763-89-3Relevant academic research and scientific papers
Oxidation of Isopropylcyclopropane by Chromyl Chloride: Ring-Opened Products Support a Hydrogen Atom Abstraction Mechanism
Wang, Kun,Mayer, James M.
, p. 4248 - 4252 (2007/10/03)
Chromyl chloride (CrO2Cl2) reacts with neat isopropylcyclopropane at 65 °C to give a dark precipitate along with at least 20 organic products. Both cyclopropyl products and ring-opened products are observed: 2-cyclopropyl-2-chloropropane (1,0.4% yield based on chromium), 2-cyclopropyl-2-propanol (2, 0.2%), 5-chloro-2-methyl-2-pentene (3, 0.3%), and 4-methyl-3-penten-1-ol (4, 0.5%) as well as other ring-opened products. Authentic samples of 1-4 were synthesized, and their GC and GC/ MS data were compared with the reaction mixture. Other organic products (5-10) were tentatively assigned by GC/MS on the basis of their m / z and fragmentation patterns. The ratio of (1 + 2) vs (3 + 4) increases by a factor of 2 when the initial concentration of CrO2Cl2 increases from 0.3 to 1.12 M. The reaction was also carried out in the gas phase, and essentially all the products from the liquid phase reaction were observed. The products are explained by a mechanism involving initial hydrogen atom abstraction from the substrate. The resulting dimethylcyclopropylcarbinyl radical can either be trapped by CrO2Cl2 (to form 1 and 2) or ring-open to give 4-methyl-3-pentenyl radical, which reacts with CrO2Cl2 to form 3 and 4 as well as further oxidized products. The oxidation of isopropylcyclopropane by MnO4- in pyridine was also examined. Acetone, an expected ring-opened product, was the only product observed by our analytical techniques. Me2C18O is produced from 18O-labeled MnO4-. These results suggest that the reactions of CrO2Cl2 and MnO4- with isopropylcyclopropane proceed by hydrogen atom transfer to form organic radical intermediates.
Intramolecular trapping of an ylide intermediate in the reaction of1:CH2 with an allylic alcohol
Sobery, Warunee,DeLuca, Joann P.
, p. 3315 - 3316 (2007/10/02)
The reaction of 1:CH2, generated by the photolysis of CH2N2, with 2-methyl-3-buten-2-ol leads to the formation of several products including 4-methyl-3-penten-1-ol. This product is best explained as the result of rearrangement of an ylide intermediate.
Nitro alkanes in organic synthesis: An efficient stereoselective synthesis of (+)-trans whisky lactone and (+)-eldanolide from nitro alkane synthons and using bakers' yeast reduction as the key step
Sarmah, Bhabani K.,Barua, Nabin C.
, p. 2253 - 2260 (2007/10/02)
An efficient route using nitroalkane synthon 3a and 3b for the synthesis of optically pure R-(+)-trans whisky lactone, (+)-9 and R-(+)-eldanolide, (+)-10 is described. In a key step, bakers' yeast reduction is employed to get the required chirality.
BASIC ELIMINATION OF SULFONIUM SALTS. NEIGHBOURING GROUP INFLUENCE ON REGIOSELECTIVITY.
Badet, B.,Julia, M.,Mallet, J. M.,Schmitz, C.
, p. 4331 - 4334 (2007/10/02)
A simple preparation of sulfonium salts functionalized by oxygenated groups is reported.The nature and the position of the latter control the regiochemistry of elimination of the sulfonium moiety leading to selective formation of Saytsev or Hofmann olefins.
