Substructure Search

CC1(O)CCCCC1

CN(C)C1C(O)=C(C(N)=O)C(=O)C2(O)C(O)=C3C(=O)c4c(O)ccc(Br)c4CC3CC12.O=S(=O)(O)O
Reaction #6539
pure product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CC3CC(C2)CC1C3
Reaction #9839
2-adamantanon
DOI: 10.6084/m9.figshare.5104873.v1
ON=C1C2CC3CC1CC(O)(C3)C2
Reaction #41094
5-hydroxy-adamantan-2-one oxime
Yield 73.4%DOI: 10.6084/m9.figshare.5104873.v1
NC1C2CC3CC1CC(O)(C3)C2
Reaction #41095
4-amino-adamantan-1-ol
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1C2CC3CC1CC(O)(C3)C2
Reaction #41096
4-amino-adamantan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CCCC2SCC(=O)N2CCC2(O)CCCCC2)cc1
Reaction #56484
title compound
Yield 32.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CCCC2SCC(=O)N2CCC2(O)CCCCC2)cc1
Reaction #56485
4-{3-[3-[2-(1-Hydroxycyclohexyl)-ethyl]-4-oxo-2-thiazolidinyl]propyl}benzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CCCC2SCC(=O)N2CCC2(O)CCCCC2)cc1
Reaction #56487
4-{3-[3-[2-(1-Hydroxycyclohexyl)ethyl]-4-oxo-2-thiazolidinyl]propyl}benzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CCCC2N(CCC3(O)CCCCC3)C(=O)CS2=O)cc1
Reaction #56488
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cccc(Cl)c1
Reaction #56489
m-chlorobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(CCCC2SCC(=O)N2CCC2(O)CCCCC2)c(Cl)c1
Reaction #56490
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(CCCC2SCC(=O)N2CCC2(O)CCCCC2)c(C)c1
Reaction #56492
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CCCC2SCC(=O)N2CCCC2(O)CCCCC2)cc1
Reaction #56497
title product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CCCC2SCC(=O)N2CCC2(O)CCCCC2)cc1
Reaction #56499
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NC(=O)c1ccc(CCCC2SCC(=O)N2CCC2(O)CCCCC2)cc1
Reaction #56501
N-Methylsulfonyl-4-{3-[3-[2-(1-hydroxycyclohexyl)ethyl]-4-oxo-2-thiazolidinyl]propyl}benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1(CCN2C(=O)CSC2CCCc2ccc(C(=O)O)cc2)CCCCC1
Reaction #56502
4-{3-[3-[2-(1-Acetoxycyclohexyl)ethyl]-4-oxo-2-thiazolidinyl]propyl}benzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CN[C@H]1CCN(C2CCCCC2(O)C(C)c2cccc(C(F)(F)F)c2)C1.Cl.Cl
Reaction #57103
2-[(3S)-3-(methylamino)pyrrolidin-1-yl]-1-[3-(trifluoromethyl)phenyl]ethylcyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(N)C2CC3CC1CC(O)(C3)C2
Reaction #66725
4-allyl-4-amino-adamantan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C12CC3CC(C1)C(=O)C(C3)C2
Reaction #66728
desired product
DOI: 10.6084/m9.figshare.5104873.v1
NC1C2CC3CC1CC(Oc1cc4ccnc(OCc5ccccc5)c4cc1Cl)(C3)C2
Reaction #66732
title compound
Yield 31.2%DOI: 10.6084/m9.figshare.5104873.v1
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