A Family of Highly Efficient CuI-Based Lighting Phosphors Prepared by a Systematic, Bottom-up Synthetic Approach

2015 ◽  
Vol 137 (29) ◽  
pp. 9400-9408 ◽  
Author(s):  
Wei Liu ◽  
Yang Fang ◽  
George Z. Wei ◽  
Simon J. Teat ◽  
Kecai Xiong ◽  
...  
Synthesis ◽  
2020 ◽  
Author(s):  
Peter Wipf ◽  
Thanh T. Nguyen

AbstractThe development of the intramolecular Diels–Alder cycloaddition­ of azole heterocycles, i.e. oxazoles (IMDAO), imidazoles (IMDAI), and thiazoles (IMDAT), has had a significant impact on the efficient preparation of heterocyclic intermediates and natural products. In particular, highly efficient and versatile IMDAO reactions have been utilized as a key step in several synthetic schemes to provide alkaloids and terpenoid target molecules. More limited studies have been performed on IMDAI and IMDAT cycloadditions. Some drawbacks, such as the occasionally­ challenging preparation of IMDA precursors, are also highlighted in this review. Perspectives are provided on how IMDAI and IMDAT­ transformations can be further expanded for target-directed syntheses.1 Introduction2 Oxazoles2.1 IMDAO Approaches to Furanosesquiterpenes and Furanosteroids2.1.1 Syntheses of Highly Oxygenated Sesquiterpenes2.1.2 Syntheses of (±)-Gnididione and (±)-Isognididione2.1.3 Synthesis of (±)-Stemoamide2.1.4 Synthesis of (±)-Paniculide A2.1.5 Syntheses of (+)- and (–)-Norsecurinine2.1.6 Synthesis of Evodone2.1.7 Syntheses of (±)-Ligularone and (±)-Petasalbine2.1.8 Syntheses of Imerubrine, Isoimerubrine, and Grandirubrine2.1.9 Syntheses of Furanosteroids2.1.10 Syntheses of Substituted Indolines and Tetrahydroquinolines2.2 IMDAO Approaches to Pyridines: the Kondrat’eva Reaction2.2.1 Syntheses of Suaveoline and Norsuaveoline2.2.2 Synthesis of Eupolauramine2.2.3 Syntheses of (–)-Plectrodorine and (+)-Oxerine2.2.4 Synthesis of Amphimedine2.2.5 Synthetic Approach to the Western Segment of Haplophytine2.2.6 Synthesis of Marinoquinoline A2.2.6.1 IMDAO Approach to Marinoquinoline A2.2.6.2 Scope of Allenyl IMDAO Cycloaddition2.3 Lewis Acid Catalysis in IMDAO Reactions2.3.1 Effects of Europium Catalysts on IMDAO Reactions2.3.2 Effects of Copper Catalysts on IMDAO Reactions3 Imidazoles 4 Thiazoles4.1 Syntheses of Menthane and Eremophilane4.2 Further Comments on the Intramolecular Cycloadditions of Thiocarbonyl Ylides5 Conclusions and Outlook


RSC Advances ◽  
2017 ◽  
Vol 7 (1) ◽  
pp. 408-414 ◽  
Author(s):  
Chang-An Wang ◽  
Yan-Wei Li ◽  
Xue-Li Cheng ◽  
Jian-Ping Zhang ◽  
Yin-Feng Han

Eosin Y dye has been successfully embedded into a nanoporous network EY-POPs through a bottom-up strategy. The polymers could be used as highly effective and reusable heterogeneous organo-photocatalyst for the dehydrogenative coupling reaction.


2018 ◽  
Vol 57 (21) ◽  
pp. 13912-13919 ◽  
Author(s):  
Changda Li ◽  
Haitong Tang ◽  
Yu Fang ◽  
Zhifeng Xiao ◽  
Kunyu Wang ◽  
...  

2020 ◽  
Vol 10 (15) ◽  
pp. 5171-5180
Author(s):  
Wan-Kai An ◽  
Shi-Jia Zheng ◽  
Ya-Nan Du ◽  
San-Yuan Ding ◽  
Zhi-Jun Li ◽  
...  

“Bottom-up” embedding of thiophene derivatives into CMPs for highly efficient heterogeneous photocatalysis is reported.


2016 ◽  
Vol 12 ◽  
pp. 524-530 ◽  
Author(s):  
Mária Mastihubová ◽  
Monika Poláková

Several bioactive natural p-hydroxyphenylalkyl β-D-glucopyranosides, such as vanillyl β-D-glucopyranoside, salidroside and isoconiferin, and their glycosyl analogues were prepared by a simple reaction sequence. The highly efficient synthetic approach was achieved by utilizing acetylated glycosyl bromides as well as aromatic moieties and mild glycosylation promoters. The aglycones, p-O-acetylated arylalkyl alcohols, were prepared by the reduction of the corresponding acetylated aldehydes or acids. Various stereoselective 1,2-trans-O-glycosylation methods were studied, including the DDQ–iodine or ZnO–ZnCl2 catalyst combination. Among them, ZnO–iodine has been identified as a new glycosylation promoter and successfully applied to the stereoselective glycoside synthesis. The final products were obtained by conventional Zemplén deacetylation.


Biomaterials ◽  
2015 ◽  
Vol 39 ◽  
pp. 206-217 ◽  
Author(s):  
Shige Wang ◽  
Kai Li ◽  
Yu Chen ◽  
Hangrong Chen ◽  
Ming Ma ◽  
...  

Nanoscale ◽  
2020 ◽  
Vol 12 (21) ◽  
pp. 11435-11439
Author(s):  
Diogo A. Gálico ◽  
Jeffrey S. Ovens ◽  
Muralee Murugesu

Lanthanide molecular clusters as near-infrared markers are highly tunable owing to the bottom-up synthetic approach. Facile synthesis, high crystallinity, water stability are all highly desirable attributes of clusters for biological and telecommunications technology.


2019 ◽  
Vol 31 (40) ◽  
pp. 1903239 ◽  
Author(s):  
Ding Zheng ◽  
Ruixiang Peng ◽  
Gang Wang ◽  
Jenna Leigh Logsdon ◽  
Binghao Wang ◽  
...  

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