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서지반출
Photochemical Formation of 3-Methoxycyclohex-2-en-1-ones from 1,3-Cyclohexanedione and 2-Allyl-3-hydroxycyclohex-2-en-1-one in Methanol in the Presence of Quinones
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  • Photochemical Formation of 3-Methoxycyclohex-2-en-1-ones from 1,3-Cyclohexanedione and 2-Allyl-3-hydroxycyclohex-2-en-1-one in Methanol in the Presence of Quinones
  • Photochemical Formation of 3-Methoxycyclohex-2-en-1-ones from 1,3-Cyclohexanedione and 2-Allyl-3-hydroxycyclohex-2-en-1-one in Methanol in the Presence of Quinones
저자명
Kim. Sung-Sik,Chang. Ji-Ae,Kim. Ae-Rhan,Mah. Yoon-Jung,Kim. Hyun-Jin,Kang. Chan
간행물명
Journal of photoscience: an international journal officail organ of the Korean Society of Photoscience
권/호정보
2000년|7권 3호|pp.111-114 (4 pages)
발행정보
한국광과학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
서지반출

기타언어초록

Irradiation of 1,3-cyclohexanedione and p-benzoquinone in methanol gave 3-methoxycyclohex-2-en-1-one. Allyl derivative of the 1,3-diketone was prepared as enol from and irradiated in methanol in the presence of p-benzoquinone to give the same type of photoproduct, i.e., 2-allyl-3-methoxycyclohex-2-en-1-one. Allyldibenzoylmethane was synthesized and irradiated with p-benzoauinone in methanol but no remarkable amount of photoproduct was obtained.