Busqueda de Subestructura

C1CSC=C1

O=C(c1cccc(C(=O)C2(Cl)CC=CS2)c1)C1(Cl)CC=CS1
Reaction #65610
1,3-Bis(2-chlorothiophenoyl)Benzene
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1sc(C(=O)O)c2c1OCCO2
Reaction #75461
2,5-dicarboxy-3,4-ethylenedioxythiophene
DOI: 10.6084/m9.figshare.5104873.v1
O=S1CCC2=C1C=NC(Cl)N2NC1(CO)CC1
Reaction #157275
[1-(2-chloro-5-oxo-6,7-dihydro-5H-5λ4-thieno[3,2-d]pyrimidin-1-ylamino)-cyclopropyl]-methanol
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)C1=CC2SC=CC2S1
Reaction #159173
title compound
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C1=CC2SC=CC2S1
Reaction #159174
title compound
Rendimiento 124.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)C1=CC2SC=CC2S1
Reaction #159175
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1C(=O)OCC(=O)C1=CC2SC=CC2S1
Reaction #159176
title compound
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1C(=O)OCC(=O)C1=CC2SC(Br)=CC2S1
Reaction #159177
title compound
Rendimiento 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CCCC1c1ncc(C2=CC3SC(Br)=CC3S2)[nH]1)C(C)C
Reaction #159178
title compound
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CCCC1c1ncc(C#CC2=CC3SC(c4cnc(C5CCCN5C(=O)C(NC(=O)OC)C(C)C)[nH]4)=CC3S2)[nH]1)C(C)C
Reaction #159179
title compound
Rendimiento 18.0%DOI: 10.6084/m9.figshare.5104873.v1
COOCNC(C(=O)N1CCCC1c1ncc(-c2ccc(C3=CC4SC(c5cnc(C6CCCN6C(=O)C(NC(=O)OC)C(C)C)[nH]5)=CC4S3)cc2)[nH]1)c1ccccc1
Reaction #159181
title compound
Rendimiento 63.8%DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)C1=CC2SC=CC2S1
Reaction #167116
title compound
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C1=CC2SC=CC2S1
Reaction #167117
title compound
Rendimiento 124.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)C1=CC2SC=CC2S1
Reaction #167118
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1C(=O)OCC(=O)C1=CC2SC=CC2S1
Reaction #167119
title compound
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1C(=O)OCC(=O)C1=CC2SC(Br)=CC2S1
Reaction #167120
title compound
Rendimiento 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CCCC1c1ncc(C2=CC3SC(Br)=CC3S2)[nH]1)C(C)C
Reaction #167121
title compound
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CCCC1c1ncc(C#CC2=CC3SC(c4cnc(C5CCCN5C(=O)C(NC(=O)OC)C(C)C)[nH]4)=CC3S2)[nH]1)C(C)C
Reaction #167122
title compound
Rendimiento 18.0%DOI: 10.6084/m9.figshare.5104873.v1
COOCNC(C(=O)N1CCCC1c1ncc(-c2ccc(C3=CC4SC(c5cnc(C6CCCN6C(=O)C(NC(=O)OC)C(C)C)[nH]5)=CC4S3)cc2)[nH]1)c1ccccc1
Reaction #167124
title compound
Rendimiento 63.8%DOI: 10.6084/m9.figshare.5104873.v1
O=S1(=O)CCC(NCCO)C1
Reaction #172894
desired product
DOI: 10.6084/m9.figshare.5104873.v1
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