Chirale Cyclobutanone durch [2+2]-Cycloaddition von Dichlorketen an Kohlenhydratenolether = Chiral cyclobutanones by [2+2] cycloaddition of dichloroketene to carbohydrate enol ethersREDLICH, H; LENFERS, J. B; KOPF, J et al.Angewandte Chemie. 1989, Vol 101, Num 6, pp 764-765, issn 0044-8249, 2 p.Article

Bismuth trichloride as a new efficient catalyst in the aldol reactionOHKI, H; WADA, M; AKIBA, K.-Y et al.Tetrahedron letters. 1988, Vol 29, Num 37, pp 4719-4722, issn 0040-4039Article

Rate enhancement in the wacker oxidation of hydroxy-α,β-unsaturated esters : a fast neutral method for the preparation of masked β-ketoestersAUCLAIR, S. X; MORRIS, M; STURGESS, M. A et al.Tetrahedron letters. 1992, Vol 33, Num 50, pp 7739-7742, issn 0040-4039Article

A novel and unusual reaction of enol ethers with benzyltriethylammonium borohydride and chlorotrimethylsilaneBASKARAN, S; CHIDAMBARAM, N; NARASIMHAN, N et al.Tetrahedron letters. 1992, Vol 33, Num 42, pp 6371-6374, issn 0040-4039Article

Acylsilane chemistry. Synthesis of regio- and stereoisomerically defined enol silyl ethers using acylsilanesREICH, H. J; HOLTAN, R. C; BOLM, C et al.Journal of the American Chemical Society. 1990, Vol 112, Num 14, pp 5609-5617, issn 0002-7863Article

Synthesis of β-methoxy enones via a new two-carbon extension of carboxylic acidsHUDLICKY, T; OLIVO, H. F; NATCHUS, M. G et al.Journal of organic chemistry. 1990, Vol 55, Num 15, pp 4767-4770, issn 0022-3263, 4 p.Article

Acyclic tertiary and quaternary carbon stereocontrol via new aldol equivalent reactions of optically active (E)-enol ethersFAUNCE, J. A; FRIEBE, T. L; GRISSO, B. A et al.Journal of the American Chemical Society. 1989, Vol 111, Num 12, pp 4508-4510, issn 0002-7863Article

Water-promoted organic reactions: aldol reaction under neutral conditionsLUBINEAU, A.Journal of organic chemistry. 1986, Vol 51, Num 11, pp 2142-2144, issn 0022-3263Article

Unusual allylic acetoxylations of silyl enol ethers with lead(IV) acetateCRILLEY, M. M. L; LARSEN, D. S; STOODLEY, R. J et al.Tetrahedron letters. 1993, Vol 34, Num 20, pp 3305-3308, issn 0040-4039Article

New trialkylsilyl enol ether chemistry. Conjugate additions without the enoneMAGNUS, P; LACOUR, J.Journal of the American Chemical Society. 1992, Vol 114, Num 10, pp 3993-3994, issn 0002-7863Article

Pyridine-derived triflating reagents : an improved preparation of vinyl triflates from metallo enolatesCOMINS, D. L; ALI DEHGHANI.Tetrahedron letters. 1992, Vol 33, Num 42, pp 6299-6302, issn 0040-4039Article

A convenient synthesis of alkyl 2-nitrovinyl ethers. Conjugate addition of an alkoxide to give a nitroacetaldehyde mixed acetalKOGAN, T. P; GAETA, F. C. A.Synthesis (Stuttgart). 1988, Num 9, pp 706-707, issn 0039-7881Article

Asymmetric aldol reaction of silyl enol ethers with aldehydes promoted by the combined use of chiral diamine coordinated tin(II) triflate and tributyltin fluorideKOBAYASHI, S; MUKAIYAMA, T.Chemistry Letters. 1989, Num 2, pp 297-300, issn 0366-7022, 4 p.Article

Further studies on the mutagenic activity of fecapentaene-12 analogues and conclusions about their molecular mode of actionVERTEGAAL, L. B. J; VOODG, C. E; MOHN, G. R et al.Mutation research. Mutation research letters. 1992, Vol 281, Num 2, pp 93-98, issn 0165-7992Article

Dimethyldioxirane epoxidation of β-oxo enol ethersADAM, W; HADJIARAPOGLOU, L.Chemische Berichte. 1990, Vol 123, Num 10, pp 2077-2079, issn 0009-2940Article

Facile preparation of α-nitroketones from enol silyl ethersRAJENDRA RATHORE; ZHE LIN; KOCHI, J. K et al.Tetrahedron letters. 1993, Vol 34, Num 12, pp 1859-1862, issn 0040-4039Article

Plasmalogenepoxide als biologische Vorstufen von α-Hydroxyaldehyden = Plasmalogen epoxides as biological precursors of α-hydroxyaldehydesDUDDA, A; SPITELLER, G.Liebigs Annalen der Chemie. 1993, Num 12, pp 1249-1251, issn 0170-2041Article

Divergent stereoselective synthesis of (E) and (Z) O-alkyl enol ethersSOLA, L; CASTRO, J; MOYANO, A et al.Tetrahedron letters. 1992, Vol 33, Num 20, pp 2863-2866, issn 0040-4039Article

Alternatives to α-diazo ketones for tandem cyclization-cycloaddition and carbenoid-alkyne metathesis strategies. Novel cyclic enol-ether formation via carbonyl ylide rearrangement reactionsFAIRFAX, D. J; AUSTIN, D. J; XU, S. L et al.Journal of the Chemical Society. Perkin transactions. I. 1992, Num 21, pp 2837-2844, issn 0300-922XArticle

Ethoxymethylenemalonates and malononitriles (EMM reagents) as formic acid equivalents : synthesis of fused-imidazoles under neutral or mildly acidic conditionsSEGELSTEIN, B. E; CHENARD, B. L; MACOR, J. E et al.Tetrahedron letters. 1993, Vol 34, Num 12, pp 1897-1900, issn 0040-4039Article

Vinyl ether hydrolysis. XXVIII: The mechanism of reaction of methyl α-(2,6-dimethoxyphenyl)vinyl etherJONES, J; KRESGE, A. J.Canadian journal of chemistry (Print). 1993, Vol 71, Num 1, pp 38-41, issn 0008-4042Article

The stereoselective hydrogenation of nepetalactoles: the role of C1 alkoxyl groups on the stereoselectivityKIGAWA, M; TANAKA, M; KATSUHARA, T et al.Heterocycles (Sendai). 1993, Vol 35, Num 2, pp 615-618, issn 0385-5414Article

A novel electrophilic methoxylation (with a little help from F₂)ROZEN, S; MISHANI, E; KOL, M et al.Journal of the American Chemical Society. 1992, Vol 114, Num 20, pp 7643-7645, issn 0002-7863Article

Enols deriveed from malonic acids as intermediates in nitrosation and halogenationWILLAMS, D. L. H; GRAHAM, A.Tetrahedron (Oxford. Print). 1992, Vol 48, Num 37, pp 7973-7978, issn 0040-4020Article

Acyclic stereocontrol in Michael addition reactions of enamines and enol ethersOARE, D. A; HEATHCOCK, C. H.Topics in stereochemistry. 1991, Vol 20, pp 87-170, issn 0082-500X, 84 p.Article