【摘 要】
:
Previously we have achieved an one-pot tandem Wittig-cyanosilylation sequence,in which the by-product Ph3PO from the Wittig step were internally recycled as indispensable co-catalysts for the followin
【机 构】
:
Shanghai Key Laboratory of Green Chemistry and Chemical Processes,School of Chemistry and Molecular
【出 处】
:
中国化学会全国第十二届有机合成化学学术研讨会
论文部分内容阅读
Previously we have achieved an one-pot tandem Wittig-cyanosilylation sequence,in which the by-product Ph3PO from the Wittig step were internally recycled as indispensable co-catalysts for the following asymmetric cyanosilylation step.1 As an effort to extend the utility of such an highly atom-economical tandem reaction,we have recently focused on an one-pot protocol for the highly enantioselective synthesis of versatile chiral conjugated dienes and enynes,the key step of which is an unprecedented asymmetric cyanosilylation of α,β,γ,δ-unsaturated enones.
其他文献
Low molecular-mass organic gelators(LMOGs)have generated considerable interest during the past decade for the design of smart materials.In recent years,self-assembly of TTF derivatives through intermo
喹啉类衍生物在药物、农药、染料和化学助剂方面一直占有十分重要的地位,因此,许多有机化学工作者也一直热衷于研究喹啉衍生物的合成方法。但是,传统的化学合成法大多需要使用无机酸、碱性物质,存在对反应设备要求高,催化剂不易与反应体系分离且不可重复利用,会产生大量废水,环境不友好等问题,因此,新型绿色化学催化剂的研究、开发、利用、催化剂作用机理的研究,对于喹啉类衍生物的合成来说就显得尤为重要。
冠醚与碱金属、碱土金属有良好的配位作用,在过去的数十年中基于大环冠醚络合分离碱金属、碱土金属离子(特别是锂离子)的技术被广泛研究。如冠醚液液萃取法、基于冠醚主体的离子交换树脂法等。然而,传统的冠醚尽管对金属离子的络合能力较强,但存在反萃率低、电荷不呈中性等缺陷。因此,对于相应的分离技术仍然存在挑战。在此,我们引入了硼原子辅助冠醚关环,由于硼氧关环可被亲硼性氟离子开环而发挥选择性的离子络合开关作用,
本研究以抗肿瘤药喜树碱为模板,DT1 为功能单体、DT2 为第一交联剂、马来松香丙烯酸乙二醇酯为第二交联剂,利用马来松香丙烯酸乙二醇酯交联剂较好的手性空间立体选择性和机械强度,通过悬浮聚合法合成松香基手性高分子印迹聚合物,其粒径主要集中在50um.将松香基手性高分子印迹聚合物作为固定相,获得松香基手性高分子印迹色谱柱,用高效液相色谱法评价其识别位点和喜树碱之间的匹配程度,研究其印迹效果和分离性能.
A series of β-keto acids can be α-functionalized by a series of glycols to produce some C-glycosides shown asfollows[1]:Comparatively,a series ofβ-keto acids also can beα-functionalized by a series of
吡啶并[1,2-a]咪唑类化合物在医药领域表现出了良好的生物和药物活性[1],而此类化合物的药物活性则取决去其不同位置所联有的官能团。在各种各样的吡啶并[1,2-a]咪唑类化合物当中,其亚硝基化的化合物由于在生物代谢过程中的重要作用受到了广泛的关注[2],并且此类化合物是许多化学反应,如aldol 反应、Diels-Alder 反应以及环加成反应等的中间体。
β-Sulfonium carbanions,as a member of organosulfur family,are ephemeral intermediates and difficult to be applied in organic synthesis.We developed a new strategy to relatively stable β-sulfonium carb
The selective introduction of a fluoroalkyl group into bioactive molecules has been established as a powerful strategy in drug design to modulate pharmacological properties,which stimulates the develo
Aurones(3)have exhibited a wide range of biological activities and have been used as antifungal agents,tyrosinase inhibitors,antioxidants,and others.Due to the importance of aurones,recently we focuse
Thiophenes are unique sulfur-containing heterocycles and attracted particular attention due to their special place as building blocks in natural products,pharmaceutical agents and materials.Especially