Inactivation of horseradish peroxidase by 3,5-dicarbethoxy-2,6-dimethyl-4-ethyl-1,4-dihydropyridine
✍ Scribed by Sugiyama, Katsumi; Woods, Amina; Cotter, Robert J.; Highet, Robert J.; Darbyshire, John F.; Osawa, Yoichi; Gillette, James R.
- Book ID
- 126159661
- Publisher
- American Chemical Society
- Year
- 1994
- Tongue
- English
- Weight
- 761 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0893-228X
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📜 SIMILAR VOLUMES
In the optically active title compound, C 32 H 30 N 2 O 8 , the substituted 1,4-dihydropyridine ring adopts a flattened boat conformation. The crystal structure is stabilized by intermolecular N-HÁ Á ÁO hydrogen bonding. ## Data collection Bruker SMART 1000 CCD diffractometer Absorption correctio
In the molecule of the title compound, C 21 H 28 N 2 O 5 , the substituted 1,4-dihydropyridine (1,4-DHP) ring has a flattened-boat conformation. The carbonyl groups of the ester groups, at positions 3 and 5 in the 1,4-DHP ring, have cis configurations with respect to the double bonds in the 1,4-DHP