1,2-Asymmetric induction on conjugate addition to chiral γ-substituted-α,β-unsaturated aldehydeHONDA, Y; HIRAI, S; TSUCHIHASHI, G et al.Chemistry Letters. 1989, Num 2, pp 255-258, issn 0366-7022, 4 p.Article

A new vinylic organolithium reagent : an expedient C₁₀+C₁₀ synthesis of retinalDUHAMEL, L; DUHAMEL, P; LE GALLIC, Y et al.Tetrahedron letters. 1993, Vol 34, Num 2, pp 319-322, issn 0040-4039Article

Cleavage and oligomerization of malondialdehyde under physiological conditionsGOMEZ-SANCHEZ, A; HERMOSIN, I; MAYA, I et al.Tetrahedron letters. 1990, Vol 31, Num 28, pp 4077-4080, issn 0040-4039, 4 p.Article

Synthèse des aldehydes para-hydroxycinnamiques substrats de l'alcool cinnamylique deshydrogénase = Synthesis of para-hydroxycinnamaldehyde substrates of cinnamic alcohol dehydrogenaseDURAN, E; DURAN, H; GORRICHON, L et al.Holzforschung. 1992, Vol 46, Num 1, pp 21-24, issn 0018-3830Article

Flavor Bites: trans-2-DecenalWRIGHT, John.Perfumer & flavorist. 2010, Vol 35, Num 11, pp 34-35, issn 0272-2666, 2 p.Article

Pyrrole aus 3-alkoxyacroleinen und CH-aciden α-aminoessig-säure-derivaten = Pyrroles from 3-alcoxyacroleines and CH-acids derivatives of α-aminoacetic acidsHASSAN WALIZEI, G; BREITMAIER, E.Synthesis (Stuttgart). 1989, Num 4, pp 337-340, issn 0039-7881, 4 p.Article

An artificial visual pigment with restricted C₉-C₁₁ motion forms normal photolysis intermediatesSHEVES, M; ALBECK, A; OTTOLENGHI, M et al.Journal of the American Chemical Society. 1986, Vol 108, Num 20, pp 6440-6441, issn 0002-7863Article

[¹⁴]C acrolein accumulation and metabolism in leaf lettuceNORDONE, A. J; KOVACS, M. F; DOANE, R et al.Bulletin of environmental contamination and toxicology. 1997, Vol 58, Num 5, pp 787-792, issn 0007-4861Article

A new asymmetric route to bridged indole alkaloids : formal syntheses of (-)-suaveoline, (-)-raumacline and (-)-N^b-methylraumaclineBAILEY, P. D; COLLIER, I. D; HOLLINSHEAD, S. P et al.Journal of the Chemical Society. Chemical communications. 1994, Num 13, pp 1559-1560, issn 0022-4936Article

Kinetische Untersuchung zur Hydratisierung von Acrolein = Kinetic studies on the hydration of acroleinARNTZ, D; HAAS, T; MUÊLLER, A et al.Chemieingenieurtechnik. 1991, Vol 63, Num 7, pp 733-735, issn 0009-286X, 3 p.Article

Amélioration du procédé de préparation de l'aldéhyde cinnamiqueANDREEVA, L. K; KHEJFITS, L. A; SAMOKHVALOVA, N. G et al.Maslo-žirovaâ promyšlennost'. 1986, Num 11, pp 27-28, issn 0025-4649Article

Conversion of (+)-carotol into (-)-carota-1,4-dienaldehydeHASHIDOKO, Y; TAHARA, S; MIZUTANI, J et al.Bioscience, biotechnology, and biochemistry. 1992, Vol 56, Num 11, pp 1892-1893, issn 0916-8451Article

A very short, highly efficient synthesis of natural (-)-warburganalNAKANO, T; MARTIN, A.Journal of chemical research. Synopses (Print). 1989, Num 2, pp 52-53, issn 0308-2342Article

Crucial parameters in the selective biphasic hydrogenation of cinnamaldehyde by biphasic Ru-TPPTS and RhCl(TPPTS)₃ catalystsNUITHITIKUL, Kamchai; WINTERBOTTOM, Mike.Catalysis today. 2007, Vol 128, Num 1-2, pp 74-79, issn 0920-5861, 6 p.Article

New rearrangement of 4-isoxazoline system: Conversion of ketones into α, β-unsaturated amidesCHIACCHIO, Ugo; RESCIFINA, Antonio; CHIACCHIO, Maria Assunta et al.Journal of organic chemistry. 2003, Vol 68, Num 9, pp 3718-3720, issn 0022-3263, 3 p.Article

Cycloaddition of chlorosulfonyl isocyanate with arylmethylenemalonaldehydesDANIEL, J; DURGA NATH DHAR.Tetrahedron (Oxford. Print). 1992, Vol 48, Num 22, pp 4551-4554, issn 0040-4020Article

The genetic toxicology of cinnamaldehydeNEUDECKER, T.Mutation research. Reviews in genetic toxicology. 1992, Vol 277, Num 3, pp 173-185, issn 0165-1110Article

Catalytic conversion of glycerol to value added liquid productsPATHAK, Kapil; MOHAN REDDY, K; BAKHSHI, N. N et al.Applied catalysis. A, General (Print). 2010, Vol 372, Num 2, pp 224-238, issn 0926-860X, 15 p.Article

Ultrasound-assisted hydrogenation of cinnamaldehydeDISSELKAMP, R. S; HART, T. R; WILLIAMS, A. M et al.Ultrasonics sonochemistry. 2005, Vol 12, Num 4, pp 319-324, issn 1350-4177, 6 p.Article

La reaction de Diels-Alder sous irradiation micro-onde avec le graphite comme support = Diels-Alder reaction under microwave irradiation with graphite as supportLAPORTE, C; OUSSAID, A; GARRIGUES, B et al.Comptes rendus de l'académie des sciences. Serie IIc, chimie. 2000, Vol 3, Num 4, pp 321-325, issn 1387-1609Article

The Vilsmeier reaction on dithioketals : a facile method for the stereoselective synthesis of β-alkylthioethylenic aldehydesASOKAN, C. V; MATHEWS, A.Tetrahedron letters. 1994, Vol 35, Num 16, issn 0040-4039, 2448, 2585-2586 [3 p.]Article

Aminoborohydrides. II: Regiospecific reductions of α,β-unsaturated carbonyl compounds with lithium pyrrolidinoborhydride. A facile conversion of α,β-unsaturated aldehydes and ketones to the corresponding allylic alcohols in high purityFULLER, J. C; STANGELAND, E. L; GORALSKI, C. T et al.Tetrahedron letters. 1993, Vol 34, Num 2, pp 257-260, issn 0040-4039Article

Tin(II) chloride dihydrate : a mild and efficient reagent for cleaving acetalsFORD, K. L; ROSKAMP, E. J.Tetrahedron letters. 1992, Vol 33, Num 9, pp 1135-1138, issn 0040-4039Article

A simple synthesis of α-acaridialSUZUKI, T; MATSUYAMA, S; KUWAHARA, Y et al.Bioscience, biotechnology, and biochemistry. 1992, Vol 56, Num 11, pp 1888-1889, issn 0916-8451Article

Alkylation of carbonyl compounds with dialkylzirconocene complexes promoted by potassium t-butoxideLARSON, A. L; BAKER, D. L; TOWNE, R. W et al.Tetrahedron letters. 1991, Vol 32, Num 42, pp 5893-5894, issn 0040-4039Article