子结构搜索

4982

O=C1[C@@H](CCCO)O[C@H](c2ccccc2)c2ccccc2N1Cc1ccccc1
Reaction #1876
trans-1-benzyl-3-(3-hydroxypropyl)-5-phenyl-1,5-dihydro-4,1-benzoxazepin-2(3H)-one
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCOc1ccc(C(O)C(=O)O)c(Cl)c1OCOCCOC
Reaction #2669
[2-chloro-3,4-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]-hydroxy acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC[Si]1(c2ccccc2)CCC(c2cc(F)c(CC(C)CC)c(F)c2)CC1
Reaction #2743
4-(4-n-heptyl-4-phenyl-4-silacyclohexyl)-1-(2-methylbutyl)-2,6-difluorobenzene
收率 140.1%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OCCc1ccccc1CCl
Reaction #2803
title compound
收率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCc1cc(O)ccc1C[C@@H](CO)NC(=O)OC(C)(C)C
Reaction #5450
N-t-butoxycarbonyl-o-(2-methoxyethoxymethyl)tyrosinol
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H](CO)Cc1ccc(OCc2ccccc2)cc1)OCc1ccccc1
Reaction #5821
title compound
收率 99.9%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(C2=CCCCC2)c1
Reaction #7151
3-(cyclohexen-1-yl)-1-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC12CCC(=O)C(c3ccc(/C=C/C(=O)OC)cc3)=C1c1ccc(OC)cc1C2
Reaction #7939
methyl (2E)-3-[4-(9a-butyl-7-methoxy-3-oxo-2,3,9,9a-tetrahydro-1H-fluoren-4-yl)phenyl]-2-propenoate
收率 96.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1Cc2c(ccc(OC)c2C)C1=O
Reaction #7942
2-butyl-5-methoxy-4-methyl-1-indanone
收率 496.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1Cc2c(cc(F)c(OC)c2C)C1=O
Reaction #7987
2-butyl-6-fluoro-5-methoxy-4-methyl-1-indanone
收率 24.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(-c2nnn[nH]2)cc1
Reaction #8645
colorless crystals
收率 70.7%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cccc2nc(NC(=O)NCC)sc12
Reaction #9219
desired compound
收率 24.5%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc2nc(NC(=O)NCC)sc2c1C=C
Reaction #9220
desired compound
收率 39.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1/C=C/CCO)[nH]c1cc(-c3ccccc3Cl)c3c(c12)C(=O)NC3=O
Reaction #11228
( 170 )
收率 95.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)c(C)c([Si](C)(C)C)n2C1CCCC1
Reaction #11513
white crystals
收率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C2=CCC3(CC2)OCCO3)cc1
Reaction #40328
8-(4-fluorophenyl)-1,4-dioxaspiro[4.5]dec-7-ene
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)CCC1c1ccccc1
Reaction #40332
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(N)c([N+](=O)[O-])cc(-c2ccn(C)c(=O)c2)c1F
Reaction #40529
title compound
收率 25.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(OC[C@H](COCc2ccccc2)NC(=O)OC(C)(C)C)c1
Reaction #40680
t-butyl (1S)-2-(benzyloxy)-1-[(3-methylphenoxy)methyl]ethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(CC)cc(C(=O)OC)c1
Reaction #42280
title compound
DOI: 10.6084/m9.figshare.5104873.v1
第 1 页下一页