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41198

CC(=O)NCC1=CC=C(CO)SS1
Reaction #231420
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NCC1=CC=C(CCl)SS1
Reaction #247342
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OCC1=CC=C(COc2ccccc2C(F)(F)F)SS1
Reaction #251457
DOI: 10.1039/C8SC04228D
CN(C)c1cccc(OCC2=CC=CSS2)c1
Reaction #352492
6-[[3-(N,N-dimethylamino)-phenyloxy]methyl]-1,2-dithiin
収率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1cccc(OCC2=CC=C(CO)SS2)c1
Reaction #352493
title compound
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCC1=CC=C(COc2ccccc2C(F)(F)F)SS1
Reaction #352494
3-[(tert-butyldimethylsilyloxy)methyl]-6-[(2-trifluoromethylphenyloxy)methyl]-1,2-dithiin
収率 37.0%DOI: 10.6084/m9.figshare.5104873.v1
OCC1=CC=C(COc2ccccc2C(F)(F)F)SS1
Reaction #352495
title compound
収率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
OCC1=CC=C(COc2ccccc2F)SS1
Reaction #352496
title compound
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cccc(OCC2=CC=CSS2)c1
Reaction #352497
6-[(3-ethynylphenyloxy)methyl]-1,2-dithiin
収率 56.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2nc(C3=CC=C(CO[Si](C)(C)C(C)(C)C)SS3)c(O)nc12
Reaction #352498
3-[(tert-butyldimethylsilyloxy)methyl]-6-[methyloxy[3-hydroxyquinoxalin-2-yl]]-1,2-dithiin
収率 28.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2nc(C3=CC=C(CO)SS3)c(O)nc12
Reaction #352499
title compound
収率 51.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCC1=CC=C(COc2cc(C(F)(F)F)ccc2Cl)SS1
Reaction #352500
3-[(tert-butyldimethylsilyloxy)methyl]-6-[(2-chloro-5-trifluoromethyl-phenyloxy)methyl]-1,2-dithiin
DOI: 10.6084/m9.figshare.5104873.v1
OCC1=CC=C(COc2cc(C(F)(F)F)ccc2Cl)SS1
Reaction #352501
title compound
収率 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CSN1NN=C(C2=CC=C(CO)SS2)N1c1ccc(O)cc1
Reaction #352502
title compound
収率 79.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC1=CC=C(CO)SS1)c1ccccc1
Reaction #352503
title compound
収率 53.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC1=CC=C(COC(=O)C2CC2)SS1)C1CC1
Reaction #830274
oil
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCC1=CC=C(COc2cc(C(F)(F)F)ccc2Cl)SS1
Reaction #911128
DOI: 10.1039/C8SC04228D
O=C(NCC1=CC=C(CO)SS1)c1ccccc1O
Reaction #1043886
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OCC1=CC=C(C=O)SS1
Reaction #1166939
aldehyde
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCC1=CC=C(CN=[N+]=[N-])SS1
Reaction #1168077
azide
収率 74.5%DOI: 10.6084/m9.figshare.5104873.v1
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