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Surrogates for chiral aminomalondialdehyde: synthesis of N-(9-phenylfluoren-9-yl)serinal and N-(9-phenylfluoren-9-yl)vinylglycinalLUBELL, W; RAPOPORT, H.Journal of organic chemistry. 1989, Vol 54, Num 16, pp 3824-3831, issn 0022-3263, 8 p.Article

Phase Segregation and Gas Separation Properties of Thermally Treated Copoly(ether-imide) from an Aromatic Dianhydride, an Aromatic Diamine, and Various Aliphatic DiaminesTENA, Alberto; MARCOS-FERNANDEZ, Angel; PALACIO, Laura et al.Industrial & engineering chemistry research. 2012, Vol 51, Num 9, pp 3766-3775, issn 0888-5885, 10 p.Article

Chemical decomposition of chlorofluorocarbons by reductive dehalogenation using sodium naphthalenideOKU, A; KIMURA, K; SATO, M et al.Chemistry Letters. 1988, Num 10, pp 1789-1792, issn 0366-7022Article

Anaerober Abbau von Kohlenwasserstoffen = Anaerobic degradation of hydrocarbonsSCHINK, B.Erdöl und Kohle, Erdgas, Petrochemie. 1989, Vol 42, Num 3, pp 116-118, issn 0014-0058, 3 p.Article

Umlagerung von Dehydrolinalool zu Citral und von Linaloo zu Geraniol = Passage du déhydrolinalool au citral et du linalool au géraniol = The rearrangement of dehydrolinalool to citral and of linalool to geraniolCERVENY, L; RUZICKA, V.Parfümerie und Kosmetik. 1988, Vol 69, Num 1, pp 9-16, issn 0031-1952, 5 p.Article

Synthesis and reactivity of lithiated γ-functionalised ketene dithioacetals. Generation of a flexible β-lithioacrylate equivalentDZIADULEWICZ, E; HODGSON, D; GALLAGHER, T et al.Journal of the Chemical Society. Perkin transactions. I. 1988, Num 12, pp 3367-3373, issn 0300-922XArticle

Carbon spheres generated in 'dusty plasmas'CHEN, G. Y; STOLOJAN, V; SILVA, S. R. P et al.Carbon (New York, NY). 2005, Vol 43, Num 4, pp 704-708, issn 0008-6223, 5 p.Article

1-(Pentafluoro-λ⁶-sulfanyl)2,2,2-trifluoroethanethione, F₅S(F₃C)C=S, and related compoundsKUSCHEL, R; SEPPELT, K.Inorganic chemistry (Print). 1993, Vol 32, Num 16, pp 3568-3569, issn 0020-1669Article

Synthesis of sorbistin analoguesMEDGYES, G; JERKOVICH, G; KUSZMANN, J et al.Carbohydrate research. 1989, Vol 186, Num 2, pp 225-239, issn 0008-6215, 15 p.Article

Decomposition of nitrogen-containing organic compounds in electrical dischargesPETRUSENKO, A. P; PESIN, O. YU; PECHURO, N. S et al.Himičeskaâ promyšlennost'. 1989, Num 9, pp 656-659, issn 0023-110X, 4 p.Article

Electrophilic amination: enantioselective syntheses of D-allothreonine and L-threonineGENET, J. P; JUGE, S; MALLART, S et al.Tetrahedron letters. 1988, Vol 29, Num 51, pp 6765-6768, issn 0040-4039Conference Paper

Biosynthetic studies on validamycins: a C₂+C₂C₃ pathway to an aliphatic C₇N unitTOYOKUNI, T; WEN-ZAO JIN; RINEHART, K. L. JR et al.Journal of the American Chemical Society. 1987, Vol 109, Num 11, pp 3481-3482, issn 0002-7863Article

Synthesis of S-methyl 2-hydroxyalkanethioates, 2-hydroxyalkanoic acids and related compounds via the addition reaction of tris(methylthio)methanide ion to alkanalsORITO, K; SEKI, Y; SUGINOME, H et al.Bulletin of the Chemical Society of Japan. 1989, Vol 62, Num 6, pp 2013-2017, issn 0009-2673, 5 p.Article

Synthesis and hydrosilylation reactions of allyl methacrylateSAXENA, A. K; BISARIA, C. S; PANDE, L. M et al.Indian journal of technology. 1991, Vol 29, Num 6, pp 310-312, issn 0019-5669Article

Synthese und Eigenschaften von Nα-Di-tert-butoxycarbonyl- und Nα-Benzyloxycarbonyl-tert-butoxycarbonyl-aminosäuren = Synthèse et propriétés de Nα-di-t-butoxycarbonyl- et Nα-benzyloxycarbonyl t-butoxycarbonyl aminoacides = Synthesis and properties of Nα-di-t-butoxycarbonyl- and Nα-benzyloxycarbonyl-t-butoxycarbonyl-aminoacidsGUNNARSSON, K; GREHN, L; RAGNARSSON, U et al.Angewandte Chemie. 1988, Vol 100, Num 3, pp 411-412, issn 0044-8249Article

Fragrance material review on ethylene dodecanedioateMCGINTY, D; LETIZIA, C. S; API, A. M et al.Food and chemical toxicology. 2011, Vol 49, issn 0278-6915, S212-S218, SUP2Article

Combinatorial models and algorithms in chemistry. The expanded Wiener number : a novel topological indexTRATCH, S. S; STANKEVITCH, M. I; ZEFIROV, N. S et al.Journal of computational chemistry. 1990, Vol 11, Num 8, pp 899-908, issn 0192-8651, 10 p.Article

Fragrance material review on ethylene brassylateMCGINTY, D; LETIZIA, C. S; API, A. M et al.Food and chemical toxicology. 2011, Vol 49, issn 0278-6915, S174-S182, SUP2Article

Inhibition of acetylcholinesterase by neurotoxic aminonitrilesFROINES, J. R.Biochemical pharmacology. 1985, Vol 34, Num 17, pp 3185-3187, issn 0006-2952Article

Divinylglykole zur Synthese von Desoxyhexosen ― Synthese von D- und L-Chalcose = Divinyl glycols pour la synthèse de désoxy hexoses: synthèse des D- et L-chalcose = Divinylglycols for the synthesis of deoxyhexoses: synthesis of D- and L-chalcoseKÜFNER, U; SCHMIDT, R. R.Angewandte Chemie. 1986, Vol 98, Num 1, pp 90-91, issn 0044-8249Article

Ingredient Profile: 2,3-Octanedione: Use in dairy, cooked vegetable and fruit profilesLIPKA, Cyndie; GREENLEAF, Sethness.Perfumer & flavorist. 2011, Vol 36, Num 7, issn 0272-2666, p. 22Article

Les cétones grasses: une nouvelle classe de composés lipochimiques de base? = Fatty ketones. A new class of building blocks for lipochemical compounds ?PIOCH, D; GRAILLE, J.OCL. Oléagineux, corps gras, lipides. 1994, Vol 1, Num 2, pp 94-95, issn 1258-8210Article

A new transitory product in the ozonolysis of trans-2-butene at atmospheric pressureHORIE, O; MOORTGAT, G. K.Chemical physics letters. 1989, Vol 156, Num 1, pp 39-46, issn 0009-2614Article

Die kinetik der reaktion von 2-propylchlorformiat mit alkalirhodaniden. II: Der reaktionsweg zur bildung des 2-Propoxycarbonylisothiocyanats = La cinétique de la réaction du chloroformiate de propyle-2 avec des sulfocyanures alcalins. II: Mécanisme de réaction de la formation des propoxy-2carbonyl isothiocyanates = Kinetic reaction of 2-propylchloroformiate with alkalin sulfocyanides. II: Reaction mechanism of formation 2-propoxycarbonyl isothiocyanatesDRAGALOV, V. V; LAVROV, V. E.Phosphorus and sulfur and the related elements. 1988, Vol 39, Num 3-4, pp 257-260, issn 0308-664XArticle