名称:
                                Enantioselective total synthesis of idesolide via NaHCO3-promoted dimerization
                             
                            
                                摘要:
                                The enantioselective total synthesis of idesolide has been accomplished in 20% overall yield from a known allylic alcohol by a nine-step sequence involving the Sharpless asymmetric epoxidation as the source of chirality and an efficient NaHCO3-promoted dimerization of the monomeric form of idesolide as the key transformation. (C) 2010 Elsevier Ltd. All rights reserved.
                             
                                                            
                                    DOI:
                                    10.1016/j.tet.2010.05.034