Unexpected tandem ylide annulation reaction for controllable synthesis of 2H-chromenes and 4H-chromenes.
暂无分享,去创建一个
Yong Tang | L. Ye | Xiu-Li Sun | Chunyin Zhu
[1] Yundong Wu,et al. Enantioselective synthesis of vinylcyclopropanes and vinylepoxides mediated by camphor-derived sulfur ylides: rationale of enantioselectivity, scope, and limitation. , 2006, Journal of the American Chemical Society.
[2] W. V. Otterlo,et al. Ring-closing metathesis for the synthesis of 2H- and 4H-chromenes , 2005 .
[3] J. Berger,et al. (2R)-2-methylchromane-2-carboxylic acids: discovery of selective PPARalpha agonists as hypolipidemic agents. , 2005, Bioorganic & medicinal chemistry letters.
[4] H. Wilkinson,et al. Estrogen receptor ligands. Part 10: Chromanes: old scaffolds for new SERAMs. , 2005, Bioorganic & medicinal chemistry letters.
[5] S. Bräse,et al. Base‐Catalyzed Condensation of 2‐Hydroxybenzaldehydes with α,β‐Unsaturated Aldehydes – Scope and Limitations , 2005 .
[6] H. Lebel,et al. Multicatalytic processes using diverse transition metals for the synthesis of alkenes. , 2004, Journal of the American Chemical Society.
[7] M. Mor,et al. Synthesis, pharmacological evaluation, and structure-activity relationships of benzopyran derivatives with potent SERM activity. , 2004, Bioorganic & medicinal chemistry.
[8] Margaret S. Wu,et al. (2R)-2-Ethylchromane-2-carboxylic Acids: Discovery of Novel PPARα/γ Dual Agonists as Antihyperglycemic and Hypolipidemic Agents , 2004 .
[9] Han-Dong Sun,et al. New isoprenylated flavones, artochamins A--E, and cytotoxic principles from Artocarpus chama. , 2004, Journal of natural products.
[10] M. Itoigawa,et al. Isoflavonoids from Dalbergia olivari. , 2003, Phytochemistry.
[11] S. Phongpaichit,et al. Antibacterial xanthones from the leaves of Garcinia nigrolineata. , 2003, Journal of natural products.
[12] Yuguo Du,et al. Total synthesis of the highly potent anti-HIV natural product daurichromenic acid along with its two chromane derivatives, rhododaurichromanic acids A and B. , 2003, Organic letters.
[13] J. Mbanya,et al. Griffonianone D, an isoflavone with anti-inflammatory activity from the root bark of Millettia griffoniana. , 2003, Journal of natural products.
[14] H. Schoemaker,et al. Ring-closing metathesis of allylic O,O- and N,O-acetals. , 2002 .
[15] K. Marquis,et al. New generation dopaminergic agents. Part 8: heterocyclic bioisosteres that exploit the 7-OH-2-(aminomethyl)chroman D(2) template. , 2002, Bioorganic & medicinal chemistry letters.
[16] A. Henriques,et al. Two chromene derivatives from Calyptranthes tricona. , 2000, Phytochemistry.
[17] C. Melchiorre,et al. Structure-activity relationships in 1,4-benzodioxan-related compounds. 6. Role of the dioxane unit on selectivity for alpha(1)-adrenoreceptor subtypes. , 1999, Journal of medicinal chemistry.
[18] H. Yamashita,et al. Synthesis and pharmacological characterization of novel 6-fluorochroman derivatives as potential 5-HT1A receptor antagonists. , 1998, Journal of medicinal chemistry.
[19] E. Ciganek. Esters of 2,3-Dihydro-3-oxobenzofuran-2-acetic Acid and 3,4-Dihydro-4-oxo-2H-1-benzopyran-3-acetic Acid by Intramolecular Stetter Reactions , 1995 .
[20] R. Tabacchi,et al. Two volatile β-chromenes fromWisteria sinensis flowers , 1994 .
[21] W. Kirmse,et al. Intramolecular addition reactions of functionalized arylcarbenes to double bonds , 1991 .
[22] U. Jacobsson,et al. Synthesis and characterization of all four isomers of methyl 2,4-decadienoate for an investigation of the pheromone components of Pityogenes chaicographus , 1988 .
[23] K. Mori,et al. Synthesis and biological activity of optically active forms of (E)-3, 7-dimethyl-2-octene-1, 8-dioic acid (callosobruchusic acid) , 1983 .