SPOC教学模式在学科教学(化学)教育硕士培养中的应用——以教育技术在中学化学教学中的应用为例

以师范院校面向学科教学(化学)专业教育硕士开设的"教育技术在中学化学教学中的应用"课程为例,研究了SPOC课程教学资源建设的内容、方法,分析了采用翻转课堂的SPOC教学流程的教学设计策略,比较了应用SPOC教学模式前后的学生学习效果。     

翻转课堂在医学院校卫生化学实验教学中的应用

将翻转课堂教学模式引入到预防医学专业卫生化学实验课中,以“高效液相色谱法测定饮料中的山梨酸与苯甲酸”为例分析翻转课堂设计过程,包括任务单设计、教学视频制作、课堂组织、课后评价等诸多环节。实践表明,翻转课堂的应用,激发了非化学专业学生对卫生化学实验的学习兴趣,调动了学习主动性和积极性,使学生由被动接受者变为主动探究者,而教师则由知识传授者转变为学习促进者和指导者,有利于培养学生自主学习能力和创新合作精神。     

后MOOC时期高职分析化学混合式教学模式构建

为了全面提高后MOOC时期的高职院校分析化学课程教学质量，提出了基于SPOC的分析化学课程混合式教学模式。首先分析了高职学生的特点和分析化学课程教学中的主要问题；然后根据基于SPOC的混合式教学模式构建流程，依次阐述了课程分析、整体设计、资源开发、教学过程和评价考核设计的原则与思路；最后探讨了基于翻转课堂的分析化学课程混合式教学环境与实施过程。     

基于多维任务驱动下的物理化学实验课程探索*

设计不同维度的课程任务学习单,并将自主探究、协作交流等学习模式引入物理化学实验的实践教学,深入探讨了物理化学实验课程实施翻转课堂的教学模式的研究。整个教学环节包括:课前资源导学、课内知识拓展、课后成效评价。实践表明,翻转课堂有利于提高学生的知识内化能力、分析解决问题能力、合作交流能力以及自学能力,尤其是文献调研的能力有显著提升,该模式取得了较好的教学效果。     

翻转课堂模式在旋光度测定实验教学中的应用

以糖类物质旋光度的测定为例,探索了翻转教学在医学院校基础有机化学实验教学中的应用。包括设计任务书、制作教学视频及文档、查找相关文献、课堂活动、教学总结及反思等多个环节。实践表明,翻转课堂在实验教学中的应用,改善了课前预习流于形式的状况,培养了学生主动学习的能力,激发了医学专业学生对基础有机化学实验的学习兴趣。     

线上线下混合式教学结合翻转课堂进行酯缩合反应的教学*

采用“线上线下混合式教学”开展有机化学课程的教学工作,利用APP “学习通”将在线课堂教学和线下讲授相结合。以知识点酯缩合反应的教学为例,介绍了该教学模式的实施过程和教学效果。实践结果表明,线上线下混合式教学与翻转课堂相结合的教学模式,能够拓展化学专业学生知识面,提升学生的自主学习能力和学习的积极性,取得了较好的教学效果。     

翻转课堂教学模式在普通化学教学中的应用与评价

首次探讨了在普通化学民族班教学中应用"翻转课堂"的教学模式,并就教学效果进行了评估。翻转课堂教学模式充分调动了民族班学生的学习积极性和主动性,同时提高了教师的教学水平,取得了较好的教学效果。为在对母语为非汉语的学生开设的普通化学课程教学中逐步采用"翻转课堂"教学模式替代传统教学模式提供了成功的经验。     

信息化网络环境下高职应用型课程翻转课堂的教学设计与实施——以“中药制剂检验技术”为例

以"中药制剂检验技术"课程为例,在课前、课内、课后3个阶段,从理论和实践的角度探讨了如何利用N-CLASS网络平台构建和实施高职药品检验类课程的翻转课堂。结果表明,在药品检测类课程中,利用信息技术构建的翻转课堂不仅能够激发学生学习的主动性和学习兴趣,同时也培养了独立学习和协作学习的能力,明显提升了教学效果。     

大学无机化学“原电池”翻转课堂教学研究

通过翻转课堂与传统课堂在学习目标与教学流程上的对比,详细阐述了"原电池"翻转课堂的教学设计特点与实践研究过程,即课前利用微视频和学习单自主学习形成基本概念,课堂上通过解决问题实现重要概念内化,课后通过开放性问题体验原电池的价值。实践结果显示,"原电池"翻转课堂教学设计与实践能够更好地促进学生的发展,并在一定程度上优于传统课堂教学。     

基于教育游戏的翻转课堂教学设计——以“原电池的设计”为例

在国内外翻转课堂相关文献对比和教育游戏特点分析基础上,尝试进行了基于教育游戏的高中化学“原电池的设计”的翻转课堂教学设计,利用教学游戏,充分调动学生的学习兴趣,提高翻转课堂课前学习效率。     

A carbanion induced synthesis of highly congested pyrazole and imidazole containing heterocycles

An efficient approach to the synthesis of highly congested di, penta and hexacyclic pyrazoles as well as imidazole fragment containing novel heterocyclic molecule has been developed through a carbanion induced transformation of suitably functionalized 2H-pyran-2-ones, benzo[h]chromene and thiochromeno[4,3-b]pyrans. Due to the presence of fluorescence, we report their prime application metal sensor as off/on switching in ferric ions.     

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.     

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%).     

Selective synthesis of 4,5-dihydroimidazo- and imidazo[1,5-a]quinoxalines via modified Pictet–Spengler reaction

An efficient tandem approach for the selective synthesis of 4,5-dihydroimidazo[1,5-a]quinoxalines 6a–g and imidazo[1,5-a]quinoxalines 7a–h by the reaction of 2-imidazolyl anilines 4a–c with aryl aldehydes 5a–k under mild reaction conditions is described. Introduction of electron releasing alkyl groups in substrates 4a–b was found to be instrumental for the success of the reaction.     

Understanding the Diels-Alder reactivity of 1,2-azaborine analogues

The Diels-Alder reactivity of 1,2-heteroborines (H₄C₄B(H)X, X?=?NH, PH, AsH; O, S, Se) has been computationally explored by means of Density Functional Theory (DFT) calculations. The influence of the HB?=?X fragment on the reactivity of the system has been quantitatively analyzed in detail by means of the so-called Activation Strain Model (ASM) of reactivity. It is found that the interaction between these species and the dienophile is significantly stronger than that computed for their all-carbon isoelectronic counterpart, benzene. In addition, the strain energy plays a key role in the observed reactivity trends. The role of the aromaticity strength of these heteroarenes on the reactivity is also assessed.     

Synthesis of N-substituted carbazolones from α-iodo enaminones via Pd(0)-catalyzed intramolecular coupling under microwave irradiation

A variety of N-aryl and N-alkyl carbazolones were conveniently achieved in good to high yields via Pd₂(dba)₃-mediated intramolecular coupling of N-substituted α-iodo enaminones under microwave irradiation. The Pd(0)-catalyzed cyclization was found to proceed favorably with the more electron-deficient phenyl ring during the reactions involving unsymmetrical N,N-diaryl α-iodo enaminones. This unique property enables the construction of carbazolone skeleton containing nitro substituted benzenoid ring.     

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.     

Facile synthesis of bicyclic 1-arylpyrazol-5-ones

In this Letter, we described a facile method for constructing fused bicyclic 1-arylpyrazol-5-one ring system. We employed various methylene-containing carboxylic acids as the substrates and proved that the pyrazolone ring closure requires activated methylene group in intermediate II. Accordingly, a series of structurally diversified, fused bicyclic 1-arylpyrazol-5-ones was prepared in moderate to high yields using the requisite substrates.     

Synthesis of substituted 2,4,5,6-tetrahydrocyclopenta[c]pyrazoles and 2,4,5,6-tetrahydropyrrolo[3,4-c]pyrazoles by intramolecular nitrilimine cycloaddition

Both substituted 2,4,5,6-tetrahydrocyclopenta[c]pyrazoles and 2,4,5,6-tetrahydropyrrolo[3,4-c]pyrazoles have been synthesized by the 3+2 intramolecular dipolar cycloaddition of nitrilimines to alkynes. This cyclization has been extended to more versatile 3-bromo derivatives by the use of alkynylbromides as dipolarophiles.