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fly5fish

木虫 (正式写手)

[求助] 求微谱gsh2


C:10.4,13.1,18.6,19.9,21.3,21.5,22.8,23.5,23.6,25.9,30.3,32.7,36.7,37.3,38.8,38.9,42.1,50.0,54.6,57.5,57.7,61.1,67.4,122.0,128.8,130.5,131.2,132.6,134.9,135.9,167.1,170.0     溶剂为氘代丙酮,谢谢
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呢喃-21

银虫 (小有名气)

【答案】应助回帖

★ ★ ★ ★ ★ ★ ★ ★ ★ ★
感谢参与,应助指数 +1
fly5fish(豆哥代发): 金币+10, 谢谢 2013-12-07 15:48:23
查询模式:模糊查询
碳谱数据输入:
按从小到大顺序输入,数字间用英文半角逗号(,)分隔例如:
21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

溶剂选项:
匹配容差: (数字格式,可自行设定)
相似度:   %(相似度>=50%)



查询结果:共查到2513个化合物(查询结果仅供参考)
1 .     (17E)-3β-acetoxy-17-(3-Oxa-1-azaspiro[4.5]dec-1-en-2-ylmethylene)androst-5-ene
C30H43NO3     相似度:65.6%
Steroids          2012          77          77-84
Synthesis of 21-nitrogen substituted pregna-5,17(20)-dienes from pregnenolone
Sergey V. Stulov, Yaroslav V. Tkachev, Roman A. Novikov, Maria G. Zavialova, Vladimir P. Timofeev, Alexander Yu. Misharin
Structure      13C NMR   碳谱模拟图
2 .     3β-p-Tolylsulfanylcholest-5-ene
C34H52S     相似度:65.6%
Tetrahedron          2013          69          8904-8913
Electrochemical synthesis of glycoconjugates of 3β-hydroxy-Δ5-steroids by using non-activated sugars and steroidal thioethers
Aneta M. Tomkiel, Krzysztof Brzezinski, Zenon Łotowski, Leszek Siergiejczyk, Piotr Wałejko, Stanisław Witkowski, Jan Kowalski, Jolanta Płoszyńska, Andrzej Sobkowiak, Jacek W. Morzycki
Structure      13C NMR   碳谱模拟图
3 .     1' ,4' ,16,17-Tetrahydro-3β-acetoxy-1' -acetyl-6' -bromo-4 '-methyl-(16α,17α)-androsta-5,16-dieno[17,16-b]quinoline
C31H40BrNO3     相似度:62.5%
Steroids          2004          69          301-312
Synthesis of novel steroid-tetrahydroquinoline hybrid molecules and -homosteroids by intramolecular cyclization reactions
Angéla Magyar, János Wölfling, Melanie Kubas, Jose Antonio Cuesta Seijo, Madhumati Sevvana, Regine Herbst-Irmer, Péter Forgó, Gyula Schneider
Structure      13C NMR   碳谱模拟图
4 .     3β-acetoxy-21-chloromethylpregn-5-ene-20β-N-phenylurethane
C32H44O4NCl     相似度:62.5%
Steroids          2004          69          451-460
Neighboring group participation: Part 15. Stereoselective synthesis of some steroidal tetrahydrooxazin-2-ones, as novel presumed inhibitors of human 5α-reductase
János Wölfling, László Hackler, Erzsébet Mernyák, Gyula Schneider, István Tóth, Mihály Szécsi, János Julesz, Pál Sohár, Antal Csámpai
Structure      13C NMR   碳谱模拟图
5 .     5α,6β-Dibromocholestan-3β-yl benzoate
    相似度:62.5%
Steroids          2005          70          867-872
Electrochemical bromination of cholest-5-enes
Smiljka S. Milisavljević, Klaus Wurst, Gerhard Laus, Mirjana D. Vukićević, Rastko D. Vukićević
Structure      13C NMR   碳谱模拟图
6 .     3β-Acetoxy-17β-[2' -(4''-chlorophenyl)-4' ,5' -dihydro-6' H-1 ,3' -oxazin-6' -yl] androst-5-ene
C31H40O3NCl     相似度:62.5%
Steroids          2006          71          809-816
Stereoselective synthesis of some 17β-dihydrooxazinyl steroids, as novel presumed inhibitors of 17α-hydroxylase-C17,20-lyase
János Wölfling, éva Andrea Oravecz, Dóra Ondré, Erzsébet Mernyák, Gyula Schneider, István Tóth, Mihály Szécsi, János Julesz
Structure      13C NMR   碳谱模拟图
7 .     3β-Acetoxy-17β-[2'-(4' '-bromophenyl)-4' ,5' -dihydro-6' H-1' ,3' -oxazin-6' -yl] androst-5-ene
C31H40O3NCl     相似度:62.5%
Steroids          2006          71          809-816
Stereoselective synthesis of some 17β-dihydrooxazinyl steroids, as novel presumed inhibitors of 17α-hydroxylase-C17,20-lyase
János Wölfling, éva Andrea Oravecz, Dóra Ondré, Erzsébet Mernyák, Gyula Schneider, István Tóth, Mihály Szécsi, János Julesz
Structure      13C NMR   碳谱模拟图
8 .     3β-Acetoxy-17β-[2'-(phenyl)-5',6'-dihydro-4'H-1',3'-oxazin-4'-yl]androst-5-ene
C31H41O3N     相似度:62.5%
Steroids          2006          71          809-816
Stereoselective synthesis of some 17β-dihydrooxazinyl steroids, as novel presumed inhibitors of 17α-hydroxylase-C17,20-lyase
János Wölfling, éva Andrea Oravecz, Dóra Ondré, Erzsébet Mernyák, Gyula Schneider, István Tóth, Mihály Szécsi, János Julesz
Structure      13C NMR   碳谱模拟图
9 .     3β-Acetoxy-17β-[2'-(4''-chlorophenyl)-5',6'-dihydro-4' H-1',3'-oxazin-4'-yl]androst-5-ene
C31H40O3NCl     相似度:62.5%
Steroids          2006          71          809-816
Stereoselective synthesis of some 17β-dihydrooxazinyl steroids, as novel presumed inhibitors of 17α-hydroxylase-C17,20-lyase
János Wölfling, éva Andrea Oravecz, Dóra Ondré, Erzsébet Mernyák, Gyula Schneider, István Tóth, Mihály Szécsi, János Julesz
Structure      13C NMR   碳谱模拟图
10 .     3β-Acetoxy-17β-[2 -(3'' ,4 '' ,5'' -trimethoxyphenyl)-5' ,6' -dihydro-4' H-1' ,3' -oxazin-4 '-yl]androst-5-ene
C34H47O6N     相似度:62.5%
Steroids          2006          71          809-816
Stereoselective synthesis of some 17β-dihydrooxazinyl steroids, as novel presumed inhibitors of 17α-hydroxylase-C17,20-lyase
János Wölfling, éva Andrea Oravecz, Dóra Ondré, Erzsébet Mernyák, Gyula Schneider, István Tóth, Mihály Szécsi, János Julesz
Structure      13C NMR   碳谱模拟图
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