Results 61 to 70 of about 853 (100)
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Phosphonomethylation of cyclohexene oxides

The Journal of Organic Chemistry, 1993
The 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
openaire   +1 more source

Biocenversion of cyclohexene derivatives

Applied Microbiology and Biotechnology, 1984
Bioconversion 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
openaire   +1 more source

Ultrafast Dynamics of Cyclohexene and Cyclohexene-d10 Excited at 200 nm

Journal of the American Chemical Society, 2001
By 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
openaire   +2 more sources

THE RADIOLYSIS OF CYCLOHEXANE: II. CYCLOHEXANE–CYCLOHEXENE SOLUTIONS AND PURE CYCLOHEXENE

Canadian Journal of Chemistry, 1960
The 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, 1965
not available
D. Chow, J. H. Robson, George F Wright
openaire   +1 more source

1-Pyrrolidino-1-cyclohexene

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 ...
openaire   +1 more source

Cyclohexene

2014
S. Mostafalou, H. Bahadar
openaire   +1 more source

A trans cyclohexene

Journal of the American Chemical Society, 1976
R. Bonneau   +3 more
openaire   +1 more source

Polymerisation of cyclohexene

Recueil des Travaux Chimiques des Pays-Bas, 1935
H. I. Waterman   +2 more
openaire   +1 more source

C6H10, Cyclohexene

2005
G. Graner   +6 more
openaire   +1 more source

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