부분 구조 검색

278213

COc1nccc(N[C@H]2CC[C@@H](C(C)(C)CC(C)(C)C)CC2)c1OC
Reaction #1121
2,3-Dimethoxy-4-[cis-4-(1,1,3,3-tetramethylbutyl)cyclohexylamino]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1ccc(CC(=O)Nc2cccc(C3CCC(C(C)(C)C)CC3)c2)cc1OC
Reaction #7170
N-[3-(4-tert-butylcyclohexan-1-yl)phenyl]-4-ethoxycarbonylmethyloxy 3-methoxyphenylacetamide
수율 75.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CC(=O)Nc2cccc(C3CCC(C(C)(C)C)CC3)c2)ccc1OCCO
Reaction #7177
desired compound
수율 50.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)ON5C(=O)CCC5=O)CCC4(C)C3CCC12C
Reaction #49205
Compound 83
수율 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCNC(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)ON5C(=O)CCC5=O)CCC4(C)C3CCC12C
Reaction #49208
Compound 89
수율 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCNC(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)NCCCCCC(=O)N5CC(O)CC5C(OC(c5ccc(OC)cc5)c5ccc(OC)cc5)c5ccccc5)CCC4(C)C3CCC12C
Reaction #49209
Compound 90
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H](SC3CCNC3)CC1/C(=N/O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12.O=C(O)/C=C/C(=O)O
Reaction #70354
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H](C)/C=C/[C@@H](C)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #96101
ergosterol tosylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H](C)/C=C/[C@@H](C)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #96102
ergosterol tosylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CCC(OC(=O)CCS)CC1
Reaction #181873
DOI: 10.1039/C8SC04228D
CC1=NC(COP(=O)(OC(C)(C)C)OC(C)(C)C)(c2ccc3c(C(F)(F)F)c(OC4CCC(C(C)(C)C)CC4)ccc3c2)CO1
Reaction #182532
DOI: 10.1039/C8SC04228D
O=C(NC1CCN(CCc2ccccc2)C1)C1(C2CCCCC2)CCCC1
Reaction #186333
DOI: 10.1039/C8SC04228D
CC12CC(=O)C3C(CCC4CC(O)CCC43C)C1CCC2C(=O)COCCN1CCOCC1
Reaction #194159
DOI: 10.1039/C8SC04228D
COC(=O)C=C1CCC(C(C)(C)C)CC1
Reaction #195550
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)=CC1CCC(C(C)(C)CC)CC1
Reaction #200216
DOI: 10.1039/C8SC04228D
Cc1ccccc1CSC1CCC2C3CCC4=CC(=O)C=CC4(C)C3C(=O)CC12C
Reaction #206005
DOI: 10.1039/C8SC04228D
CC(C)(C)C1CCC(Oc2ccc3cc(C(CCC(=O)O)[N+](=O)[O-])ccc3c2C(F)(F)F)CC1
Reaction #206063
DOI: 10.1039/C8SC04228D
CCC(CC)(CC=COC(C)(C)C1=CCC2C3=CC=C4CC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C4(C)C3CCC12C)O[Si](CC)(CC)CC
Reaction #206707
DOI: 10.1039/C8SC04228D
CC1(c2ccc3c(C4CC4)c(OC4CCC(C(C)(C)C)CC4)ccc3c2)COC(=O)N1
Reaction #227079
DOI: 10.1039/C8SC04228D
Cc1c(OC2CCC(C(C)(C)C)CC2)ccc2cc(C(C)(N)CO)ccc12
Reaction #246631
DOI: 10.1039/C8SC04228D
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