22743-05-1Relevant articles and documents
Michael Initiated Ring Closure reactions in natural product synthesis: A concise entry to the podophyllins
Harrowven, David C.
, p. 9039 - 9048 (1993)
A rapid entry towards the Podophyllum lignans is described exemplified by a concise regioselective total synthesis of taiwanin E 5 and chinensinaphthol 6. The approach features a Michael Initiated Ring Closure (MIRC type II) sequence to access the key lig
An Optimized and General Synthetic Strategy To Prepare Arylnaphthalene Lactone Natural Products from Cyanophthalides
Kim, Taejung,Jeong, Kyu Hyuk,Kang, Ki Sung,Nakata, Masaya,Ham, Jungyeob
, p. 1704 - 1712 (2017/04/13)
A simple method for the preparation of arylnaphthalene lactone natural products was developed and used to synthesize diphyllin (10), justicidin A (12), cilinaphthalide B (13), taiwanin E (15), chinensinaphthol (16), taiwanin E methyl ether (17), chinensin
METHOD FOR PREPARATION OF JUSTICIDIN A DERIVATIVES OF ARYLNAPHTHALENE LIGNAN STRUCTURE
-
Paragraph 114; 374; 375; 376; 377, (2014/08/19)
The present disclosure relates to a novel method for preparing an arylnaphthalene lignan compound. In synthesis of arylnaphthalene lignan compounds and derivatives according to the present disclosure, a naphthalene backbone may be constructed first and an