17803-12-2Relevant articles and documents
Design, synthesis, and evaluation of cytotoxic activities of arylnaphthalene lignans and aza-analogs
Ourhzif, El-Mahdi,Paris, Arnaud,Abrunhosa-Thomas, Isabelle,Ketatni, El Mostafa,Chalard, Pierre,Khouili, Mostafa,Daniellou, Richard,Troin, Yves,Akssira, Mohamed
, (2021)
A concise and versatile synthetic strategy for the total synthesis of arylnaphthalene lignans and aza-analogs was developed. The main objective was to develop synthetic tactics for the creation of the lactone and lactam unit that would give access to an a
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
-
, (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
A simple method for the synthesis of 4-aryl-9-oxynaphthofuranone lignans
Kobayashi, Kazuhiro,Maeda, Kouji,Uneda, Tomokazu,Morikawa, Osamu,Konishi, Hisatoshi
, p. 443 - 446 (2007/10/03)
The 9-aryl-4-oxynaphthofuran-1(3H)-one system is generally synthesized in two steps from α-aryl-o-toluic acid derivatives. The method involves a tandem conjugate addition-Dieckmann type condensation between α-lithiated α-aryl-o-toluic acid derivatives and
