Oligosilylated group 4 titanocenes in the oxidation state +3
Literature Information
Michaela Zirngast, Ulrich Flörke, Judith Baumgartner, Christoph Marschner
Reactions of oligosilylanions with Cp2TiCl2 led to the formation of ate-complexes of silylated titanocenes, which form upon silylation of the intermediate K[Cp2TiCl2]·18-crown-6.
Recommended Journals
Related Literature
Hydroxylation of benzophenone with ammonium phosphomolybdate in the solid state via UV photoactivation
Mrinmoyee Basu, Suresh Sarkar, Surojit Pande, Subhra Jana, Arun Kumar Sinha, Sougata Sarkar, Mukul Pradhan, Anjali Pal, Tarasankar Pal
DOI: 10.1039/B905718H
Reusable polystyrene-supported Pdcatalyst for Mizoroki–Heck reactions with extremely low amounts of supported Pd
Carine Diebold, Stéphane Schweizer, Jean-Michel Becht, Claude Le Drian
DOI: 10.1039/C0OB00523A
Controlled growth of novel hyper-branched nanostructures in nanoporous alumina membrane
Junping Zhang, Cynthia S. Day, David L. Carroll
DOI: 10.1039/B913917F
Redox rich dicobalt macrocycles as templates for multi-electron transformations
Nathaniel K. Szymczak, Louise A. Berben, Jonas C. Peters
DOI: 10.1039/B913946J
Facile synthesis of 1,3,4-benzotriazepines and 1-arylamide-1H-indazoles viapalladium-catalyzed cyclization of aryl isocyanates and aryl hydrazones under microwave irradiation
Chune Dong, Lingli Xie, Xiaohong Mou, Yashan Zhong, Wei Su
DOI: 10.1039/C0OB00021C
Acid–base properties of functionalised tripodal polyamines and their interaction with nucleotides and nucleic acids
Alejandra Sornosa-Ten, M. Teresa Albelda, Juan C. Frías, Enrique García-España, José M. Llinares, Ana Budimir, Ivo Piantanida
DOI: 10.1039/C000124D
Efficient synthesis of a hetero[4]rotaxane by a “threading-stoppering-followed-by-clipping” approach
Jun Yin, Chunyan Chi, Jishan Wu
DOI: 10.1039/C001343A
Electrochemistry at carbon nanotubes: perspective and issues
Ioana Dumitrescu, Patrick R. Unwin, Julie V. Macpherson
DOI: 10.1039/B909734A
Design of one-to-one recognition triple Au nanoparticlesDNA probe and its application in the electrochemical DNAbiosensor
Hua Zhong, Xi Lei, Xu Hun, Shusheng Zhang
DOI: 10.1039/B913922B
You might also like
What industries use (1R,3S)-1,3-Cyclopentanediol (CAS: 16326-97-9)?
(1R,3S)-1,3-Cyclopentanediol finds applications in various industries. In the ph...
What precautions should be taken when handling N'-[4-(Dimethylamino)phenyl]-N,N-dimethyl-1,4-benzenediamine (CAS: 637-31-0)?
When handling N'-[4-(Dimethylamino)phenyl]-N,N-dimethyl-1,4-benzenediamine, it i...
Are there alternatives to 5-(2,4-Difluorophenyl)-2-methoxypyrimidine (CAS: 1352318-16-1) in synthesis?
There are several alternatives to 5-(2,4-Difluorophenyl)-2-methoxypyrimidine in ...
What regulatory guidelines apply to 1-(3-Methoxyphenoxy)propan-2-ol (CAS: 382141-68-6)?
1-(3-Methoxyphenoxy)propan-2-ol (CAS: 382141-68-6) must comply with the Globally...
Is Tetrodotoxin Citrate (CAS: 18660-81-6) safe?
Tetrodotoxin Citrate is extremely dangerous and should be handled with extreme c...
What are the main uses of 2-Methyl-2-propanyl [(1R,3S)-3-hydroxycyclopentyl]carbamate (CAS: 225641-84-9)?
2-Methyl-2-propanyl [(1R,3S)-3-hydroxycyclopentyl]carbamate (CAS: 225641-84-9) i...
How should waste containing 4-(2-Hydroxyhexafluoroisopropyl)Benzoic Acid (CAS: 16261-80-6) be handled?
Waste containing 4-(2-Hydroxyhexafluoroisopropyl)Benzoic Acid (CAS: 16261-80-6) ...
How is 2-Methyl-2-proanyl {(2S)-1-[(benzyloxy)amino]-3-hydroxy-3-methyl-1-oxo-2-butanyl}carbamate (CAS: 102507-19-7) typically synthesized?
2-Methyl-2-proanyl {(2S)-1-[(benzyloxy)amino]-3-hydroxy-3-methyl-1-oxo-2-butanyl...
What is Benzeneethanamine, α-ethyl-, hydrochloride (1:1) (CAS: 20735-15-3)?
Benzeneethanamine, α-ethyl-, hydrochloride (1:1) is an organic compound with the...
Are there alternatives to 3-{(E)-[4-(Dimethylamino)phenyl]diazenyl}benzoic acid (CAS: 20691-84-3) in synthesis?
In the synthesis of compounds similar to 3-{(E)-[4-(Dimethylamino)phenyl]diazeny...
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













![(2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-(methylselanyl)butanoic acid structure (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-(methylselanyl)butanoic acid structure](https://static.chemtradehub.com/structs/121/1217852-49-7-f252.webp)
