✦ LIBER ✦

(Aryltelluro)formates as Precursors of Alkyl Radicals: Thermolysis and Photolysis of Primary and Secondary Alkyl (Aryltelluro)formates

✍ Scribed by Lucas, Mathew A.; Schiesser, Carl H.

Book ID: 121445159
Publisher: American Chemical Society
Year: 1996
Tongue: English
Weight: 348 KB
Volume: 61
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo960838y

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: (Aryltelluro)format

ChemInform Abstract: (Aryltelluro)formates as Precursors of Alkyl Radicals: Thermolysis and Photolysis of Primary and Secondary Alkyl (Aryltelluro)formates.

✍ M. A. LUCAS; C. H. SCHIESSER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

ChemInform Abstract: Efficient Formation

ChemInform Abstract: Efficient Formation of H-Addition Radical and Secondary Alkyl Radical in Pentylthymines (I) γ-Irradiated at 77 K.

✍ Nobuaki Ohta; Noriyuki Tanaka; Sotaro Ito 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB

Product Studies and Laser Flash Photolys

Product Studies and Laser Flash Photolysis on Alkyl Radicals Containing Two Different β-Leaving Groups Are Consonant with the Formation of an Olefin Cation Radical

✍ Bales, Brian C.; Horner, John H.; Huang, Xianhai; Newcomb, Martin; Crich, David; 📂 Article 📅 2001 🏛 American Chemical Society 🌐 English ⚖ 107 KB

Alkyl nitrate formation from the reactio

Alkyl nitrate formation from the reaction of a series of branched RO2radicals with NO as a function of temperature and pressure

✍ Roger Atkinson; Sara M. Aschmann; Arthur M. Winer 📂 Article 📅 1987 🏛 Springer Netherlands 🌐 English ⚖ 528 KB

Alkyl nitrate yields from the NO x photooxidations of neopentane, 2-methylbutane and 3-methylpentane have been determined over the temperature and pressure ranges 281-323 K and 54-740 tort, respectively. The formation of the alkyl nitrates is attributed to the reaction pathway and rate constant rat

Pseudoesters and Derivatives. XXVII. The

Pseudoesters and Derivatives. XXVII. Thermolysis and Photolysis of Cyclozdducts of Diazomethane with 5-Methoxy-3-pyrrolin-2-ones. Formation of 4-Alkyl-3-pyrrolin-2-ones and 3-Azabicyclo[3.1.0]hexan-2-ones

✍ Fariña, Francisco; Victoria Mart地, M.; Carmen Paredes, M.; Tito, Ameria 📂 Article 📅 1988 🏛 Japan Institute of Heterocyclic Chemistry 🌐 English ⚖ 140 KB

[Ir(COD)Cl] 2 as a Catalyst Precursor fo

[Ir(COD)Cl] 2 as a Catalyst Precursor for the Intramolecular Hydroamination of Unactivated Alkenes with Primary Amines and Secondary Alkyl- or Arylamines: A Combined Catalytic, Mechanistic, and Computational Investigation

✍ Hesp, Kevin D.; Tobisch, Sven; Stradiotto, Mark 📂 Article 📅 2010 🏛 American Chemical Society 🌐 English ⚖ 846 KB