An antibody-catalyzed oxy-cope rearrangementBRAISTED, A. C; SCHULTZ, P. G.Journal of the American Chemical Society. 1994, Vol 116, Num 5, pp 2211-2212, issn 0002-7863Article

Simplification of the cope loop catheterROLL, J. D; CASTANEDA-ZUNIGA, W. R; HUNTER, D. W et al.Seminars in interventional radiology. 1987, Vol 4, Num 1, issn 0739-9529, 46Article

Supramolecular catalysis of unimolecular rearrangements : Substrate scope and mechanistic insightsFIEDLER, Dorothea; VAN HALBEEK, Herman; BERGMAN, Robert G et al.Journal of the American Chemical Society. 2006, Vol 128, Num 31, pp 10240-10252, issn 0002-7863, 13 p.Article

Tris-aza-cope rearrangement of bicyclic N-cyano-N'-vinyl or N'-arylhydrazines to imidazolo-diazepine derivativesROUSSELLE, D; MUSICK, C; VIEHE, H. G et al.Tetrahedron letters. 1991, Vol 32, Num 7, pp 907-910, issn 0040-4039, 4 p.Article

Cope rearrangement of 3,3-dicyanohexa-1,5-dieneDEWAR, M. J. S; CAOXIAN JIE.Journal of the Chemical Society. Chemical communications. 1989, Num 2, pp 98-100, issn 0022-4936, 3 p.Article

3,7-Dicyan-2,6-dimethoxy-1,5-dimethylsemibullvalen = Dicyano-3,7 dimèthoxy-2,6 diméthyl-1,5 semibulvalène = 3,7-Dicyano-2,6 dimethoxy-1,5 dimethylsemibullvaleneQUAST, H; KLAUBERT, C. A; JACKMAN, L. M et al.Chemische Berichte. 1988, Vol 121, Num 10, pp 1801-1806, issn 0009-2940Article

Synthetic photochemistry. XLVII: Formation and degenerate cope rearrangement of 9-dicyanomethylenebarbaralaneGUAN RONG TIAN; SUGIYAMA, S; MORI, A et al.Bulletin of the Chemical Society of Japan. 1989, Vol 62, Num 2, pp 614-615, issn 0009-2673, 2 p.Article

The development of a facile tandem wolff/cope rearrangement for the synthesis of fused carbocyclic skeletonsSARPONG, Richmond; SU, Julius T; STOLTZ, Brian M et al.Journal of the American Chemical Society. 2003, Vol 125, Num 45, pp 13624-13625, issn 0002-7863, 2 p.Article

Relevance of oxyanion stereochemistry to chirality transfer in anionic oxy-cope rearrangementsPAQUETTE, L. A; MAYNARD, G. D.Journal of the American Chemical Society. 1992, Vol 114, Num 13, pp 5018-5027, issn 0002-7863Article

Interconversion of the tetracyclo[6.3.0.0^4,11.0^5,9]undeca-2,6-diene and tetracyclo [7.2.0.0^4,11.0^6,10]undeca-2,7-diene ring systemsEATON, P. E; YU CHI YIP.Synlett. 1993, Num 1, pp 73-74, issn 0936-5214Article

Analysis of solvent effects on the rate of the cope rearrangement : evidence for its hydrogen-bond-insusceptible natureMITSUHASHI, T; YAMAMOTO, G.Bulletin of the Chemical Society of Japan. 1990, Vol 63, Num 2, pp 643-645, issn 0009-2673, 3 p.Article

Ring-opening metathesis/oxy-cope rearrangement: A new strategy for the synthesis of bicyclic medium ring-containing compoundsWHITE, Brian H; SNAPPER, Marc L.Journal of the American Chemical Society. 2003, Vol 125, Num 48, pp 14901-14904, issn 0002-7863, 4 p.Article

Chiral synthesis of novel α-yohimbane alkaloids (-)-nitraraine and (-)-dihydronitraraineTAKANO, S; SAMIZU, K; SUGIHARA, T et al.Chemistry Letters. 1989, Num 10, pp 1777-1780, issn 0366-7022Article

Diastereoselective Construction of Quaternary Carbons Directed via Macrocyclic Ring Conformation : Formal Synthesis of (-)-MesembrineAMS, Steve; LEBRUN, Marie-Eve; GRISE, Christiane M et al.Journal of organic chemistry. 2007, Vol 72, Num 24, pp 9314-9322, issn 0022-3263, 9 p.Article

Thermolabile Kohlenwasserstoffe. XXXII: Konkurrierende Cope-Umlagerung und Homolyse von meso- und DL-3,4-Di(1-cyclohexen-1-yl)-2,2,5,5-tetramethylhexan = Thermolabile hydrocarbons. XXXII: Competing Cope rearrangement and homolytic decomposition of meso- and DL-3,4-di(1-cyclohexen-1-yl)-2,2,5,5-tetramethylhexaneHERBERG, C; BECKHAUS, H.-D; KÖRTVELYESI, T et al.Chemische Berichte. 1993, Vol 126, Num 1, pp 117-127, issn 0009-2940Article

Synthetic utility of amine N-oxidesALBINI, A.Synthesis (Stuttgart). 1993, Num 3, pp 263-277, issn 0039-7881Article

A stereoconvergent approach to dicyclopenta[a,d]cyclooctane terpenoids via a very mild Cope reactionJOMMI, G; ORSINO, F; RESMINI, M et al.Tetrahedron letters. 1991, Vol 32, Num 47, pp 6969-6972, issn 0040-4039Article

Anwendungen der ¹³C-NMR-Spektroskopie. XXVIII: Die Aktivierungsparameter der Cope-Umlagerung von 3,7-Diethoxy-1,5-dimethyl-2,4,6,8-tetraazabarbaralan = Application de la spectroscopie RMN-¹³C. XXVIII: Paramètres d'activation de la transposition de Cope du diméthyl-1,5 diéthoxy-3,7 tétraaza-2,4,6,8-barbaralane = Application of ¹³C-NMR spectroscopy. XXVIII: Activation parameters of the Cope rearrangement of 1,5-dimethyl 3,7-diethoxy 2,4,6,8-tetraazabarbaralaneMOSKAU, D; LEBER, W; GÜNTHER, H et al.Chemische Berichte. 1989, Vol 122, Num 12, pp 2361-2364, issn 0009-2940Article

Facile [3,3] rearrangement of substituted 3α- -5α-hydroxy-tricyclo[5.2.1.0^2,6]decadienesSURI, S. C; RODGERS, S. L; LAUDERDALE, W. J et al.Tetrahedron letters. 1988, Vol 29, Num 33, pp 4031-4034, issn 0040-4039Article

The pathways of the combined Cope rearrangement : molecular reorientation process in solid bullvalene : a deuterium 2D exchange NMR study on a single crystalMÜLLER, A; HAEBERLEN, U; ZIMMERMANN, H et al.Molecular physics (Print). 1994, Vol 81, Num 5, pp 1239-1258, issn 0026-8976Article

Isomerization of diydroazulenes to substituted azulenes : naked eye observation of a novel Cope-type rearrangementHAFNER, K; HARTUNG, J; SYREN, C et al.Tetrahedron (Oxford. Print). 1992, Vol 48, Num 23, pp 4879-4884, issn 0040-4020Article

Enol variants of the cope rearrangement of cis-2,3-divinyl epoxides and the further functionalization of the oxepin nucleusCHOU, W.-N; WHITE, J. B.Tetrahedron letters. 1991, Vol 32, Num 2, pp 157-160, issn 0040-4039, 4 p.Article

Synthesis and properties of 2,4,6-trimethylenetricyclo[3.3.0.0^3,7]octane (stellatriene) and its alkyl derivatives. Candidates for a two-step Cope rearrangementGLEITER, R; SIGWART, C.Journal of organic chemistry. 1994, Vol 59, Num 5, pp 1027-1038, issn 0022-3263Article

Effect of terminal fluorine substitution on the cope rearrangement : boat versus chair transition state. Evidence for a very significant fluorine steric effectDOLBIER, W. R; PALMER, K. W.Journal of the American Chemical Society. 1993, Vol 115, Num 20, pp 9349-9350, issn 0002-7863Article

Acyclic oxy-cope rearrangement : dependence of E/Z stereoselection on substrate stereochemistryTOMOOKA, K; SHIH-YI WEI; NAKAI, T et al.Chemistry Letters. 1991, Num 1, pp 43-46, issn 0366-7022, 4 p.Article