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Direct and Metal-Catalyzed Photochemical Dimerization of the Phthalide (Z)-Ligustilide Leading to Both [2 + 2] and [4 + 2] Cycloadducts: Application to Total Syntheses of Tokinolides A-C and Riligustilide.
Sheng, Bingbing; Vo, Yen; Lan, Ping; Gardiner, Michael G; Banwell, Martin G; Sun, Pinghua.
Afiliación
  • Sheng B; Institute for Advanced and Applied Chemical Synthesis , Jinan University , Zhuhai , 519070 , China.
  • Vo Y; Research School of Chemistry, Institute of Advanced Studies , The Australian National University , Canberra , ACT 2601 , Australia.
  • Lan P; Institute for Advanced and Applied Chemical Synthesis , Jinan University , Zhuhai , 519070 , China.
  • Gardiner MG; Research School of Chemistry, Institute of Advanced Studies , The Australian National University , Canberra , ACT 2601 , Australia.
  • Banwell MG; Institute for Advanced and Applied Chemical Synthesis , Jinan University , Zhuhai , 519070 , China.
  • Sun P; Research School of Chemistry, Institute of Advanced Studies , The Australian National University , Canberra , ACT 2601 , Australia.
Org Lett ; 21(16): 6295-6299, 2019 08 16.
Article en En | MEDLINE | ID: mdl-31381356
ABSTRACT
Synthetically derived (Z)-ligustilide (1) has been subjected to photochemically-promoted dimerization processes under a range of conditions. By such means, varying distributions of the dimeric natural products tokinolides A-C (4, 3, and 6, respectively) and riligustilide (5) as well certain related (isomeric) compounds have been obtained. The structures of three of them have been confirmed by single-crystal X-ray analysis. The biosynthetic implications of the outcomes of this study are discussed.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Benzofuranos / 4-Butirolactona Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2019 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Benzofuranos / 4-Butirolactona Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2019 Tipo del documento: Article País de afiliación: China