机译：二肽衍生的膦催化的具有马来酰亚胺的不对称[3 + 2]环烯基芳烃环化反应：轻松创建包含两个叔立体中心的功能化双环环戊烯
Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 MeiLong Road, Shanghai 200237, P. R. China;
Department of Chemistry & Medicinal Chemistry Program, Life Sciences Institute, National University of Singapore, 3 Science Drive 3, Republic of Singapore 117543;
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, P. R. China;
Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 MeiLong Road, Shanghai 200237, P. R. China,State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, P. R. China;
Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 MeiLong Road, Shanghai 200237, P. R. China,Department of Chemistry & Medicinal Chemistry Program, Life Sciences Institute, National University of Singapore, 3 Science Drive 3, Republic of Singapore 117543;
机译：对映异构体[3 + 2]环烯丙二酸酯到二肽衍生的膦所催化的丙烯酸酯的环加成反应：轻松创建包含季立体中心的功能化环戊烯
机译：亚吲哚甙盐催化（3 + 2）含有雄蛋白的环节：两种大亨季矫肌的对映选择性形成
机译：对映选择性合成高度官能化的含三氟甲基的环戊烯：多功能硫脲-膦催化的森田-贝利斯-希尔曼碳酸盐与三氟亚乙基丙二酸酯的不对称环化[3 + 2]
机译：驯服官能团：空气稳定的原发性磷酸和p-tereogenic三膦（摘要）
机译：第一部分：利塞膦酸盐双环类似物的不对称合成，作为双膦酸盐类抗骨质疏松药和潜在更有效的抗骨质疏松药作用机理的分子探针。第二部分使用Bestmann内酯从常见手性助剂轻松制备和官能化手性稳定化的叶基及其在Wittig反应中的用途。第三部分不对称有机催化：1.醛的α-羟基化研究； 2.合成新的基于樟脑的α-氨基四唑有机催化剂。
机译：手性多功能硫脲-膦催化马来酰亚胺的Morita–Baylis–Hillman碳酸盐的不对称3 + 2成环
机译：手性多官能硫脲 - 膦催化morita＆＃8211; Baylis＆＃8211; Hillman碳酸酯与马来酰亚胺的不对称[3 + 2]环化
