部分構造検索

12950

COC(=O)c1sccc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #69919
4-(2-methoxycarbonylthiophen-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid t-butyl ester
収率 34.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sccc1C1CCN(C(=O)OC(C)(C)C)CC1
Reaction #69920
4-(2-methoxycarbonylthiophen-3-yl)piperidine-1-carboxylic acid t-butyl ester
収率 95.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(c2ccsc2CO)CC1
Reaction #69921
title compound
収率 68.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1sc(Br)cc1CCCl
Reaction #156687
5-Bromo-3-(2-chloro-ethyl)-thiophene-2-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)c1cc2c(s1)C(=O)OCC2
Reaction #156688
2-Trimethylsilanyl-4,5-dihydro-thieno[2,3-c]pyran-7-one
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)c1cc(CCO)c(C(=O)O)s1
Reaction #156689
3-(2-Hydroxy-ethyl)-5-trimethylsilanyl-thiophene-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2=NOC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)C2)sc1C(=O)NCC(F)(F)F
Reaction #173831
DOI: 10.1039/C8SC04228D
CN(CCc1ccc(F)cc1)S(=O)(=O)c1csc2c1CCCC2=O
Reaction #176418
DOI: 10.1039/C8SC04228D
C#CCNC(=O)NC1CCCC(=O)c2sccc21
Reaction #178108
DOI: 10.1039/C8SC04228D
O=CNC1CCC(=O)c2sccc21
Reaction #183464
DOI: 10.1039/C8SC04228D
CCN(C)S(=O)(=O)c1ccc(-c2cnc(N)c(-c3cc4c(s3)C(=O)NCC4)c2)nc1
Reaction #189542
DOI: 10.1039/C8SC04228D
O=C1NCCc2cc(Br)sc21
Reaction #199181
DOI: 10.1039/C8SC04228D
CCN(C)S(=O)(=O)c1ccc(-c2cnc(N)c(-c3cc4c(s3)C(=O)NC4)c2)nc1
Reaction #199801
DOI: 10.1039/C8SC04228D
Cl
Reaction #202372
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCc2nc3sc4c(c3c(=O)n2CC1)CCCC4=O
Reaction #204361
DOI: 10.1039/C8SC04228D
CN(CC(O)c1ccc(N2CCCC2)cc1)S(=O)(=O)c1csc2c1CCCC2=O
Reaction #206672
DOI: 10.1039/C8SC04228D
CC(C)(C)CCc1ccsc1CN
Reaction #210652
DOI: 10.1039/C8SC04228D
Cc1csc2c1CCOC2=O
Reaction #221324
DOI: 10.1039/C8SC04228D
[C-]#[N+]C1CCC(=O)c2sccc21
Reaction #223993
DOI: 10.1039/C8SC04228D
O=C1NCCCc2cc(CCCl)sc21
Reaction #226085
DOI: 10.1039/C8SC04228D
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