- 영문명
- Multicyclization Reaction of 2,3-Dichloro-1,4-Naphthoquinone
- 발행기관
- 대한약학회
- 저자명
- 김순옥(Soon Ok Kim) 박재경(Jae Kyoung Park) 홍사미(Sa Mi Hong)
- 간행물 정보
- 『약학회지』제39권 제3호 (1995년), 118~130쪽, 전체 13쪽
- 주제분류
- 의약학 > 기타의약학
- 파일형태
- 발행일자
- 1995.06.30

국문 초록
영문 초록
Aliphatic and aromatic compounds with two nucleophilic functional groups which were chosen as nucleophiles reacted with 2,3-dichloro-1,4-naphthoquinone as a substrate to give cyclized products by nucleophilic vinyl substitution. And the trends in the synthesis of the heterocyclic compounds were studied and expounded. Besides, the biological activities of the products, especially activity as an agricultural chemical, were examined. Moreover 5-aminomethyl-2-pyrrolidinone was synthesized for the purpose of forming a polynuclear heterocyclic compound containing a similar structure of azasteroid. However only one chlorine of 2,3-dichloro-1,4-naphthoquinone was replaced by an amino group of pyrrolidinone and cyclization did not take place.
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