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Oxepane, conformational analysis

The conformational analysis of oxepane conducted within the MM2 and MM3 force fields shows a preference for the twist-chair conformation, which can be explained based on nonbonding interactions between hydrogen atoms <1994JST247>. [Pg.47]

The oxepane and oxepanone derivatives 51 and 52 respectively, were made by allylindation of, or allylmagnesium bromide addition to, acyclic tetrakis(tetrahydrofuranyl) dialdehydes. The solid state conformation of 52 was determined by X-ray diffraction analysis <00JOC4303>. [Pg.351]

See other pages where Oxepane, conformational analysis is mentioned: [Pg.126]    [Pg.168]    [Pg.183]    [Pg.48]    [Pg.234]    [Pg.169]    [Pg.32]   
See also in sourсe #XX -- [ Pg.234 ]



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