Frans

Hennico, A., A. Billon, P.-H. Bigeard and J.-P. Peries (1993), IFP s new flexible hydrocracking process combines maximum conversion with production of high viscosity, high VI lube stocks . Rev. Inst. Fran. du Petrole, Vol. 48, No. 2, p. 127. 

Quivoron, C. (1978), "Thermodynamique des solutions de polymeres". In Initiation a la physicochimie macromoleculaire. Groupement Fran ais des Polymeres, Strasbourg. 

Association Fran aise de Normalisation Association Fran aise des Techniciens du Petrole i American Institute of Chemical Engineers i American National Standards Institute aniline point... 

Groupement Fran ais de Coordination pour le developpement des essais de performance des lubrifiants et des combustibles pour moteurs... 

C8Hi7CH=CH(CH2)7COOH Elaidic acid frans-9-Octadecenoic acid... 

C.K. Johnson, ONRL Report No. 3794, Oak Ridge National Laboratory, Oak Ridge, TN, 1965 abstract available at http //www.umass.edu/molvis/fran-coeur/ortep/ortepabstract.html [5 Ctfile Formats, MDL Information Systems, CA, 1998 http //www.mdli.com/ downloads... 

The addition of acetylides to oxiranes yields 3-alkyn-l-ols (F. Sondheimer, 1950 M.A. Adams, 1979 R.M. Carlson, 1974, 1975 K. Mori, 1976). The acetylene dianion and two a -synthons can also be used. 1,4-Diols with a carbon triple bond in between are formed from two carbonyl compounds (V. Jager, 1977, see p. 52). The triple bond can be either converted to a CIS- or frans-configurated double bond (M.A. Adams, 1979) or be hydrated to give a ketone (see pp. 52, 57, 131). 

D. Lowe, "Crisis Management Marketing, Tampering Strategies for International and Domestic Marketplace Terrorism," San Fran. St. Univ. J. 1, (1990). 

Thermal decomposition of cis- and frans-3,6-dimethyl-3,4,5,6-tetrahydropyridazines affords propene, cis- and frans-l,2-dimethylcyclobutanes and 1-hexene. The stereochemistry of the products is consistent with the intermediacy of the 1,4-biradical 2,5-hexadienyl. The results indicate that thermal reactions of cyclic azo compounds and cyclobutanes of similar substitution proceed with similar stereospecificity when compared at similar temperatures 79JA2069). 

In 1911 Heim observed that the reaction of two moles of phenylnitromethane and one mole of benzaldehyde in the presence of an aliphatic amine gave cis- and frans-nitrostilbenes and three other products. One of the products was triphenylisoxazole (11CB2016). In 1924 Kohler reinvestigated the reaction (24JA2105). He observed that the reaction of phenylnitromethane (367) and cfs-a-nitrostilbene (368) in the presence of sodium methoxide gave... 

N- Aminoaziridines have been converted to alkenes by reaction with a variety of oxidizing agents (70JA1784). Usually, the deamination reaction is stereospecific. The oxidation of l-amino-2,3-diphenylaziridines with manganese dioxide, however, was not stereospecific. The trans compound gives entirely frans-stilbene, whereas the cfs-aziridine forms a mixture of 85% trans- and 15% c -aikene. cw-Stilbene is not isomerized to trans under the reaction conditions, and the results are explained in terms of an azamine intermediate which can isomerize through a tautomeric equilibrium. 

Methyl-6-(W,/V-dimethylamino)-frans-4-nitro-frans-5-phenyl-cyclohexene... 

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