子结构搜索

1108540

$CO/N=C(\C(=O)Cl)c1nsc(N)n1$

Reaction #50750

2-(5-amino-1,2,4-thiadiazol-3-yl)-2(Z]-methoxyiminoacetyl chloride

DOI: 10.6084/m9.figshare.5104873.v1

$CO/N=C(\C(=O)Cl)c1nsc(N)n1$

Reaction #50751

2-(5-amino-1,2,4-thiadiazol-3-yl)-2(Z)-methoxyiminoacetyl chloride

DOI: 10.6084/m9.figshare.5104873.v1

$CO/N=C(\C(=O)Cl)c1nsc(N)n1$

Reaction #50752

DOI: 10.6084/m9.figshare.5104873.v1

$CO/N=C(\C(=O)Cl)c1nsc(N)n1$

Reaction #50753

2-(5-amino-1,2,4-thiadiazol-3-yl)-2(Z)-methoxyiminoacetyl chloride

DOI: 10.6084/m9.figshare.5104873.v1

$CO/N=C(\C(=O)Cl)c1nsc(N)n1$

Reaction #50754

2-(5-amino-1,2,4-thiadiazol-3-yl)-2(Z)-methoxyiminoacetyl chloride

DOI: 10.6084/m9.figshare.5104873.v1

Nc1nc(/C(=N/OCF)C(=O)Cl)ns1

Reaction #50755

DOI: 10.6084/m9.figshare.5104873.v1

Nc1nc(/C(=N/OCF)C(=O)Cl)ns1

Reaction #50756

2-(5-amino-1,2,4-thiadiazol-3-yl)-2(Z)-fluoromethoxyiminoacetyl chloride

DOI: 10.6084/m9.figshare.5104873.v1

Cl.Nc1nc(C(=NOCF)C(=O)Cl)ns1

Reaction #50757

收率 106.0%DOI: 10.6084/m9.figshare.5104873.v1

$CO/N=C(\C(=O)Cl)c1nsc(N)n1$

Reaction #50758

2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(Z)-methoxyiminoacetyl chloride

DOI: 10.6084/m9.figshare.5104873.v1

O=S(=O)(CCCCl)NOCc1ccccc1

Reaction #65155

N-benzyloxy-3-chloropropylsulfonamide

收率 41.0%DOI: 10.6084/m9.figshare.5104873.v1

COc1cc(-c2nocc2-c2cccnc2C(F)(F)F)cc([N+](=O)[O-])c1OC

Reaction #70930

3-(3,4-dimethoxy-5-nitrophenyl)-4-(2-(trifluoromethyl)pyridin-3-yl)isoxazole

DOI: 10.6084/m9.figshare.5104873.v1

$O=C(NC/C(=N\OCC1CC1)c1ncc(C(F)(F)F)cc1Cl)c1ccccc1C(F)(F)F$

Reaction #84273

desired product

收率 94.7%DOI: 10.6084/m9.figshare.5104873.v1

O=C(NC/C(=N/OCC1CC1)c1ncc(C(F)(F)F)cc1Cl)c1ccccc1C(F)(F)F

Reaction #84274

desired product

收率 55.3%DOI: 10.6084/m9.figshare.5104873.v1

CCON=C(CN1C(=O)c2ccccc2C1=O)c1ncc(C(F)(F)F)cc1Cl

Reaction #84279

desired product

收率 46.4%DOI: 10.6084/m9.figshare.5104873.v1

CCON=C(CN)c1ncc(C(F)(F)F)cc1Cl

Reaction #84280

desired product

收率 61.9%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)O/N=C(/CNC(=O)c1ccccc1C(F)(F)F)c1ncc(C(F)(F)F)cc1Cl

Reaction #84332

desired product

收率 51.2%DOI: 10.6084/m9.figshare.5104873.v1

COc1cc(-c2nocc2-c2cccnc2C(F)(F)F)cc([N+](=O)[O-])c1OC

Reaction #90275

3-(3,4-dimethoxy-5-nitrophenyl)-4-(2-(trifluoromethyl)pyridin-3-yl)isoxazole

DOI: 10.6084/m9.figshare.5104873.v1

O=C(c1ccc(C2=NOC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)C2)cc1C(F)(F)F)N1CC(=O)N(CC(F)(F)F)C(=O)C1

Reaction #92126

4-([4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydro-1,2-oxazol-3-yl]-2-(trifluoromethyl)phenyl]carbonyl)-1-(2,2,2-trifluoroethyl)piperazine-2,6-dione

DOI: 10.6084/m9.figshare.5104873.v1

O=C1CN(C(=O)c2ccc(C3=NOC(c4cc(Cl)cc(C(F)(F)F)c4)(C(F)(F)F)C3)cc2C(F)(F)F)CC(=O)N1

Reaction #92131

4-[(4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-4,5-dihydro-1,2-oxazol-3-yl]-2-(trifluoromethyl)phenyl)carbonyl]piperazine-2,6-dione

DOI: 10.6084/m9.figshare.5104873.v1

CCCN1C(=O)CN(C(=O)c2ccc(C3=NOC(c4cc(Cl)cc(C(F)(F)F)c4)(C(F)(F)F)C3)cc2C(F)(F)F)CC1=O

Reaction #92132

4-[(4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-4,5-dihydro-1,2-oxazol-3-yl]-2-(trifluoromethyl)phenyl)carbonyl]-1-propylpiperazine-2,6-dione

DOI: 10.6084/m9.figshare.5104873.v1

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