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1130277

CC1(C)OCc2cc(C(=O)CBr)ccc2O1
Reaction #42732
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C)CCCN(C(=O)OC(C)(C)C)C1
Reaction #58684
3-methyl-piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester
Выход 95.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCO)Nc1cc(-c2c[nH]nc2-c2cccc(NC(=O)Nc3ccc(C(F)(F)F)cc3)c2)ccn1
Reaction #74140
title compound
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C/C(=O)N1C(=O)OC[C@@H]1c1ccccc1
Reaction #81626
title compound
Выход 28.7%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(C2COC2)cc(F)n1
Reaction #86247
2,6-difluoro-4-(oxetan-3-yl)pyridine
Выход 390.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)c1cc2c(s1)-c1ccccc1OCC2)c1ncccc1Cl
Reaction #171690
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COCC#Cc1ccc(Nc2c(C#N)cnc3cc(OCCCN4CCN(C)CC4)c(OC)cc23)c2occc12
Reaction #434503
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc2ncc(C#N)c(Nc3ccc(C#CCOC)c4c3OCO4)c2cc1OC.Cl
Reaction #434608
title compound
Выход 69.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCC(=COC)CC1
Reaction #466269
title compound
Выход 89.4%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(CC2CCCCO2)cc1
Reaction #536305
2-(4-Chloro-benzyl)-tetrahydropyran
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(CC2CCCO2)cc1
Reaction #536311
2-(4-Chloro-benzyl)-tetrahydrofuran
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Oc3ccc4[nH]c(C)cc4c3)ncnc2cc1C=CC(=O)O
Reaction #541257
7-(2-carboxyvinyl)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline
Выход 71.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)c1ccc(OC)c(B2OC(C)(C)C(C)(C)O2)c1
Reaction #543395
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1[C@@H](c2cc(C(F)(F)F)cc(C(F)(F)F)c2)OC(=O)N1Cc1cc(C(F)(F)F)ccc1Br
Reaction #543401
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCc2cc(C(=O)CBr)ccc2O1
Reaction #578175
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\[C@H]1CC[C@@H](NC(=O)OC(C)(C)C)CC1
Reaction #587259
t-butyl cis-4-[(Z)-1-butenyl]cyclohexylcarbamate
Выход 40.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(COc1ccc2ncccc2c1)OC
Reaction #587326
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(C2COC2)cc1
Reaction #598846
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccnnc1)c1ccc(F)cc1
Reaction #602744
pale yellow powder
Выход 77.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@H]1[C@H]2CC[C@H](CCCC(=O)OC(C)C)CO[C@H]2C[C@H]1OC1CCCCO1
Reaction #660716
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
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