Поиск подструктуры

188

CC1(CNc2ncccc2Cl)COC1
Reaction #736
Выход 12.2%
Cc1nn(CC2(C)COC2)c(C)c1Br
Reaction #86334
title compound
Выход 49.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(CC2(C)COC2)c(C)c1-c1cc(C(F)(F)F)cc2[nH]ncc12
Reaction #86385
title compound
Выход 28.5%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc2nc(C#N)c(N3CC4(COC4)C3)cc21
Reaction #162494
title compound
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)c1nc2ccn(C)c2cc1N1CC2(COC2)C1
Reaction #162495
title compound
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1nc(N)nc(N)c1C#N)c1nc2ccn(C)c2cc1N1CC2(COC2)C1
Reaction #162525
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1C(=O)/N=c1\sc(C(C)(C)C)cn1CC1(C)COC1
Reaction #165692
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N2CC3(COC3)C2)cn1
Reaction #170370
title compound
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #172910
solid
Выход 18.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #172911
oil
Выход 12.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(CN2Cc3nc(Nc4sc(-c5c(F)cc(C(C)(C)O)cc5F)cc4C(N)=O)ccc3C2=O)COC1
Reaction #186194
DOI: 10.1039/C8SC04228D
CC1(Cn2cc(Br)cn2)COC1
Reaction #195804
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NCC1(CO)COC1
Reaction #206545
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NCC1(CO)COC1
Reaction #222527
DOI: 10.1039/C8SC04228D
O=C(c1ccc(N2CCCC2)c(OCC2CC2)n1)N1CC2(COC2)C1
Reaction #255551
DOI: 10.1039/C8SC04228D
Brc1ccc(CN2CC3(COC3)C2)cc1
Reaction #273029
DOI: 10.1039/C8SC04228D
CNCC1(C2CCCCC2)COC1
Reaction #277226
DOI: 10.1039/C8SC04228D
Cc1nc2ccccc2n1-c1nc(N2CCOCC2)c2nc(CNCC3(C)COC3)n(C)c2n1
Reaction #295979
DOI: 10.1039/C8SC04228D
CC1(CN=[N+]=[N-])COC1
Reaction #347031
3-azidomethyl-3-methyloxetane
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCC1(COc2ccccc2)COC1
Reaction #347032
3-azidomethyl-3-phenoxymethyloxetane
Выход 87.0%DOI: 10.6084/m9.figshare.5104873.v1
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