The quest for secondary structure in chiral dendrimers
Literature Information
Susan E. Gibson, Jacob T. Rendell
This review highlights important developments in the pursuit of chiral conformational order in dendritic structures. To be able to create and control chiral secondary structure necessitates a thorough understanding of how chiral subunits influence the macroscopic structure. Recent studies involve highly sophisticated manipulation of macroscopic chirality through a creative combination of a wide range of synthetic, computational and analytical techniques.
Related Literature
Single layer growth of sub-micron metal–organic framework crystals observed by in situatomic force microscopy
Neena S. John, Camilla Scherb, Maryiam Shöâeè, Michael W. Anderson, Martin P. Attfield, Thomas Bein
DOI: 10.1039/B908299A
Easy preparation of a reticular nickel film deposited on a barrel-plating gold electrode with a high catalytic activity towards the oxidation of glucose
Chun-Yen Tai, Jen-Lin Chang, Jyh-Myng Zen
DOI: 10.1039/B912442J
Radical generation from electroreduction of aryl and benzyl ammonium salts: synthesis of organoboronates
Long Lin, Qianjin Chen, Bo Xu
DOI: 10.1039/D0QO00979B
Application of REDORNMR in natural product chemistry
Shigeru Matsuoka, Masayuki Inoue
DOI: 10.1039/B910230B
Diphenylamine end-capped 1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrrole (DPP) derivatives with large two-photon absorption cross-sections and strong two-photon excitation red fluorescence
Er Qian Guo, Pei Hua Ren, Yan Li Zhang, Hai Chang Zhang, Wen Jun Yang
DOI: 10.1039/B911808J
Photocatalytic intramolecular radical cyclization involved synergistic SET and HAT: synthesis of 3,3-difluoro-γ-lactams
Xiaohui Zhuang, Xiayue Shi, Rui Zhu, Bin Sun
DOI: 10.1039/D0QO01188F
Triarylamine: a promising core unit for efficient photovoltaic materials
Zhijun Ning, He Tian
DOI: 10.1039/B908802D
Rh(iii)-Catalyzed switchable C–H monoalkenylation and dialkenylation of 2-(1H-pyrazol-1-yl)pyridine with alkenes via rollover cyclometalation
Haifang Meng, Fang Yang, Mengjia Chen, Chen Chen, Bolin Zhu
DOI: 10.1039/D0QO01325K
Dual reactivity of a photochemically-generated cyclic enyne–allene
Alexander V. Kuzmin, Vladimir V. Popik
DOI: 10.1039/B911871C
You might also like
Are there alternatives to 1-(4-Chlorophenyl)-N-hydroxymethanimine (CAS: 3848-36-0) in synthesis?
When considering alternatives to 1-(4-Chlorophenyl)-N-hydroxymethanimine (CAS: 3...
How should (1R,9S,10S,12S,14E,16S,19R,20R,21S,22R)-3,9,21-Trihydroxy-5,10,12,14,16,20,22-heptamethyl-23,24-dioxatetracyclo[17.3.1.1~6,9~.0~2,7~]tetracosa-2,5,7,14-tetraen-4-one (CAS: 183202-73-5) be stored?
This compound should be stored in a cool, dry place away from direct sunlight. I...
How is 3-(4-Bromophenyl)-5-(2-fluorophenyl)-1,2,4-oxadiazole (CAS: 419553-16-5) typically synthesized?
3-(4-Bromophenyl)-5-(2-fluorophenyl)-1,2,4-oxadiazole is synthesized through a m...
How is 5-Chloro-2-(4-chlorophenyl)-4-methyl-6-[3-(1-piperidinyl)propoxy]pyrimidine (CAS: 1639220-19-1) typically synthesized?
5-Chloro-2-(4-chlorophenyl)-4-methyl-6-[3-(1-piperidinyl)propoxy]pyrimidine (CAS...
What industries use 2-Chloro-4-(difluoromethoxy)pyridine (CAS: 1206978-15-5)?
2-Chloro-4-(difluoromethoxy)pyridine is used in the pharmaceutical industry for ...
What regulatory guidelines apply to 3-Chloro-6-methylpyridazine (CAS: 1121-79-5)?
3-Chloro-6-methylpyridazine (CAS: 1121-79-5) is classified under the Globally Ha...
Are there alternatives to Methyl 4,5-dimethyl-2-nitrobenzoate in synthesis?
Several alternatives can be used in the synthesis of Methyl 4,5-dimethyl-2-nitro...
Are there alternatives to (2E,2'E)-3,3'-(1,4-Phenylene)bisacrylaldehyde in synthesis?
Alternatives to (2E,2'E)-3,3'-(1,4-Phenylene)bisacrylaldehyde include other acry...
What is 3-Amino-5-chloropyridin-2-ol hydrochloride (CAS: 1261906-29-9)?
3-Amino-5-chloropyridin-2-ol hydrochloride is an organic compound with the CAS n...
What precautions should be taken when handling 6,7-Difluoro-2,3-dihydro-4H-chromen-4-one (CAS: 1092349-93-3)?
When handling 6,7-Difluoro-2,3-dihydro-4H-chromen-4-one, it is essential to wear...
Source Journal
Chemical Communications

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry












![[4-(Isobutyrylamino)phenyl]boronic acid structure [4-(Isobutyrylamino)phenyl]boronic acid structure](https://static.chemtradehub.com/structs/874/874219-50-8-6ab5.webp)

