ANODIC-OXIDATION AS A SYNTHETIC EXPEDIENT TO NAPHTHOQUINONE AND ANTHRAQUINONE KETALS
Publication in refereed journal


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其它資訊
摘要Some naphthoquinone and anthraquinone ketals have been prepared by anodic oxidation. Regioselective hydrolysis of the above diketals into monoketals is also described. Diels-Alder reaction of (E)-1-methoxybuta-1,3-diene with the monoketal of 1,4-dihydro-4,4-dimethoxy-5-benzyloxynaphthalene proceeded in a regioselective manner.
著者YANG Z, CUI YX, WONG HNC, WANG RJ, MAK TCW, CHANG HM, LEE CM
期刊名稱Tetrahedron
出版年份1992
月份4
日期17
卷號48
期次16
出版社PERGAMON-ELSEVIER SCIENCE LTD
頁次3293 - 3302
國際標準期刊號0040-4020
語言英式英語
關鍵詞ANTHRAQUINONE KETALS; DIELS-ALDER REACTION; NAPHTHOQUINONE KETALS; REGIOSELECTIVE HYDROLYSIS
Web of Science 學科類別Chemistry; Chemistry, Organic; CHEMISTRY, ORGANIC

上次更新時間 2021-17-01 於 00:34