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| 氘代丙酮作谱：197.3， 162.7， 155.8， 138.2， 134.3， 128.4， 127.2， 124.8， 123.1， 75.3， 72.3， 68.9， 63.6， 55.0， 53.4， 49.3， 45.5， 36.6， 36.0， 35.5， 33.9， 33.7， 25.2，22.6， 16.4，15.4 |
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至尊木虫 (著名写手)
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至尊木虫 (著名写手)
- 应助: 304 (大学生)
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至尊木虫 (著名写手)
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刘敏8998: 金币+10, ★★★★★最佳答案 2013-12-17 11:10:17
刘敏8998: 金币+10, ★★★★★最佳答案 2013-12-17 11:10:17
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查询结果：共查到136个化合物(查询结果仅供参考) 1 . 12β,15α,25,28-tetrahydroxyergosta-4,6,8(14),22-tetraen-3-one C28H40O5 相似度:92.8% Helvetica Chimica Acta 2012 95 308-313 Highly Conjugated Ergostane-Type Steroids and Aranotin-Type Diketopiperazines from the Fungus Aspergillus terreus BCC 4651 Rachada Haritakun, Pranee Rachtawee, Somjit Komwijit, Sutichai Nithithanasilp,and Masahiko Isaka Structure 13C NMR 碳谱模拟图 2 . 12β,15α,25,26-tetrahydroxyergosta-4,6,8(14),22-tetraen-3-one C28H40O5 相似度:71.4% Helvetica Chimica Acta 2012 95 308-313 Highly Conjugated Ergostane-Type Steroids and Aranotin-Type Diketopiperazines from the Fungus Aspergillus terreus BCC 4651 Rachada Haritakun, Pranee Rachtawee, Somjit Komwijit, Sutichai Nithithanasilp,and Masahiko Isaka Structure 13C NMR 碳谱模拟图 3 . 17β-[3-(N-Phenyl)-2-oxazolidon-5-yl]androst-4-en-3-one 相似度:57.6% Steroids 2008 73 1375-1384 Neighboring group participation: Part 17 Stereoselective synthesis of some steroidal 2-oxazolidones, as novel potential inhibitors of 17α-hydroxylase-C17,20-lyase Dóra Ondré, János Wölfling, Zoltán Iványi, Gyula Schneider, István Tóth, Mihály Szécsi, János Julesz Structure 13C NMR 碳谱模拟图 4 . 17β-(1-p-Chlorophenyl-3-pyrazolyl)androst-4-en-3-one C28H33ClN2O 相似度:57.6% Steroids 2010 75 450-456 Synthesis of regioisomeric 17β-N-phenylpyrazolyl steroid derivatives and their inhibitory effect on 17α-hydroxylase/C17,20-lyase Zoltán Iványi, János Wölfling, Tamás Görbe, Mihály Szécsi, Tibor Wittmann, Gyula Schneider Structure 13C NMR 碳谱模拟图 5 . 17β-(1-p-Chlorophenyl-5-pyrazolyl)androst-4-en-3-one C28H33ClN2O 相似度:57.6% Steroids 2010 75 450-456 Synthesis of regioisomeric 17β-N-phenylpyrazolyl steroid derivatives and their inhibitory effect on 17α-hydroxylase/C17,20-lyase Zoltán Iványi, János Wölfling, Tamás Görbe, Mihály Szécsi, Tibor Wittmann, Gyula Schneider Structure 13C NMR 碳谱模拟图 6 . compound 16b C32H50O4 相似度:57.6% Journal of the Chemical Society, Perkin Transactions 1 1989 165-174 Synthetic photochemistry. Part 44. Total synthesis of ceroplastol II and albolic acid, 5-8-5-membered tricyclic sesterterpenoid insect wax constituents, via stereocontrolled silyloxy-Cope rearrangement with a normally disfavoured transition state Nobuo Kato, Hitoshi Takeshita, Hideo Kataoka, Shoji Ohbuchi and Shinya Tanaka Structure 13C NMR 碳谱模拟图 7 . agelasidine E C23H41N3O3S 相似度:57.6% European Journal of Organic Chemistry 2012 5131-5135 Antifungal Diterpene Alkaloids from the Caribbean Sponge Agelas citrina: Unified Configurational Assignments of Agelasidines and Agelasines E. Paige Stout, Lily C. Yu and Tadeusz F. Molinski Structure 13C NMR 碳谱模拟图 8 . 16-O-phenylthiomethylliphagal C29H34O4S 相似度:55.5% Organic Letters 2010 Vol.12,No.20 4450-4453 Enantioselective Total Synthesis of the Selective PI3 Kinase Inhibitor Liphagal Enrique Alvarez-Manzaneda, Rachid Chahboun, Esteban Alvarez, Ma José Cano, Ali Haidour, and Ramón Alvarez-Manzaneda Structure 13C NMR 碳谱模拟图 9 . (6β,8aβ)-N,N-Dimethyl-1,2,3,5,6,7,8,8a-octahydro-2-(3-phenyl-2- propen-1-yl)-5,5,8a-trimethyl-6-isoquinolineamine C23H34N2· 2C7H8O3S 相似度:53.8% Chemical & Pharmaceutical Bulletin 2002 50(3) 316-329 Structure Activity Relationships of New Inhibitors of Mammalian 2,3-Oxidosqualene Cyclase Designed from Isoquinoline Derivatives Jean BINET, Didier THOMAS, Abdellah BENMBAREK, Daniel de FORNEL, and Patrice RENAUT Structure 13C NMR 碳谱模拟图 10 . 13-epi-yosgadensonol 相似度:53.8% Journal of Natural Products 1996 59 113-116 Norditerpenes and Norsesterterpenes from Salvia yosgadensis Gülacüti Topç, and Ayhan Ulubelen Structure 13C NMR 碳谱模拟图 11 . 17α,21-Dihydroxy-pregna-4,6-diene-3,11,20-trione21-acetate C23H28O6 相似度:53.8% Steroids 2005 70 763-769 A concise method for the preparation of deuterium-labeled cortisone: Synthesis of [6,7-2H]cortisone Agnieszka Sulima, Thomas E. Prisinzano, Thomas Spande, Jeffrey R. Deschamps, Noel Whittaker, Zeev Hochberg, Arthur E. Jacobson, Kenner C. Rice Structure 13C NMR 碳谱模拟图 12 . 17β-[3-(N-4-Chlorophenyl)-2-oxazolidon-5-yl]androst-4-en-3-one 相似度:53.8% Steroids 2008 73 1375-1384 Neighboring group participation: Part 17 Stereoselective synthesis of some steroidal 2-oxazolidones, as novel potential inhibitors of 17α-hydroxylase-C17,20-lyase Dóra Ondré, János Wölfling, Zoltán Iványi, Gyula Schneider, István Tóth, Mihály Szécsi, János Julesz Structure 13C NMR 碳谱模拟图 13 . (5'R)-17β-[2-(4-nitrophenyl)-4,5-dihydrooxazol-5-yl]androst-5-en-3-one C28H34N2O2 相似度:53.8% Steroids 2009 74 1025-1032 Steroselective synthesis of some steroidal oxazolines, as novel potential inhibitors of 17α-hydroxylase-C17,20-lyase Dóra Ondré, János Wölfling, István Tóth, Mihály Szécsi, János Julesz, Gyula Schneider Structure 13C NMR 碳谱模拟图 14 . 17β-(1-Phenyl-3-pyrazolyl)androst-4-en-3-one C28H34N2O 相似度:53.8% Steroids 2010 75 450-456 Synthesis of regioisomeric 17β-N-phenylpyrazolyl steroid derivatives and their inhibitory effect on 17α-hydroxylase/C17,20-lyase Zoltán Iványi, János Wölfling, Tamás Görbe, Mihály Szécsi, Tibor Wittmann, Gyula Schneider Structure 13C NMR 碳谱模拟图 15 . 17β-(1-p-Cyanophenyl-3-pyrazolyl)androst-4-en-3-one C29H33N3O 相似度:53.8% Steroids 2010 75 450-456 Synthesis of regioisomeric 17β-N-phenylpyrazolyl steroid derivatives and their inhibitory effect on 17α-hydroxylase/C17,20-lyase Zoltán Iványi, János Wölfling, Tamás Görbe, Mihály Szécsi, Tibor Wittmann, Gyula Schneider Structure 13C NMR 碳谱模拟图 16 . longipin-2-ene-7β,9α-diol-1-one diangelate 相似度:53.8% Phytochemistry 1989 28 265-268 Isolation and preparation of two longipinene derivatives from Stevia subpubescens Luisa U. Román,Juan D. Hernández,Raúl Castañeda,Carlos M. Cerda,Pedro Joseph-Nathan Structure 13C NMR 碳谱模拟图 17 . 2α,15,16-trihydroxy-ent-pimar-7-en C20H34O3 相似度:53.8% Phytochemistry 1990 29 573-577 Ent-pimarene derivatives from Palafoxia arida C. Zdero,F. Bohlmann,R.M. King Structure 13C NMR 碳谱模拟图 18 . (3S,4R)-3-((3E,7E)-8-Iodo-3,7-dimethylocta-3,7-dienyl)-2-(4-methoxybenzyloxymethyl)-3,4-dimethylcyclohex-1-enecarbaldehyde C28H39IO3 相似度:53.8% Organic & Biomolecular Chemistry 2004 2 466-473 Total synthesis of (±)-phomactin G, a platelet activating factor antagonist from the marine fungus Phoma sp. William P. D. Goldring and Gerald Pattenden Structure 13C NMR 碳谱模拟图 19 . (3E,7E)-(1R,2R,11S,12R,16S)-16-(4-Methoxybenzyloxymethyl)-4,8,11,12-tetramethyl-15-oxatricyclo[9.3.2.01,16]hexadeca-3,7-dien-2-ol C28H40O4 相似度:53.8% Organic & Biomolecular Chemistry 2004 2 466-473 Total synthesis of (±)-phomactin G, a platelet activating factor antagonist from the marine fungus Phoma sp. William P. D. Goldring and Gerald Pattenden Structure 13C NMR 碳谱模拟图 20 . compound 15 C27H42O3 相似度:53.8% Journal of the Chemical Society, Perkin Transactions 1 1989 165-174 Synthetic photochemistry. Part 44. Total synthesis of ceroplastol II and albolic acid, 5-8-5-membered tricyclic sesterterpenoid insect wax constituents, via stereocontrolled silyloxy-Cope rearrangement with a normally disfavoured transition state Nobuo Kato, Hitoshi Takeshita, Hideo Kataoka, Shoji Ohbuchi and Shinya Tanaka Structure 13C NMR 碳谱模拟图 21 . gephyronic acid hemiketal(β) C26H46O7 相似度:53.8% Angewandte Chemie International Edition 2011 50 938-941 Gephyronic Acid, a Missing Link between Polyketide Inhibitors of Eukaryotic Protein Synthesis (Part I): Structural Revision and Stereochemical Assignment of Gephyronic Acid Lionel Nicolas, Timo Anderl, Florenz Sasse, Heinrich Steinmetz, Rolf Jansen, Gerhard H fle, Sabine Laschat, and Richard E. Taylor Structure 13C NMR 碳谱模拟图 |
6楼2013-12-13 16:23:34