Detail of "2887-98-1"
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Reference
- Photochemical reactions of high polymers
- Photochemical reactions of high polymers. XVI. Quenching effect of oximes on the photolysis of copolymers of styrene and phenyl vinyl ketone. Tsunooka, Masahiro; Nishino, Todomu; Tanaka, Makoto (Fac. Eng., Univ. Osaka Prefect., Sakai, Japan). Chem. Lett., (9), 1107-8 (English) 1977. CODEN: CMLTAG. DOCUMENT TYPE: Journal CA Section: 35 (Synthetic High Polymers) Benzylidene acetone oxime [2887-98-1] and 2-acetonaphthone oxime [51674-06-7] were as effective as naphthalene [91-20-3] as quenchers in the photolysis of phenyl vinyl ketone-styrene copolymer [27340-61-0] in benzene soln. or in the solid phase.
- Organoselenium-induced isoxazoline formation from a,b-unsaturated ketone hydroxime
- Organoselenium-induced isoxazoline formation from a,b-unsaturated ketone hydroxime. Terao, Keiji (Wacker Chem. East Asia Ltd., Tokyo 169, Japan). Chem. Express, 7(2), 161-4 (English) 1992. CODEN: CHEXEU. ISSN: 0911-9566. 2887-98-1 and 2158-24-9 are cas registry numbers of chemicals which are used as reagents here. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Addn. of PhSeCl to PhCH:CHCMe:NOH in MeOH did not give the expected double bond addn. product, but rather isoxazoline I (R = Ph, R1 = H) in 30-54% yields. Similarly, cyclocondensation of PhSeCl with Me2C:CHCMe:NOH gave I (R = R1 = Me) in 38% yield. .


