Nitroalkenes as precursors to the aromatic spiroketal skeleton of γ-rubromycin. A Nef-type reaction mediated by Pearlman's catalyst
暂无分享,去创建一个
[1] R. Varma,et al. Microwave-assisted Henry reaction: Solventless synthesis of conjugated nitroalkenes , 1997 .
[2] B. Goldstein,et al. Semisynthetic derivatives of purpuromycin as potential topical agents for vaginal infections. , 1997, Journal of medicinal chemistry.
[3] K. Nishikawa,et al. Heliquinomycin, a new inhibitor of DNA helicase, produced by Streptomyces sp. MJ929-SF2 II. Structure determination of heliquinomycin. , 1997, The Journal of antibiotics.
[4] R. Ballini,et al. Nitroaldol Reaction in Aqueous Media: An Important Improvement of the Henry Reaction. , 1997, The Journal of organic chemistry.
[5] K. Nishikawa,et al. Heliquinomycin, a new inhibitor of DNA helicase, produced by Streptomyces sp. MJ929-SF2 I. Taxonomy, production, isolation, physico-chemical properties and biological activities. , 1996, The Journal of antibiotics.
[6] J. Vora,et al. Synthesis, Chemical Transformation and Antimicrobial Activity of a Novel Class of Nitroolefins: 1,3-Diaryl-2-nitroprop-1-enes , 1994 .
[7] H. W. Pinnick. The Nef Reaction , 1990 .
[8] W. Schleif,et al. Inhibition of human immunodeficiency virus-1 reverse transcriptase activity by rubromycins: competitive interaction at the template.primer site. , 1990, Molecular pharmacology.
[9] R. Ballini,et al. New and efficient synthesis of ω-nitroalcohols and spiroketals by chemio- and regioselective reductive cleavage of 2-nitrocycloalkanones , 1990 .
[10] R. Ballini,et al. Functionalized Nitroalkanes in Synthesis of 1,6-Dioxaspiro[4.5]decane Components of Paravespula vulgaris Pheromone , 1989 .
[11] R. Ballini,et al. Nitromethane as d1,d1 Multiple Coupling Reagent for the Carbonyl Dianion Synthon. Practical Synthesis of Chalcogran , 1986 .
[12] R. Varma,et al. The Palladium Assisted Transfer Reduction of α, β-Unsaturated Nitroalkenes Using Sodium Hypophosphite: A Synthesis of Oximes , 1986 .
[13] R. Varma,et al. Selective Reduction of a, β-Unsaturated Nitrocompounds with Sodium Borohydride in Methanolic Solutions: A Facile Route to Nitroalkenes , 1985 .
[14] A. Deana,et al. Utilization of the chiral synthon, methyl 3-O-benzyl-2,4,6-trideoxy-6-iodo-α-D-erythro-hexopyranoside in the synthesis of a potent HMG-CoA reductase inhibitor , 1985 .
[15] Y. Takéuchi,et al. Pyranonaphthoquinone antibiotics. 4. Total synthesis of (+)-griseusin A, an enantiomer of the naturally occurring griseusin A , 1983 .
[16] P. Gramatica,et al. Reaction of nitroolefins with raney nickel and sodium hypophosphite. A mild method for converting nitroolefins into ketones (or aldehydes). , 1983 .
[17] P. Roller,et al. Isolation and structure elucidation of a novel griseorhodin. , 1979, The Journal of antibiotics.
[18] K. Eckardt,et al. The structure of the antibiotic griseorhodin C. , 1978, The Journal of antibiotics.
[19] G. Lancini,et al. Purpuromycin, a new antibiotic isolated from Actinoplanes ianthinogenes N. sp. , 1974, The Journal of antibiotics.
[20] C. Coronelli,et al. Structure determination of purpuromycin, a new antibiotic , 1974 .
[21] A. Zeeck,et al. Rubromycine, III. Die Konstitution von α‐Rubromycin, β‐Rubromycin, γ‐Rubromycin und γ‐iso‐Rubromycin , 1970 .