Substructure Search

C1CCCC(CCC1)N2CCCC2

CC1(C)C(=O)N(C2CCCC(O)CCC2)CC1CO
Reaction #44496
titled product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(Cc2ccc(-c3ccc(O)cc3)cc2Cl)CCN1C1C2CC3CC(C2)CC1C3
Reaction #282593
DOI: 10.1039/C8SC04228D
NC(=O)[C@@H]1CCC(=O)N1C12CC3CC(CC(C3)C1)C2
Reaction #630431
N-[Adamantan-1-yl]-(L)-Pyroglutamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[C@@]1(C(=O)OCc2ccccc2)CCCN1C12CC3CC(CC(C3)C1)C2
Reaction #631446
N-(1-adamantyl)-ethanoylproline benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(C)C=C(C(=O)NCC2CCCN2C2CCCCCCC2)C(OC)C1=S(=O)=O
Reaction #739966
N-(1-cyclooctyl-2-pyrrolidinyl methyl)-2,4-dimethoxy-5-methyl-sulphonyl benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[N+]1(C2CCCCCCC2)CCCC1.[I-]
Reaction #1077761
N-butyl-N-cyclooctylpyrrolidinium iodide
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[N+]1(C2CCCCCCC2)CCCC1.[OH-]
Reaction #1077762
N-butyl-N-cyclooctylpyrrolidinium hydroxide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1C12CC3CC(C1)C(C(=O)O)(C3)C2
Reaction #1102706
1-(2-oxopyrrolidin-1-yl)tricyclo[3.3.1.03,7]nonane-3-carboxylic acid
Yield 129.1%DOI: 10.6084/m9.figshare.5104873.v1
NC12CC3CC1CC(N1CCCC1=O)(C3)C2
Reaction #1102707
1-(3-aminotricyclo[3.3.1.03,7]non-1-yl) pyrrolidin-2-one
Yield 74.0%DOI: 10.6084/m9.figshare.5104873.v1
N#C[C@@H]1CCCN1C(=O)CNC12CC3CC1CC(N1CCCC1=O)(C3)C2
Reaction #1102746
(2S)-1-{N-[2-(2-oxopyrrolidin-1-yl)hexahydro-2,5-methanopentalen-3a(1H)-yl]glycyl}pyrrolidine-2-carbonitrile
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1
N#C[C@@H]1CCCN1C(=O)CNC12CC3CC1CC(N1CCCC1=O)(C3)C2
Reaction #1102747
(2S)-1-{N-[2-(2-oxopyrrolidin-1-yl)hexahydro-2,5-methanopentalen-3a(1H)-yl]glycyl}pyrrolidine-2-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#C[C@@H]1CCCN1C(=O)CNC12CC3CC1CC(c1ccccc1)(C3)C2
Reaction #1102752
(2S)-1-[N-(2-phenylhexahydro-2,5-methanopentalen-3a(1H)-yl)glycyl]pyrrolidine-2-carbonitrile
Yield 217.5%DOI: 10.6084/m9.figshare.5104873.v1
C1CCCC(N2CCCC2)CCC1
Reaction #1254220
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[N+]1(C2CCCCCCC2)CCCC1.[I-]
Reaction #1254221
N-butyl-N-cyclooctylpyrrolidinium iodide
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[N+]1(C2CCCCCCC2)CCCC1.[OH-]
Reaction #1254222
N-butyl-N-cyclooctylpyrrolidinium hydroxide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1C12CC3CC(C1)C(C(=O)O)(C3)C2
Reaction #1305888
DOI: 10.1039/C8SC04228D
C1CCCC(N2CCCC2)CCC1
Reaction #1350563
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[N+]1(C2CCCCCCC2)CCCC1.[I-]
Reaction #1350564
N-butyl-N-cyclooctylpyrrolidinium iodide
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[N+]1(C2CCCCCCC2)CCCC1.[OH-]
Reaction #1350565
N-butyl-N-cyclooctylpyrrolidinium hydroxide
DOI: 10.6084/m9.figshare.5104873.v1
C1CCCC(N2CCCC2)CCC1
Reaction #1354997
desired product
DOI: 10.6084/m9.figshare.5104873.v1
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