114605-46-8Relevant articles and documents
Symmetry-based approach to oligostilbenoids: Rapid entry to viniferifuran, shoreaphenol, malibatol A, and diptoindonesin G
Jung, Youngeun,Singh, Dileep Kumar,Kim, Ikyon
supporting information, p. 2689 - 2693 (2017/01/09)
The recognition of the local symmetric image within benzofuran-based natural oligostilbenoids guided us to design a modular synthetic approach to these molecules by utilizing a three-step sequence consisting of Sonogashira coupling, iodocyclization, and S
Construction of the biaryl-part of vancomycin aglycon via atropo-diastereoselective Suzuki-Miyaura coupling
Leermann, Timo,Broutin, Pierre-Emmanuel,Leroux, Frederic R.,Colobert, Franoise
experimental part, p. 4095 - 4102 (2012/06/15)
An atropo-diastereoselective synthesis with dr up to 98/2 towards the biaryl subunit of vancomycin based on the use of enantiopure β-hydroxysulfoxide derivatives as novel chiral auxiliary is reported.
Chemical synthesis of funicone analogs
Manzo, Emiliano,Ciavatta, Maria Letizia
experimental part, p. 4107 - 4111 (2012/07/28)
Deoxyfunicone, rapicone and their 5,6-epoxy-derivatives are γ-pyrone compounds with cytostatic and antiproliferative properties. Here we describe a synthesis of these compounds by carbonylative Stille coupling between kojic acid derivatives and functional