(2SR,8aSR)-1,2,3,4,6,7,8,8a-Octahydro-6-oxonaphthalene-2-acetic acid: hydrogen bonding in an unsaturated bicyclic keto acid

Autor: Janish Desai, Hugh W. Thompson, Roger A. Lalancette, Muhammad H. Malak
Rok vydání: 2007
Předmět:
Zdroj: Acta Crystallographica Section E Structure Reports Online. 63:o3606-o3606
ISSN: 1600-5368
DOI: 10.1107/s1600536807035003
Popis: The title racemate, C12H16O3, aggregates in the solid state as translational acid-to-ketone hydrogen-bonded catemers. The stereochemistry of the side chain relative to the ring junction arises spontaneously during the synthesis. The four hydrogen-bonding chains passing through the unit cell are of alternating handedness, and are aligned along the [101] direction. Starting at the origin, the order of the directional alignment of these four chains with respect to the a axis is ++−−. One inter­molecular C—H⋯O=C close contact exists to the carboxyl O atom.
Databáze: OpenAIRE