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Phosphonomethylation of cyclohexene oxides
The Journal of Organic Chemistry, 1993The tradeoff between synthetic directness and regioselectivity during oxirane ring opening is examined for two strategies used to phosphonomethylate cyclohexene oxide and substituted cyclohexene oxides derived from quinic acid and myo-inositol. Direct phosphonomethylation of the cyclohexene oxides utilizes diisopropyl lithiomethanephosphonate ((C 3 H 7
Jean Luc Montchamp +2 more
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Biocenversion of cyclohexene derivatives
Applied Microbiology and Biotechnology, 1984Bioconversion of new methylcyclohexene derivatives with bulky side chains ending in aromatic or heteroaromatic rings by Streptomyces natalensis and Mycobacterium smegmatis results in monohydroxylation of the cyclohexene ring. Further oxidation of the hydroxyl group into a keto group is effected only with M. smegmatis.
I. Belič +3 more
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Ultrafast Dynamics of Cyclohexene and Cyclohexene-d10 Excited at 200 nm
Journal of the American Chemical Society, 2001By exciting cyclohexene in the gas phase at 200 nm and probing it by nonresonant multiphoton ionization with mass-selective detection of the ion yields, we found four time constants tau(i) (20, 47, 43, 350 fs). Whereas deuteration lengthens tau2 by a factor of 1.4, the other constants do not change.
W, Fuss, W E, Schmid, S A, Trushin
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THE RADIOLYSIS OF CYCLOHEXANE: II. CYCLOHEXANE–CYCLOHEXENE SOLUTIONS AND PURE CYCLOHEXENE
Canadian Journal of Chemistry, 1960The γ-radiolysis of cyclohexane–cyclohexene solutions and of pure cyclohexene has been investigated. The previously determined yields of the two activated species in irradiated cyclohexane have been confirmed. G(c-C6H12′′) = 3.0 ± 0.3 and G(c-C6H12′) = 2.4 ± 0.3.The yields of the main products of cyclohexene radiolysis are G(H2) = 1.2, G(c-C6H12) = 1 ...
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THE AMMONOMERCURATION OF CYCLOHEXENE
Canadian Journal of Chemistry, 1965not available
D. Chow, J. H. Robson, George F Wright
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2001
(1; R = 1-pyrrolidino) [1125-99-1] C10H17N (MW 151.28) InChI = 1S/C10H17N/c1-2-6-10(7-3-1)11-8-4-5-9-11/h6H,1-5,7-9H2 InChIKey = KTZNVZJECQAMBV-UHFFFAOYSA-N (2; R = 4-morpholino) [670-80-4] C10H17NO (MW 167.28) InChI = 1S/C10H17NO/c1-2-4-10(5-3-1)11-6-8-12-9-7-11/h4H,1-3,5-9H2 InChIKey = IIQFBBQJYPGOHJ-UHFFFAOYSA-N (3; R = 1 ...
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(1; R = 1-pyrrolidino) [1125-99-1] C10H17N (MW 151.28) InChI = 1S/C10H17N/c1-2-6-10(7-3-1)11-8-4-5-9-11/h6H,1-5,7-9H2 InChIKey = KTZNVZJECQAMBV-UHFFFAOYSA-N (2; R = 4-morpholino) [670-80-4] C10H17NO (MW 167.28) InChI = 1S/C10H17NO/c1-2-4-10(5-3-1)11-6-8-12-9-7-11/h4H,1-3,5-9H2 InChIKey = IIQFBBQJYPGOHJ-UHFFFAOYSA-N (3; R = 1 ...
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