A peptide-catalyzed asymmetric Stetter reaction
Literature Information
Steven M. Mennen, Jarred T. Blank, Michelle B. Tran-Dubé, Jason E. Imbriglio, Scott J. Miller
Thiazolylalanine, in appropriately functionalized form, has been found to function as an enantioselective catalyst for an intramolecular Stetter reaction. Incorporation of the residue in a number of environments has resulted in a family of catalysts that promote the cyclization of a test substrate with up to 81% enantiomeric excess.
Recommended Journals
Related Literature
Synthesis of metallic magnesium nanoparticles by sonoelectrochemistry
Iris Haas, Aharon Gedanken
DOI: 10.1039/B717670H
Palladium-catalyzed three-component coupling of arynes with allylic acetates or halides and terminal alkynes promoted by cuprous iodide
Sivakolundu Bhuvaneswari, Masilamani Jeganmohan, Ming-Che Yang, Chien-Hong Cheng
DOI: 10.1039/B800118A
Nucleophilicities and carbon basicities of DBU and DBN‡
M. Baidya, Herbert Mayr
DOI: 10.1039/B801811A
Synthesis of iron oxide nanoparticles in a microfluidic device: preliminary results in a coaxial flow millichannel
Ali Abou Hassan, Olivier Sandre, Valérie Cabuil, Patrick Tabeling
DOI: 10.1039/B719550H
Clean and efficient synthesis of O-silylcarbamates and ureas in supercritical carbon dioxide
Matthew J. Fuchter, Catherine J. Smith, Alistair Boyer, Simon Saubern, John H. Ryan, Andrew B. Holmes
DOI: 10.1039/B801537F
A practical demonstration of electronic promotion in the reduction of ceria coated PGM catalysts
Shik Chi Tsang, Stan Golunski, Paul Collier
DOI: 10.1039/B718956G
Single molecule conformational analysis of the biologically relevant DNA G-quadruplex in the promoter of the proto-oncogene c-MYC
Pravin S. Shirude, Liming Ying, Shankar Balasubramanian
DOI: 10.1039/B801465E
A novel mediator–polymer-modified anode for microbial fuel cells
Masanori Adachi, Tatsuo Shimomura, Makoto Komatsu, Hiroshi Yakuwa, Akiko Miya
DOI: 10.1039/B717773A
Pressure effects and Mössbauer spectroscopic studies on a 3D mixed-valence iron spin-crossover complex with NiAs topology
Yue-Ling Bai, Jun Tao, Rong-Bin Huang, Lan-Sun Zheng, Shao-Liang Zheng, Kazuyoshi Oshida, Yasuaki Einaga
DOI: 10.1039/B718456E
You might also like
What precautions should be taken when handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3)?
When handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3), it ...
What precautions should be taken when handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9)?
When handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9), it...
How should waste containing 2-[2-(2-Methoxyethoxy)ethoxy]ethyl 4-methylbenzenesulfonate (CAS: 62921-74-8) be handled?
Waste containing this compound (CAS: 62921-74-8) should be handled according to ...
How should waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate be handled?
Waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate should be collected i...
How is 5-({4-[(2S,4R)-4-Hydroxy-2-methyltetrahydro-2H-pyran-4-yl]-2-thienyl}sulfanyl)-1-methyl-1,3-dihydro-2H-indol-2-one (CAS: 166882-70-8) typically synthesized?
This compound can be synthesized using a multi-step process involving the conjug...
Are there alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid (CAS: 7312-27-8) in synthesis?
There are several alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid in syn...
How should Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84-9) be stored?
Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84...
How should waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) be handled?
Waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) should be coll...
How is Methyl 5-iodo-2-methylbenzoate (CAS: 103440-54-6) typically synthesized?
Methyl 5-iodo-2-methylbenzoate can be synthesized through the iodination of meth...
How is 5-Chloro[1,2,4]triazolo[1,5-a]pyridine (CAS: 1427399-34-5) typically synthesized?
5-Chloro[1,2,4]triazolo[1,5-a]pyridine is commonly synthesized via the condensat...
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














