化学药物(复杂有机物)系统命名的步骤与方法

理解并掌握药物化学名是药学专业学生和药师在药物化学学习和药学服务工作中经常遇到的难题。本文在广泛查阅文献资料的基础上系统、详细地总结化学药物系统命名的步骤和方法,同时对《有机化合物命名原则(2017)》与《有机化学命名原则(1980)》进行对比,并结合2个代表药进行解释说明。该步骤和方法具有系统、详细的特点,对药学专业学生和药师理解并掌握药物化学名具有较大的帮助作用。     

构建“三三三”混合式课堂教学新模式——以“原子结构”类比模型的建构为例(Ⅰ)

基于在线开放课程和移动互联技术，探讨了医药类院校"无机化学"课堂教学的重构。实践中依托"一平台、一区域、六模块"，运用移动互联思维重构了三阶段、三环节、三分类的"三三三"教学新模式。进一步以"原子结构"为例介绍了课堂重构的教学设计。教学改革从学生问卷调查、考试成绩、能力培养以及学习心理等不同角度均得到非常积极的反馈，期望这一理念和实践能为新时期高校课堂教学和人才培养提供参考。     

Rasch模型在“化学键”概念教学评价中的应用研究

运用Rasch模型探查高二学生对"化学键"概念的认知情况，运用Conquest软件和Winsteps软件对测试结果进行分析。结果表明：基于Rasch模型编制的测试卷能客观有效地检测学生对"化学键"概念的理解，为一线教师的有效教学提供学情基础。     

化学社会课程资源开发及教学范例——水的净化与水资源保护

课程资源逐步走向开放化、共享化和社会化，社会已成为实施教育教学活动的重要场所。以"水的净化与水资源保护"主题内容为教学范例，提出了化学社会课程资源开发的思路和教学实施流程：在"前置学习"中通过社会课程资源的亲身实践，把化学的课堂延伸到社会领域；在"展示分享"中将获取的有效资源与课堂学习关联，实现知识与生活的有效链接；在"整理评价"中完成知识建构和巩固过程，让学生感受真实、有用的化学。     

以“绿色化学”为例浅谈通识教育公共选修课的课程建设与教学改革

详细阐述了综合性大学本科通识教育公共选修课"绿色化学"的课程建设、教学实践与改革探索，通过对教学侧重点的细致化、课程难易程度的普适化、教学手段的多样化和考评机制的合理化改革，大大激发了各专业学生的学习兴趣，显著提高了公选课的教学效果，既明确了"绿色化学"作为各专业通识教育课程的总体建设目标与实施方案，也为其他化学类通识教育课程的建设提供了可借鉴的教学经验和改革思路。     

以药物分子结构修饰为主题设计习题发展学生核心素养

以青蒿素、水杨酸、阿司匹林等药物分子结构修饰的发展史为素材设计了3组习题，分析了习题对促进学生"宏观辨识与微观探析""创新意识""模型认知""科学态度与社会责任"等化学核心素养发展的价值，论述了与素养达成目标相对应的关键能力的具体表现。     

选准代表物质 开辟探究路径 培育核心素养——“卤代烃”的创新教学

在卤代烃的课堂教学实践中，选定1-溴丙烷为代表物，依据化学键理论并结合模型认知、实验探究等方式创新设计课堂教学，既规避和弥补按某些教材教学带来的尴尬与不足，又能突破教学难点（卤代烃消去反应原理），更能培育"宏观辨识与微观探析""证据推理与模型认知""科学探究与创新意识""科学态度与社会责任"等学科核心素养。     

医用有机化学波谱分析绪论部分的教学研究

概述了问题导向式的研究型教学设计在医科院校"医用有机化学"课程中有机波谱分析章节的应用情况。该部分内容具有学生"难学" "难考" ，教师"难教"的教学特点。基于此，通过层层设问、循序解答的授课方式，结合丰富的应用示例，进行有机波谱分析核心概念（绪论）的理论教学。结果表明，该教学方法可有效提高学生学习兴趣，降低学习难度，使学生在有限的学时内掌握有机波谱分析的基础理论与核心概念，为后续识谱、解谱能力的培养夯实基础。     

以学生为中心的递进式“精细化工”实验教学

针对学生实验课积极性不高、实验教学效果不理想的问题，对一门选修课"精细化工"的实验进行了重新思考和设计，让学生参与从实验具体内容制定、操作到结果讨论的整个过程，并首次以"递进式"实验的方式由学生参与第2次实验（基于前一个实验的改进和完善），使学生了解理论知识转化为可行实验方案的具体做法，切身体会在实验原理相同的情况下，实验方案的细微调整对实验结果的巨大影响。结果表明，这种"以学生为中心"的改进能让学生注重实验细节，同时关注实验失败的原因，并在第2次实验中及时修正。这为学生实验综合素质的培养提供了一种教学思路。     

基于化学学科核心素养的“铁盐和亚铁盐”教学设计

以"铁盐和亚铁盐"教学为例，从"暖宝宝"这一情境出发，创设了"暖宝宝使用前后发生了什么变化" "使用后暖宝宝中铁元素可能存在的价态是什么、如何验证" "如何回收利用暖宝宝中的铁元素"3个问题情境，通过引导学生积极开展探究学习和问题解决，培养学生"宏观辨识与微观探析" "证据推理与模型认知" "科学探究与创新意识""科学态度与社会责任"等化学学科核心素养。     

二氧化碳和丙烯直接合成甲基丙烯酸的NiPMo/TiO2催化剂的研究

用溶胶-凝胶法以磷钼酸(MPA)的镍盐溶液水解钛酸四丁酯制备了NiPMo/TiO2催化剂.使用ICP、 XRD、 TG-DTA、 IR、 TPD-MS和微反应技术研究了催化剂的化学组成、热稳定性、化学吸附性质和催化反应性能.杂多钼酸盐与TiO2通过O2-在TiO2表面发生了键合.在623 K下,杂多阴离子仍保持原有的Keggin结构.CO2在Lewis酸位Ni(Ⅱ)和Lewis碱位Ni-O-Mo的桥氧协同作用下生成CO2卧式吸附态Ni(Ⅱ)←O-(CO)←(O--Ni).丙烯有多种吸附态在催化剂上吸附.在563 K、 1 MPa和空速1500 h-1的反应条件下,丙烯的摩尔转化率为3.2%,产物MAA选择性为95%.     

Toward new camptothecins. Part 6: Synthesis of crucial ketones and their use in Friedländer reaction

In the context of the preparation of camptothecin and luotonin A analogs, the synthesis of some key keto-precursors and their use in Friedländer condensation are described. This paper also focuses on the stability of these keto intermediates and emphasizes the major differences between indolizinones and pyrroloquinazolinones series. Noteworthy is also the report of some original structures isolated as by-products of some experiments.     

α-Amino acid derived enaminones and their application in the synthesis of N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates and other heterocycles

A new and simple synthesis of novel N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates, which exist in equilibrium with their 4-oxo tautomers, has been developed in two steps starting from N-protected α-amino acids. The key intermediates are enaminones, which can also be isolated, characterized, and used for the construction of other functionalized heterocycles, before they spontaneously decompose to pyrrole products. 4-Hydroxypyrroles are prone to partial aerial oxidation but can be efficiently alkylated or reduced to stable polysubstituted pyrrolidine derivatives.     

Specific intramolecular aromatic CH insertion of diazosulfonamides

The chemoselectivity in the intramolecular CH insertion of various diazosulfonamides has been experimentally studied. The results reveal that the aliphatic 1,4-, 1,5-, or 1,6-C(sp³)?H insertions of diazosulfonamides are not accessible, while the aromatic 1,5-C(sp²)?H insertion can be realized specifically by adjusting the diazo-adjacent group. In addition, the general chemoselectivities in the intramolecular CH insertions of diazosulfonyl compounds are summarized. Generally, diazosulfones undergo both aromatic 1,5-C(sp²)?H and aliphatic 1,5- and 1,6-C(sp³)?H insertions, while diazosulfonates undergo aliphatic 1,5- and 1,6-C(sp³)?H insertions. However, diazosulfonamides only undergo aromatic 1,5-C(sp²)?H insertion.     

CoFe2O4自形成磁性液体场致结构化对磁化的影响

The Langevin paramagnetic theory can’t describe the relation between magnetization of ferrofluids and applied magnetic field. The structuralization of ferrofluids, which is considered the main influence factor of the magnetization, is regarded. The part of magnetization works is deposited when the structure is forming. This action influences the magnetization of ferrofluids directly or indirectly. On the base of the “compressing” model, the Langevin function that usually describes the magnetization of ferrofluid is modified, and a well-fitted curve is obtained. An equation of the relation between the equivalent volume fraction after being “compressed” and the intensity of magnetic field is discovered, which approximately describes the process of magnetization. The relation between the approximate initial susceptibility and the volume fraction can be obtained from modified formula.     

KMnO4-mediated oxidative CN bond cleavage of tertiary amines: Synthesis of amides and sulfonamides

KMnO₄-mediated oxidative CN bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride and sulfonyl chloride) to form amides and sulfonamides. The reaction could take place at mild condition, tolerating a wide range of function groups and affording products in moderate to excellent yields.     

Highly regioselective Buchwald–Hartwig amination at C-2 of 2,4-dichloropyridine enabling a novel approach to 2,4-bisanilinopyridine (BAPyd) libraries

The highly regioselective Buchwald–Hartwig amination at C-2 of the cheap and readily accessible reagent, 2,4-dichloropyridine with a range of anilines and heterocyclic amines is described. This new methodology is robust and provides a facile access to 4-chloro-N-phenylpyridin-2-amines on 0.25 mol scale. These intermediates undergo a further Buchwald–Hartwig amination at higher temperature to enable rapid exploration of the chemical space at C-4 and to provide a library of 2,4-bisaminopyridines.     

Chemistry of heterocyclic compounds at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, over 50 years (Review)

The review contains a concise historical account and information on the most significant researches undertaken by the staff at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences on the Chemistry of Heterocyclic Compounds. Dedicated to Academician of the Russian Academy of Sciences B. A. Trofimov on his 70th jubilee. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1443–1502, October, 2008.     

N-Heterocyclic carbene-palladacyclic complexes: synthesis,characterization and their applications in the C-N coupling and α-arylation of ketones using aryl chlorides

N-Heterocyclic carbene-palladacyclic complexes 3 were successfully achieved in a one-pot procedure under mild conditions. The structure of 3a was unambiguously confirmed by X-ray single crystal diffraction and it was an active catalyst in the Buchwald-Hartwig amination and α-arylation of ketones even at very low catalyst loadings (0.01?mol%).     

Iodine-mediated oxidative Pictet-Spengler reaction using terminal alkyne as the 2-oxoaldehyde surrogate for the synthesis of 1-aroyl-β-carbolines and fused-nitrogen heterocycles

An efficient iodine-mediated oxidative Pictet-Spengler reaction in dimethyl sulphoxide (DMSO) using terminal alkynes as the 2-oxoaldehyde surrogate for the synthesis of aryl (9H-pyrido[3,4-b]indol-1-yl)methanones is described. The scope of the protocol includes the total synthesis of Fascaplysin, Eudistomins Y₁ and Y₂. The methodology is extended for preparing pyrrolo[1,2-a]-quinoxaline and indolo[1,5-a]quinoxaline derivatives. The utility of 1-aroyl-β-carbolines was demonstrated by performing palladium-catalyzed β-carboline directed ortho-C(sp2)-H functionalization of the phenyl ring with thiomethyl (SMe) group using DMSO as source and for accessing 4-aryl-canthin-6-ones.