158817-23-3Relevant articles and documents
Total synthesis of two γ-butyrolactone containing compounds (Z,11S)-3,4-trans-11-hydroxy-3-methyldodec-cis-6-en-4-olide and (Z)-3,4-trans-11-oxo-3-methyldodec-cis-6-en-4-olide
Nomula, Rajesh,Raju, Galla,Radha Krishna, Palakodety
supporting information, p. 5976 - 5978 (2014/12/12)
The first total synthesis of (Z,11S)-3,4-trans-11-hydroxy-3-methyldodec-cis-6-en-4-olide and (Z)-3,4-trans-11-oxo-3-methyldodec-cis-6-en-4-olide was accomplished using Jacobsen hydrolytic kinetic resolution, Ohira-Bestmann reaction, regioselective alkyne
InCl3-mediated intramolecular Friedel-Crafts-type cyclization and its application to construct the [6-7-5-6] tetracyclic scaffold of liphagal
Jiang, Hao,Tian, Lufeng,Li, Zhentao,Liu, Qi,Li, Chuangchuang,Yao, Xinsheng,Yang, Zhen
, p. 36 - 42 (2012/03/22)
A unified strategy toward the construction of the [5.7.6]tricyclic skeleton of liphagal is reported, featuring InCl3-mediated intramolecular Friedel-Crafts-type cyclization.
Palladium-catalyzed couplings to nucleophilic heteroarenes: The total synthesis of (-)-frondosin B
Hughes, Chambers C.,Trauner, Dirk
, p. 9675 - 9686 (2007/10/03)
The total synthesis of (-)-frondosin B, the enantiomer of naturally-occuring (+)-frondosin B, is described, wherein a palladium-catalyzed cyclization is used to establish the tetracyclic ring system of the natural product. Graphical Abstract.