Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Topological and Supramolecular Stereochemistry

Topologically, the triangle, circle, and square are all just closed loops (as long as we do not consider the corners of the triangle and square to be vertices). [Pg.324]

Interconversion of the enantiomers of 2-butanol can be accomplished by flexing and bending without crossing any bonds, and so the two enantiomers are topologically equivalent. [Pg.324]


See other pages where Topological and Supramolecular Stereochemistry is mentioned: [Pg.248]    [Pg.324]    [Pg.325]    [Pg.327]    [Pg.327]    [Pg.329]    [Pg.248]    [Pg.324]    [Pg.325]    [Pg.327]    [Pg.327]    [Pg.329]    [Pg.147]    [Pg.16]    [Pg.40]    [Pg.292]    [Pg.292]    [Pg.324]   


SEARCH



Achievements in Topological and Supramolecular Stereochemistry

And stereochemistry

Supramolecular stereochemistry

© 2024 chempedia.info