KOTAKE et al., 1953 - Google Patents
The Resolution of FlavanoneKOTAKE et al., 1953
View PDF- Document ID
- 2519234184076512574
- Author
- KOTAKE M
- NAKAMINAMI G
- Publication year
- Publication venue
- Proceedings of the Japan Academy
External Links
Snippet
Experimental 5-methyl-5-(a-methyl-$-phenyl-ethyl)-semioxamazide.-A mixture of 6 g. of 1- phenyl-2-methylaminopropane (bp 80.5-81 J10mm.) and 6 g. of ethyl oxalate was left in a rubber stoppered container at room temperature for 10 days. After removing the unreacted …
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/82—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups
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