| ²é¿´: 435 | »Ø¸´: 1 | ||
772820536гæ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| CÆ×Êý¾Ý173.42,172.93,70.71,59.54,58.82,41.01,38.31,25.82,21.64,13.01,10.72;HÆ×Êý¾Ý3.97,3.85,2.29,1.95,1.60,1.50,1.38,0.97,0.92,0.89£¬Çë¸ø³öÏàËÆ¶È¸ßµÄ»¯ºÏÎ×îºÃÏàËÆ¶ÈÄÜ´óÓÚ80% |
» ²ÂÄãϲ»¶
²ÄÁÏר˶283Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
²ÄÁÏÓ뻯¹¤306·ÖÕÒµ÷¼Á
ÒѾÓÐ13È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ10È˻ظ´
085600£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
0817»¯Ñ§¹¤³ÌÓë¼¼ÊõÇóµ÷¼Á£¬Ò»Ö¾Ô¸Öк£Ñó319
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸±±¾©2£¬²ÄÁÏÓ뻯¹¤308Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁÏÓ뻯¹¤371Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁÏר˶322·Ö
ÒѾÓÐ11È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ8È˻ظ´
·çÐÐÕß007
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1309 (½²Ê¦)
- ½ð±Ò: 12672.8
- ºì»¨: 15
- Ìû×Ó: 1490
- ÔÚÏß: 299.5Сʱ
- ³æºÅ: 2542465
- ×¢²á: 2013-07-12
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
ÏàËÆ¶ÈûÓдóÓÚ80%µÄϱßÊÇÈ«²¿½á¹û ²éѯ½á¹û£º¹²²éµ½30¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 5a ÏàËÆ¶È:58.3% Tetrahedron Letters 2000 41 8293-8296 Asymmetric synthesis of C-6 substituted pipecolic acid derivatives Sylvie Carbonnel, Catherine Fayet, Jacques Gelas, Yves Troin Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Ethyl 2-piperidinobutanoate C11H21NO2 ÏàËÆ¶È:54.5% Molecules 2001 6 892-899 Captodative Formyl Enamines in a New Synthesis of Tertiary ¦Á-Amino Esters Alexandre Y. Rulev, Lyudmila I. Larina and Mikhail G. Voronkov Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (3R,5R)-Methyl 3,5-dihydroxydecanoate C11H22O4 ÏàËÆ¶È:54.5% Canadian Journal of Chemistry 2009 87 650-661 Chiral ¦Á-substituted allylboronates in a one-potthree-component asymmetric allylic alkylation/carbonyl allylation reaction sequence -Applications to the syntheses of (+)-(3R,5R)-3-hydroxy-5-decanolide and (-)-massoialactone Lisa Carosi and Dennis G. Hall Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . methyl (¡À)-2-oxo-1-(3-oxopropyl)cyclohexanecarboxylate C11H16O4 ÏàËÆ¶È:54.5% Journal of Heterocyclic Chemistry 2003 40 113-120 N-phenyl-substituted pyrrolidines,piperidines and azabicyclics by a tandem reduction-double reductive amination reaction Richard A. Bunce,Derrick M. Herron,Jason R. Lewis and Sharadsrikar V. Kotturi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ethyl 4,6-dimethyl-5,7-diphenyl-6-aza-spiro[2.5]octane-1-carboxylate C24H29NO2 ÏàËÆ¶È:54.5% Indian Journal of Chemistry Section B 2007 46B 818-822 4-Piperidone ¨C A synthon for spiro-heterocycles Padmavathi,V; Reddy,T V Ramana; Reddy,K Audisesha Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Compound 1 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry Letters 1998 8 2375-2380 Combinatorial chemistry of hydantoins Astrid Boeijen, John A. W. Kruijtzer, Rob M. J. Liskamp Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (R)-3-Methoxymethyl-2-methyleneoctamide C11H21NO2 ÏàËÆ¶È:54.5% Chinese Journal of Chemistry 2002 20 1291-1299 Synthesis of Optically Active ¦Â - Alkyl -¦Á- methylene - ¦Ä - butyro -lactones from Enantioselective Biotransformation of Nitriles, an Unusual Inversion of Enantioselectivity† Sheng-Min Zhao and Mei-Xiang Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (S)-3-Methoxymethyl-2-methylenecxtanoic acid C11H18O3 ÏàËÆ¶È:54.5% Chinese Journal of Chemistry 2002 20 1291-1299 Synthesis of Optically Active ¦Â - Alkyl -¦Á- methylene - ¦Ä - butyro -lactones from Enantioselective Biotransformation of Nitriles, an Unusual Inversion of Enantioselectivity† Sheng-Min Zhao and Mei-Xiang Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-[(1R,2S)-1-hydroxy-2-methylbutyl]-4-methylfuran-2(5H)-one C10H16O3 ÏàËÆ¶È:54.5% Tetrahedron 2003 59 3237-3251 Bioactive butenolides from Streptomyces antibioticus T¨¹ 99: absolute configurations and synthesis of analogs Gilles Grossmann, Marc Poncioni, Marc Bornand, Benoı̂t Jolivet, Markus Neuburger, Urs S¨¦quin Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-[(1R,2S)-1-hydroxy-2-methylbutyl]-4-methylfuran-2(5H)-one C10H16O3 ÏàËÆ¶È:54.5% Tetrahedron 2003 59 3237-3251 Bioactive butenolides from Streptomyces antibioticus T¨¹ 99: absolute configurations and synthesis of analogs Gilles Grossmann, Marc Poncioni, Marc Bornand, Benoı̂t Jolivet, Markus Neuburger, Urs S¨¦quin Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 60 ÏàËÆ¶È:54.5% Tetrahedron 1995 51 8835-8852 Synthesis of tricyclopentanoid sesquiterpenes via rearrangement routes: (¡À)-modhephene, (¡À)-epimodhephene and (¡À)-isocomene Lutz Fitjer, Marita Majewski, Honorato Monz¨®-Oltra Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . permetin A ÏàËÆ¶È:54.5% The Journal of Antibiotics 1985 38 1610-1613 ABSOLUTE CONFIGURATION OF THE ¦Â-HYDROXYL FATTY ACID CONSTITUENT OF PERMETIN A ASAO MURAI, YUSUKE AMINO, TOSHIHIKO ANDO Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ethyl 3-hydroxy-3-methylheptanoate ÏàËÆ¶È:54.5% Journal of Chemical Ecology 1996 22 2233-2249 Identification of sex pheromones from cowpea weevil,Callosobruchus maculatus, and related studies withC. analis (coleoptera: Bruchidae) Thomas W. Phillips, Joel K. Phillips, Francis X. Webster, Rong Tang and Wendell E. Burkholder Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 2-methyl-2,5-bornandiol ÏàËÆ¶È:54.5% Annals of Microbiology 2010 60 249-253 Chemical constitutes from endophytic Streptomyces sp. W5 isolated from Trewia nudiflora L. Guozhu Wei, Na Zhu, Ying Zeng, Yuemao Shen, Peiji Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 1-(tert-butyldimethylsilyloxy)-3,3-bis(methoxymethyl)hex-5-yne C16H32O3Si ÏàËÆ¶È:54.5% Tetrahedron 2013 69 7659-7669 Cyclopropanes in Nicholas reaction: formation of spiroketals with a five-membered and a seven- or an eight-membered ring Chisato Mukai, Takahiro Kojima, Takamasa Kawamura, Fuyuhiko Inagaki Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . tetrabutylammonium bis(sec-heptyl)phosphate ÏàËÆ¶È:54.5% Tetrahedron 2013 69 9947-9950 A convenient two-step synthesis of dialkylphosphate ionic liquids Justyna Kotlarska, Koen Binnemans, Wim Dehaen Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (R)-3-(((tert-butyldimethylsilyl)oxy)methyl)-3-methylpentan-1-ol C13H30O2Si ÏàËÆ¶È:54.5% Molecules 2014 19 2213-2225 Synthesis of ∆3-2-Hydroxybakuchiol Analogues and Their Growth Inhibitory Activity against Rat UMR106 Cells Qun Zhao, Qianqian Xu, Guangsheng Shan, Chao Dong, Hong Zhang and Xinsheng Lei Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . n-propyl-3-hydroxyoctanoate ÏàËÆ¶È:54.5% Applied Microbiology and Biotechnology 2013 97 211-222 Polyester hydrolytic and synthetic activity catalyzed by the medium-chain-length poly(3-hydroxyalkanoate)depolymerase from Streptomyces venezuelae SO1 Marta Santos, Joana Gangoiti, Helmut Keul, Martin Möller, Juan L. Serra, Mar¨ªa J. Llama Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 3-(1-Hydroxy-2-methylbutyl)-4-methyl-2(5H)-franone ÏàËÆ¶È:54.5% FEMS Microbiology Letters 1995 126 37-42 New butenolides from the photoconductivity screening of Streptomyces antibioticus (Waksman and Woodruff) Waksman and Henrici 1948 Dieter Braun, Niklaus Pauli, Urs Sequin and Hans Zähner Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . rac-N-methyl-5-hydroxydecanamide ÏàËÆ¶È:54.5% Flavour and Fragrance Journal 2007 22 531-539 Asymmetric synthesis of ¦Ä-lactones with lipase catalyst Yasutaka Shimotori, Kazuki Sekine and Tetsuo Miyakoshi Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Ethyl 3-Hydroxy-3-methylheptanoate ÏàËÆ¶È:54.5% Journal of Chemical Ecology 1996 22 2233-2249 Identification of sex pheromones from cowpea weevil,Callosobruchus maculatus, and related studies withC. analis (coleoptera: Bruchidae) Thomas W. Phillips, Joel K. Phillips, Francis X. Webster, Rong Tang, Wendell E. Burkholder Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ¦Á-{3-[2-hydroxy-3-(N-methyl-N-hydroxyethylcmino)propoxy]propyl}-w-butylpolydimethylsiloxane ÏàËÆ¶È:53.8% Chinese Chemical Letters 2008 19 1196-1198 Synthesis and characterization of ¦Á-{3-[2-hydroxy-3-(N-methyl-N-hydroxy-ethylamino)propoxy]propyl} -w-butylpolydimethylsiloxanes Hai Feng Sun, Qing Si Zhang , Meng Zhang , Yi Tao Yu, Jian Ping Zong Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . compound 1b ÏàËÆ¶È:53.8% Magnetic Resonance in Chemistry 1985 23 137-138 Carbon-13 NMR study of some new macrocycles. 13C chemical shifts of nactin antibiotic models M. El Malouli Bibout, A. Samat, R. Faure and J. Elguero Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . compound 4 C12H24N4O2 ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 3935-3937 A convenient synthesis of chiral dioxocyclens and application as chiral solvating agents Quan Yuan, Enqin Fu, Xiaojun Wu, Maohai Fang, Peng Xue, Chengtai Wu, Jiahua Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . diethyl 4-methylenespiro[4.5]decane-2,2-dicarboxylate C17H26O4 ÏàËÆ¶È:50% Molecules 2012 17 4313-4325 Communication: New Methodology for the Synthesis of Thiobarbiturates Mediated by Manganese(III) Acetate Ahlem Bouhlel, Christophe Curti and Patrice Vanelle Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 2-[2-(octylamino)-2-oxoethoxy]acetic acid C12H22NO4 ÏàËÆ¶È:50% European Journal of Organic Chemistry 2011 3959-3969 Hydrolysis and Radiation Stability of m-Xylylene Bis-diglycolamide: Synthesis and Quantitative Study of Degradation Products by HPLC¨CAPCI+ Hitos Gal¨¢n, Mar¨ªa Teresa Murillo, Rosa Sedano, Ana N¨²ñez, Javier de Mendoza, Amparo Gonz¨¢lez-Espartero and Pilar Prados Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . compound S7 C15H34O3Si ÏàËÆ¶È:50% Journal of the American Chemical Society 2006 128 11906-11915 Synthetic Studies of Complex Immunostimulants from Quillaja saponaria: Synthesis of the Potent Clinical Immunoadjuvant QS-21Aapi Yong-Jae Kim, Pengfei Wang, Mauricio Navarro-Villalobos, Bridget D. Rohde, JohnMark DerryBerry, and David Y. Gin Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 2-O-(1',2'-dipentanoyl-sn-glycero)-2-thioxo-2¦Ë5-[1,3,2]-dithiaphospholane C15H27O5PS3 ÏàËÆ¶È:50% The Journal of Organic Chemistry 2003 68 7298-7307 Design, Synthesis, and Evaluation of Water-Soluble Phospholipid Analogues as Inhibitors of Phospholipase C from Bacillus cereus Christopher L. Franklin, Hui Li, and Stephen F. Martin Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . TFA¡¤Me2N-D-Ile-Hic-OH C14H27NO4 ÏàËÆ¶È:50% Chemistry-A European Journal 2011 17 13544-13552 Total Synthesis, Stereochemical Assignment, and Antimalarial Activity of Gallinamide A Trent Conroy, Jin T. Guo, Prof. Roger G. Linington, Prof. Nicholas H. Hunt and Dr. Richard J. Payne Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . (4R,2'S)-4-(2'-Hydroxyheptyl)-N(5)-methyl-1,5-diazocan-2-one C14H28N2O2 ÏàËÆ¶È:50% The Journal of Organic Chemistry 2012 77 9724-9737 Absolute Configuration Assignment by Asymmetric Syntheses of the Homalium Alkaloids (− -(R,R,R)-Hoprominol and (− -(4¡äS,4¡åR,2‴R)-HopromalinolStephen G. Davies, James A. Lee, Paul M. Roberts, Jeffrey P. Stonehouse, and James E. Thomson Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-07-13 16:39:50














»Ø¸´´ËÂ¥
-(R,R,R)-Hoprominol and (−