,Zaddach, H.,Koehler, K. F.
, p. 321 - 322 (1994)
Condensation of monoethanolamine with formaldehyde affords 1,6-diaza-3,8-dioxabicycloundecane and N,N'-methylene-bis(oxazolidine) in a ratio of 1:8. - Key words: monoethanolamine, formaldehyde, condensation; 1,6-diaza-3,8-dioxabicycloundecane, N,N'-methylene-bis(oxazolidine), NMR spectra.
First synthetic method for the preparation of 6-unsubstituted-2,3-dihydro-1,3-oxazin-4-ones
Bertolini, Giorgio,Aquino, Mario,Ferrario, Francesco,Pavich, Gianfranco,Zaliani, Andrea,Sala, Alberto
, p. 3358 - 3361 (2007/10/03)
The first synthetic pathway to synthesize 6-unsubstituted-2,3-dihydro-1,3-oxazin-4-ones is described. The α-formylation of the starting amide and the cyclization of the α-formylamide with a desired aldehyde under acidic conditions gave compounds 5a-h (R = nPr, iPr, cPr, cHex, Ph, CH2Ph, nHex, and R1 = H, Me). This strategy was used with little modification for the preparation of new monocyclic organic nitrates such as 2a-c (2a (R = Ph, R1 = H, and R2 = H), 2b (R = Ph, R1 = H, and R2 = Me), and 2c ( R = H, R1 = Ph, and R2 = H).
Heterocyclic Deformations from Molecular Enlargement
Lambert, Joseph B.,Wharry, Stephen M.
, p. 3890 - 3893 (2007/10/02)
The ease of distortion of saturated nitrogen heterocycles has been examined by progressively increasing the bulk of the substituent at nitrogen.The heterocycles included the pharmacophoric piperidine and morpholine six-membered rings, as well as the five-membered oxazolidine ring.Response to increased bulk of substitution was intended to be a crude model for distortions within the drug-receptor complex.Substitution at nitrogen included methyl, (1-adamantyl)methyl, and 6-substituted β-cyclodextrin within a tetrahedral series, and acetyl and (1-adamantyl)carbonyl within a trigonal series.With methyl and acetyl serving as standards for the undistorted rings, we have found that the NCH2CH2X dihedral angle within all three heterocycles is decreased anly by about 1 deg on introduction of adamantyl groups.In agreement with this flattening distortion, the barrier to ring reversal of the piperidine is decreased by 1.4 kcal/mol on replacement of N-methyl by N-adamantylmethyl.The β-cyclodextrin ring imposes a much more severe distortion, as this same dihedral angle in the piperidine and morpholine rings decreases 5-6 deg.The barrier to rotation about the amide bond decreases 5-6 kcal/mol in all three heterocycles on going from acetyl to adamantylcarbonyl.These studies show that the response of these heterocycles to incresed steric bulk of N substitution is a flatter and hence more flexible ring.
