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249641

CC(C)C1SC(NC2CC3CCC2C3)=NC1=O
Reaction #74314
2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CCC1SC(NC2CC3CCC2C3)=NC1=O
Reaction #74315
2-(bicyclo[2.2.1]hept-2-ylamino)-5-ethyl-1,3-thiazol-4(5H)-one
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)SC1Cc1ccc(O)cc1
Reaction #74335
2-(bicyclo[2.2.1]hept-2-ylamino)-5-(4-hydroxybenzyl)-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC2CC3CCC2C3)SC12CCCCC2
Reaction #74348
2-(Bicyclo[2.2.1]hept-2-ylamino)-1-thia-3-azaspiro[4.5]dec-2-en-4-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(N[C@H]2C[C@@H]3CC[C@H]2C3)SC12CCOCC2
Reaction #74400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(N[C@H]2C[C@@H]3CC[C@H]2C3)SC1CCOC1CCCCO1
Reaction #74401
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)CC1(CCOC2CCCCO2)SC(N[C@H]2C[C@@H]3CC[C@H]2C3)=NC1=O
Reaction #74402
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)CC1(CCO)SC(N[C@H]2C[C@@H]3CC[C@H]2C3)=NC1=O
Reaction #74403
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC2(CCO1)SC(N[C@H]1C[C@@H]3CC[C@H]1C3)=NC2=O
Reaction #74404
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #74405
solid
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
O=C1N=C(NC2CC3CCC2C3)SC12CCN(C1CCCC1)CC2
Reaction #74408
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(CC2CCNCC2)SC(N[C@H]2CC3CCC2C3)=NC1=O
Reaction #74409
title compound
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCOc1cccc(C(=O)N2CCC(CC3(C)SC(N[C@H]4CC5CCC4C5)=NC3=O)CC2)c1
Reaction #74410
title compound
Ausbeute 412.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCC(CC2(C)SC(N[C@H]3CC4CCC3C4)=NC2=O)CC1
Reaction #74411
title compound
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
Ausbeute 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
—
Reaction #74414
solid
DOI: 10.6084/m9.figshare.5104873.v1
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