名称:
                                The first total synthesis of potent human chymase inhibitor SPF32629B via regioselective bromination and O-acylation strategy
                             
                            
                                摘要:
                                An efficient total synthesis of (+/-)-SPF32629B is described. The key features of the synthesis include regioselective bromination followed by carboxylation at C-3 and protecting-group-free regioselective acylation of hydroxyl group present at C7. Structure was determined by X-ray analysis. (C) 2010 Elsevier Ltd. All rights reserved.
                             
                                                            
                                    DOI:
                                    10.1016/j.tetlet.2010.03.091