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排序方式: 共有137条查询结果,搜索用时 46 毫秒
31.
Alexander J Artuso M Bebek C Berkelman K Browder T Cassel DG Cheu E Coffman DM Crawford G DeWire JW Drell PS Ehrlich R Galik RS Gittelman B Gray SW Halling AM Hartill DL Heltsley BK Kandaswamy J Katayama N Kreinick DL Lewis JD Ludwig GS Mistry NB Mueller J Nandi S Nordberg E O'Grady C Peterson D Pisharody M Riley D Sapper M Selen M Silverman A Stone S Worden H Worris M Sadoff AJ Avery P Besson D Garren L Yelton J Bowcock T Kinoshita K Pipkin FM Procario M Wilson R Wolinski J Xiao D Zhu Y 《Physical review letters》1990,65(13):1531-1534
32.
Sabir H Mashraqui Mamta B Patil Yogesh Sangvikar Mohamed Ashraf Hitesh D Mistry Elise Trn Huu Dub Auke Meetsma 《Journal of heterocyclic chemistry》2005,42(5):947-954
Synthesis of biaryl type systems, 11‐aryl/heteroarylnaphtho[2,1‐b]furans 8‐11 has been described with a view to studying the conformational orientation of C‐11 aryl/heteroaryl groups. Synthesis of 8‐11 was accomplished by a two‐step sequence involving O‐alkylation of 2‐naphthol with appropriate halo‐ketones 2‐4 , followed by cyclization of the resulting naphthoxy‐ketones 5‐7 with methanesulphonic acid. The structures of 8‐11 are based on detailed 2D NMR spectral analysis. The H8 in these compounds is not subject to significant anisotropic upfield shielding effects. The slightly upfield chemical shift of H8 in molecules 9‐11 , relative to 8 has been correlated with the electron density at C17 and C8 positions. While molecular modeling indicated dihedral angle (φ) between the C11 aryl/heteroaryl groups and the naphthofuran plane to be in the range of 70–60° in 8‐10 , a single X‐ray crystal structural analysis of 11‐(4′‐pyridyl)naphtho[2,1‐b]furan 10 indicated (φ) of 64.36°. In view of significant deviations from the orthogonal oreintation, the absence of any significant anisotropic shielding in 8‐11 is not entirely unexpected. 相似文献
33.
Alam MS Katayama N Kim IJ Li WC Lou XC Sun CR Bortoletto D Goldberg M Horwitz N Mestayer MD Moneti GC Sharma V Shipsey IP Skwarnicki T Csorna SE Letson T Brock IC Ferguson T Artuso M Bebek C Berkelman K Blucher E Byrd J Cassel DG Cheu E Coffman DM Crawford G DeSalvo R DeWire JW Drell PS Ehrlich R Galik RS Gittelman B Gray SW Halling AM Hartill DL Heltsley BK Kandaswamy J Kowalewski R Kreinick DL Kubota Y Lewis JD Mistry NB Mueller J Namjoshi R Nandi S Nordberg E O'Grady C Peterson D Pisharody M 《Physical review D: Particles and fields》1989,40(3):712-720
34.
Csorna SE Mestayer MD Panvini RS Word GB Yi X Bean A Bobbink GJ Brock I Engler A Ferguson T Kraemer R Rippich C Sutton R Vogel H Bebek C Berkelman K Blucher E Cassel DG Copie T DeSalvo R DeWire JW Ehrlich R Galik RS Gilchriese MG Gittelman B Gray SW Halling AM Hartill DL Heltsley BK Holzner S Ito M Kandaswamy J Kowalewski R Kreinick DL Kubota Y Mistry NB Mueller J Nordberg E Ogg M Peterson D Perticone D Pisharody M Read K Riley D Silverman A Stein PC Stone S Sadoff AJ Avery P Besson D Bowcock T 《Physical review letters》1986,56(12):1222-1225
35.
Bebek C Berkelman K Blucher E Cassel DG Copie T DeSalvo R DeWire JW Ehrlich R Galik RS Gilchriese MG Gittelman B Gray SW Halling AM Hartill DL Heltsley BK Holzner S Ito M Kandaswamy J Kowalewski R Kreinick DL Kubota Y Mistry NB Mueller J Nordberg E Ogg M Peterson D Perticone D Pisharody M Read K Riley D Silverman A Stein PC Stone S Sadoff AJ Avery P Besson D Bowcock T Giles RT Hassard J Kinoshita K Pipkin FM Wilson R Haas P Hempstead M Jensen T Kagan H Kass R Behrends S Gentile T Guida JM 《Physical review letters》1986,56(18):1893-1896
36.
Bean A Bobbink GJ Brock IC Engler A Ferguson T Kraemer RW Rippich C Vogel H Bebek C Berkelman K Blucher E Cassel DG Copie T DeSalvo R DeWire JW Ehrlich R Galik RS Gilchriese MG Gittelman B Gray SW Halling AM Hartill DL Heltsley BK Holzner S Ito M Kandaswamy J Kowalewski R Kreinick DL Kubota Y Mistry NB Mueller J Namjoshi R Nordberg E Ogg M Perticone D Peterson D Pisharody M Read K Riley D Silverman A Stone S Yi X Sadoff AJ Avery P Besson D Bowcock T Giles RT Hassard J Kinoshita K Pipkin FM 《Physical review letters》1987,58(3):183-186
37.
Csorna SE Garren L Mestayer MD Panvini RS Yi X Alam MS Avery P Bebek C Berkelman K Cassel DG Copie T DeSalvo R DeWire JW Ehrlich R Ferguson T Galik R Gilchriese MG Gittelman B Halling M Hartill DL Holzner S Ito M Kadaswamy J Kreinick DL Kubota Y Mistry NB Nordberg E Ogg M Peterson D Perticone D Read K Silverman A Stein PC Stone S Kezun X Sadoff AJ Giles RT Hassard J Hempstead M Kinoshita K McKay WW Pipkin FM Wilson R Haas P Jensen T Kagan H Kass R Behrends S Gentile T Guida JM Guida JA Morrow F 《Physical review letters》1985,54(17):1894-1897
38.
39.
Ravindra D. Jadhav Hitesh D. Mistry Hashim Motiwala Kishorkumar S. Kadam Shivaji Kandre Amol Gupte Ashok K. Gangopadhyay Rajiv Sharma 《Journal of heterocyclic chemistry》2013,50(4):774-780
Hydroxy (tosyloxy) iodobenzene (HTIB), a hypervalent iodine reagent, has been extensively used for oxidative transformations. We have developed a one‐pot synthesis wherein aldoximes when reacted with alkynes in the presence of HTIB result in the direct formation of isoxazoles. This simple and straightforward reaction allows for ease of purification while leading to the formation of high purity 3,5‐disubstituted isoxazoles in moderate yields. 相似文献
40.