Substructure Search

4937

CCCCc1nc(I)c(CO)[nH]1
Reaction #2441
crystals
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N=c1sc(I)cn1-c1cccc(C(F)(F)F)c1
Reaction #5412
2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-iodothiazoline
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ncnc2[nH]cc(I)c12
Reaction #10256
title compound
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1oc2c(I)c(O)ccc2c(=O)c1-c1ccc(Cl)cc1
Reaction #42774
3-(4-Chlorophenyl)-7-hydroxy-8-iodo-2-isopropyl-chromen-4-one
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(I)c2scc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #45397
desired product
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(I)c2scc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #45418
desired product
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2coc3c(I)cnc(N)c23)ccc1NC(=O)OC(C)(C)C
Reaction #45469
title compound
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(I)c2onc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #45523
title compound
Yield 64.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(C(=O)O)c(C)c(I)c1Br
Reaction #45541
compound
Yield 57.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(C(=O)O)c(C)c(I)c1F
Reaction #45567
compound
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(I)c(C)c(Br)c1F
Reaction #45579
4-Bromo-3-fluoro-6-iodo-2-methoxy-5-methylphenylamine
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@H]1CCN(c2c(-c3ccccc3)cc(C#N)c(N)c2I)C1
Reaction #45813
compound
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](OCc1ccccc1)[C@@H](COC(CI)OCCC(C)(C)C)NC(=O)OC(C)(C)C
Reaction #48614
title compound
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCCI)[C@@H](CO[Si](C)(C)C(C)(C)C)NC(=O)OC(C)(C)C
Reaction #48617
desired compound
Yield 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](COCc1ccccc1)COC(CI)(c1ccccc1)c1ccccc1
Reaction #48672
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)COC(OCCI)[C@H](COCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #48683
desired compound
Yield 84.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@]1(O)C[C@H]2CN(CCc3c([nH]c4c(I)cccc34)[C@@](C(=O)OC)(c3cc4c(cc3OC)N(C)[C@H]3[C@@](O)(C(=O)OC)[C@H](OC(C)=O)[C@]5(CC)C=CCN6CC[C@]43[C@@H]65)C2)C1
Reaction #48763
12′-iodovinblastine
Yield 112.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)Nc1nc(O)c2c(C#C[Si](C)(C)C)c[nH]c2n1
Reaction #50299
N-[4-hydroxy-5-(trimethylsilyl) ethynyl-7H-pyrrolo [2,3-d]pyrimidin-2-yl]-2,2-dimethyl propionamide
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N=c1sc(I)cn1-c1cccc(C(F)(F)F)c1
Reaction #50308
2-ethoxycarbonylimino-3-(3-tri-fluoromethylphenyl)-5-iodothiazoline
Yield 14.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(Cc2ccc(OC(F)(F)F)cc2)C(=O)N(c2cc(Cl)cc(Cl)c2)c2ncc(I)n21
Reaction #52116
(R)-1-(3,5-dichloro-phenyl)-5-iodo-3-methyl-3-(4-trifluoromethoxy-benzyl)-1H-imidazo[1,2-α]imidazol-2-one
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
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