Substructure Search

C1CCC(C1)CN

CCCc1nc2cc(N(Cc3ccccc3)C(=O)C3CCCC3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43862
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(Cc3ccccc3)C(=O)C3CCCC3)ccc2n1CC(=O)O
Reaction #43863
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1C[C@@H]2CC3(C[C@@H]2C1)OCCO3
Reaction #48009
(3aR,6aS)-2-butylspiro[hexahydrocyclopenta[c]pyrrole-5(1H),2′-[1,3]dioxolane]
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1(C(=O)Nn2cccc2)CCCC1
Reaction #50661
product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CC2CCC1C2)c1ccncc1Nc1ccc(I)cc1F
Reaction #67856
N-bicyclo[2.2.1]hept-2-yl-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
C#CCC(C1CCCC1)n1cc(-c2ncnc3[nH]ccc23)cn1
Reaction #69286
product
Yield 81.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1(CO)CCCC1
Reaction #69291
product
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1(CO)CCCC1
Reaction #73323
product
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC2CC3CCC2C3)SC12CCC2
Reaction #74324
6-(Bicyclo[2.2.1]hept-2-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC2CC3CCC2C3)SC1(CCO)CCO
Reaction #74406
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OCCC1(CCOS(C)(=O)=O)SC(NC2CC3CCC2C3)=NC1=O
Reaction #74407
Methanesulfonic acid 2-[2-(bicyclo[2.2.1]hept-2-ylamino)-5-(2-methanesulfonyloxy-ethyl)-4-oxo-4,5-dihydro-thiazol-5-yl]-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC1(CC2CCN(S(C)(=O)=O)CC2)SC(N[C@H]2CC3CCC2C3)=NC1=O
Reaction #74412
title compound
Yield 42.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCCC12SC(N[C@H]1C[C@@H]3CC[C@H]1C3)=NC2=O
Reaction #74413
2-((1S,2S,4R)-bicyclo[2.2.1]hept-2-ylamino)-6,6-dimethyl-7-oxa-1-thia-3-azaspiro[4.4]non-2-en-4-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCOCCOCCOCCOCCNC(=O)CCN1C(=O)C=CC1=O)NCCC1(C(=O)N[C@@H](Cc2ccc(NC(=O)c3c(Cl)cccc3Cl)cc2)C(=O)O)CCCC1
Reaction #91998
desired product
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(O[C@@H]2C[C@@H]3CN[C@H]2C3)nc1
Reaction #92493
title compound
Yield 112.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CC2CCC1C2)c1ccncc1Nc1ccc(I)cc1F
Reaction #166021
N-bicyclo[2.2.1]hept-2-yl-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(O)CC1C(=O)NC1(C#N)CC1
Reaction #174085
DOI: 10.1039/C8SC04228D
CC(C)(C)NC(=O)C1CCC2C3CCC4=CC(=O)CCC4(C)C3CCC12C
Reaction #179831
DOI: 10.1039/C8SC04228D
O=Cc1c[nH]c2cc(C(=O)NCC3CCCC3)ccc12
Reaction #182451
DOI: 10.1039/C8SC04228D
O=P(O)(O)O
Reaction #193156
DOI: 10.1039/C8SC04228D
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