## Abstract Chemical ionization induced fragmentations (with 2‐methylpropane as reagent gas) of 4‐methyl‐ and 4,5‐dimethyl‐2‐phenyl‐1,3,2‐dioxaborolane and 4‐methyl‐2‐phenyl‐1,3,2‐dioxaborinane gave in each case two fragments, a hydrocarbon ion and metaboric acid. Propeae and thence metaboric acid
Formation of 3-phenyl quinoline from 2-phenyl-3-(2′-chlorophenyl)-2-propenenitrile under chemical ionization conditions
✍ Scribed by K. P. Madhusudanan; V. Srinivas Murthy; D. Fraisse
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 196 KB
- Volume
- 21
- Category
- Article
- ISSN
- 1076-5174
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## Abstract magnified image Benzyl cyanide reacts with triethylorthoformate and piperidine in DMF solution to yield the title compound **2**. This reacted with aromatic amines to yield either aminoacrylonitriles or quinoline depending on reaction conditions and substitution pattern on the aromatic