Regioselective synthesis and zone selective deprotection of [60]fullerene tris-adducts with an e,e,e addition pattern

Literature Information

Publication Date 2005-06-16
DOI 10.1039/B504748J
Impact Factor 6.222
Authors

Florian Beuerle, Nikos Chronakis, Andreas Hirsch


View Original

Abstract

D 3h-symmetrical tripodal tris(malonate) tethers have been used for the synthesis of [60]fullerene tris-adducts with an e,e,e addition pattern bearing topologically distinct polar and equatorial addend zones that can selectively be deprotected.

Related Literature

Carbon atom insertion into N-heterocyclic carbenes to yield 3,4-dihydroquinoxalin-2(1H)-ones

Justin S. Lamb, Futa Koyama, Noriyuki Suzuki, Yumiko Suzuki

2023-11-10 Research Article

DOI: 10.1039/D3QO01579C

Pulsed electrolysis: enhancing primary benzylic C(sp3)–H nucleophilic fluorination

Alexander P. Atkins, Atul K. Chaturvedi, Joseph A. Tate, Alastair J. J. Lennox

2023-12-13 Research Article

DOI: 10.1039/D3QO01865B

Visible light photoredox-catalyzed deoxydisulfuration of alcohols

Chaoyang Liu, Xiaoman Lin, Delie An

2023-11-22 Research Article

DOI: 10.1039/D3QO01742G

Photocatalytic formation of P–S bonds via CdSeS/CdZnS quantum dots under visible light irradiation

Zi-Jun Lei, Yue-Yue Zhang, Hui-Ling Lu, Fu-Gang Zhao, Jian-Hai Zhou, Xiaogang Peng

2023-11-23 Research Article

DOI: 10.1039/D3QO01560B

Genome-driven discovery of new serrawettin W2 analogues from Serratia fonticola DSM 4576

Haolin Qiu, Yang Xiao, Ling Shen, Tao Han, Qiang He, Aiying Li, Peng Zhang

2023-10-31 Paper

DOI: 10.1039/D3OB01642K

Transition metal free C(sp3)–C(sp3) coupling between alcohols and N-heteroarenes via a dehydrogenative SET/HAT process

Xiaoping Liu, Dongjie Wang, Jordan Garo, Jean-Marc Sotiropoulos, Marc Taillefer

2023-12-12 Research Article

DOI: 10.1039/D3QO01875J

Back cover

2023-11-15 Cover

DOI: 10.1039/D3OB90164E

Correction: An efficient metal free synthesis of 2-aminobenzothiozoles – a greener approach

Ganesh Sambasivam, Govindarajulu Gavara, Ramraj S, Gaikwad Rajendra, Karthikeyan Sivashanmugam

2023-11-02 Correction

DOI: 10.1039/D3OB90143B

Asymmetric total synthesis of montanine-type amaryllidaceae alkaloids

Fang Wang, Xiaohan Xu, Yangtian Yan, Jiayang Zhang, Yang Yang

2023-12-03 Research Article

DOI: 10.1039/D3QO01835K

Electrochemical (radio)-halodesilylation of aromatic silanes

Kehao Gong, Long Lin, Xinyan Gao, Xiaojun Zeng, Bo Xu, Junbin Han

2023-11-24 Research Article

DOI: 10.1039/D3QO01553J

You might also like

Compound Q&A

How should 2-Methylbenzene-1,4-diamine dihydrochloride (CAS: 615-45-2) be stored?

2-Methylbenzene-1,4-diamine dihydrochloride (CAS: 615-45-2) should be stored in ...

615-45-22-Methylbenzene-1,4-...
Compound Q&A

Is (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide (CAS: 132747-20-7) safe?

(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide is generally considered sa...

132747-20-7(1S,4S)-2,5-Diazabic...
Compound Q&A

What industries use (6-Chloropyridazin-3-YL)methanamine (CAS: 871826-15-2)?

(6-Chloropyridazin-3-YL)methanamine finds applications in the pharmaceutical ind...

871826-15-2(6-Chloropyridazin-3...
Compound Q&A

What are the main uses of 2-Fluoro-3-methylphenol (CAS: 77772-72-6)?

2-Fluoro-3-methylphenol is primarily used in the synthesis of pharmaceuticals, p...

77772-72-62-Fluoro-3-methylphe...
Compound Q&A

What precautions should be taken when handling 3-Methoxy-4-nitrobenzonitrile (CAS: 177476-75-4)?

When handling 3-Methoxy-4-nitrobenzonitrile, it is important to wear appropriate...

177476-75-43-Methoxy-4-nitroben...
Compound Q&A

What precautions should be taken when handling 1,3-Oxazolo[4,5-b]pyridine-2(3H)-thione (CAS: 211949-57-4)?

When handling 1,3-Oxazolo[4,5-b]pyridine-2(3H)-thione (CAS: 211949-57-4), it is ...

211949-57-4[1,3]Oxazolo[4,5-b]p...
Compound Q&A

What regulatory guidelines apply to 4-Ethynylbenzamide (CAS: 90347-86-7)?

4-Ethynylbenzamide (CAS: 90347-86-7) falls under various regulatory guidelines i...

90347-86-74-Ethynylbenzamide
Compound Q&A

What are the main uses of 3-(2-Ethylphenyl)-2-thioxo-4-imidazolidinone (CAS: 186822-57-1)?

3-(2-Ethylphenyl)-2-thioxo-4-imidazolidinone is primarily used as an intermediat...

186822-57-13-(2-Ethylphenyl)-2-...
Compound Q&A

What is (2-Fluoro-6-methoxyphenyl)acetic acid (CAS: 500912-19-6)?

(2-Fluoro-6-methoxyphenyl)acetic acid, also known as 4-fluoro-3-methoxybenzoic a...

500912-19-6(2-Fluoro-6-methoxyp...
Compound Q&A

What is the market or research trend for 2-[4-(Hydroxymethyl)phenoxy]ethanol (CAS: 102196-18-9)?

Market trends for 2-[4-(Hydroxymethyl)phenoxy]ethanol (CAS: 102196-18-9) indicat...

102196-18-92-[4-(Hydroxymethyl)...

Source Journal

Chemical Communications

Chemical Communications
CiteScore: 8.6
Self-citation Rate: 4.7%
Articles per Year: 2458

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

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.