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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½89¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 9bac C96H96N4O10 ÏàËÆ¶È:61.2% Tetrahedron 2012 68 6323-6328 Synthesis of upper rim N-formamido and isocyanocalix[4]arenes: adaptation of Ugi-4-CR on calix[4]arenes towards peptide-like architectures Anupriya Savithri, Sreeja Thulasi, Luxmi Varma Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (1S,5S,7R,9R,13S,15S,16R)-15-(benzyloxy)-5-(hydroxymethyl)-7-[(p-methoxybenzyl)oxy]-6,6,9,16-tetramethyl-11-(phenylsulfonyl)-4,-17-dioxabicyclo[11.3.1]heptadecane-3,10-dione ÏàËÆ¶È:60.6% Journal of the American Chemical Society 2000 122 619-631 Stereocontrolled Elaboration of Natural (− -Polycavernoside A, a Powerfully Toxic Metabolite of the Red Alga Polycavernosa tsudaiLeo A. Paquette, Louis Barriault, Dmitri Pissarnitski, and Jeffrey N. Johnston Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (E/Z)-Methyl 2-[(RS)-1-(4-methoxyphenyl)-2-oxo-4-phenylazetidin-3-ylidene]propionate C20H19NO4 ÏàËÆ¶È:58.0% Pharmazie 2001 56 686-690 ¦Â-Lactam derivatives as enzyme inhibitors: Derivatives of (E)-2-[(RS)-1-(4-methoxyphenyl)-2-oxo-4-phenylazetidin-3-ylidene]propionic acid C. Venz - H.-H. Otto Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 1,4-diphenyl-2,3-bis(dimethylene formate)-9,9'-spirobifluorene ÏàËÆ¶È:58.0% Heterocycles 2012 85 1077-1088 Synthesis of Fluorene- and Spirobifluorene-Fused Thiophenes Wen Yao, Qiancai Liu,* Yingbo Shi, and Jie Tang Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 1,3-Dibenzyl-7-bromo-9-chloro-5-phenethyl-2,3,4,5-tetrahydro-1H-chromeno[4,3-d]pyrimidine C33H31BrClN2O ÏàËÆ¶È:58.0% Tetrahedron 2012 68 7035-7040 Proline-mediated formation of novel chroman-4-one tetrahydropyrimidines Maria Frid¨¦n-Saxin, Tina Seifert, Lars Kristian Hansen, Morten Grøtli, Mate Erdelyi, Kristina Luthman Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . N-Benzyl-2-bromo-4-((S)-2-((S)-2-(4-cyanobenzamido)-3-(4-hydroxyphenyl)propanamido)-4-methylpentanamido)-benzamide C37H36BrN5O5 ÏàËÆ¶È:54.8% Bioorganic & Medicinal Chemistry 2011 19 1823-1838 Design, synthesis and in vitro characterization of novel hybrid peptidomimetic inhibitors of STAT3 protein Vijay M. Shahani, Peibin Yue, Steven Fletcher, Sumaiya Sharmeen, Mahadeo A. Sukhai,Diana P. Luu, Xiaolei Zhang, Hong Sun, Wei Zhao, Aaron D. Schimmer,James Turkson, Patrick T. Gunning Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 6-[6-phenyl-2,2-di(ethoxycarbonyl)indan-5-yl]-7-benzyl-7H-purine C33H30N4O4 ÏàËÆ¶È:54.8% Heterocycles 2010 82 895-907 [2+2+2]-Cocyclotrimerization of 6-Alkynyl-7-benzylpurines with ¦Á,¦Ø-Diynes Stanislav Opekar, Pavel Turek, Radek Pohl, Blanka Klepet¨¢řov¨¢, Ivan Votruba, Michal Hocek, and Martin Kotora Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Compound 5 ÏàËÆ¶È:54.8% Magnetic Resonance in Chemistry 2005 43 1032-1039 Structure elucidation and total synthesis of a unique group of trace impurities in Tipranavir® drug product Carl A. Busacca, Scot Campbell, Anjan Saha, Jon C. Lorenz, Karl Grozinger, Paul-James Jones, Nelu Grinberg, Sherry Shen, Heewon Lee, Fenghe Qiu, Alice Granger, Zhanna Yuabova, Dan Norwood and Chris H. Senanayake Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Compound 6 ÏàËÆ¶È:54.8% Magnetic Resonance in Chemistry 2005 43 1032-1039 Structure elucidation and total synthesis of a unique group of trace impurities in Tipranavir® drug product Carl A. Busacca, Scot Campbell, Anjan Saha, Jon C. Lorenz, Karl Grozinger, Paul-James Jones, Nelu Grinberg, Sherry Shen, Heewon Lee, Fenghe Qiu, Alice Granger, Zhanna Yuabova, Dan Norwood and Chris H. Senanayake Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Compound 9 ÏàËÆ¶È:54.8% Magnetic Resonance in Chemistry 2005 43 1032-1039 Structure elucidation and total synthesis of a unique group of trace impurities in Tipranavir® drug product Carl A. Busacca, Scot Campbell, Anjan Saha, Jon C. Lorenz, Karl Grozinger, Paul-James Jones, Nelu Grinberg, Sherry Shen, Heewon Lee, Fenghe Qiu, Alice Granger, Zhanna Yuabova, Dan Norwood and Chris H. Senanayake Structure 13C NMR ̼Æ×Ä£Äâͼ |

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-Polycavernoside A, a Powerfully Toxic Metabolite of the Red Alga Polycavernosa tsudai