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ICI

CCCCCCCC[C@H]1C[C@H]1CCCCCCCC(=O)O
Reaction #5364
cis-8-(2 -octylcyclopropyl) octanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C1OC(n2cnc3c(Cl)nc(I)nc32)C(OC(=O)c2ccccc2)C1OC(=O)c1ccccc1
Reaction #10554
title compound
Выход 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](n2cnc3c(Cl)nc(I)nc32)[C@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #44331
[(2R,3R,4R,5R)-3,4-diacetyloxy-5-(6-chloro-2-iodopurin-9-yl)oxolan-2-yl]methyl acetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CI)CCCC1
Reaction #44866
title compound
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(C(F)(F)F)ccc1I
Reaction #45324
2-Iodo-5-(trifluoromethyl)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
OCc1cc(I)cc(C(F)(F)F)c1
Reaction #45335
[3-iodo-5-(trifluoromethyl)phenyl]methanol
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCOc2c(I)cccc21
Reaction #51263
4,4-dimethyl-8-iodochroman
DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC1c1cccc(C2(c3ccc(OC(F)F)cc3)N=C(N)N(C)C2=O)c1
Reaction #58864
title compound
Выход 16.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(I)ncc1[N+](=O)[O-]
Reaction #62343
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(Cl)c(I)c(OC)c1
Reaction #69518
title compound
Выход 66.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c[nH]nc1I
Reaction #70549
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C(C)=O)C1(c2ccccc2)CC1
Reaction #73508
methyl 3-oxo-2(1-phenylcyclopropyl)butanoate
Выход 26.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C[C@@H](C)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O)C[C@H]3C[C@@]312
Reaction #77687
(7α,14β,15β,17β)-3-methoxy-7-methyl-14,15-methyleneestra-1,3,5(10)-trien-17-ol
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(C=CI)c1ccc(Cl)cc1
Reaction #82530
1,1-difluoro-1-(4-chlorophenyl)-3-iodo-2-propene
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C=CI)c1ccc(Cl)cc1
Reaction #82532
1-oxo-1-(4-chlorophenyl)-3-iodo-2-propene
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(OCn2ccc3ccc([N+](=O)[O-])cc32)c1
Reaction #84515
title compound
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc(C#N)c(I)n1CC(C)(C)O
Reaction #91979
title compound
Выход 57.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)OCc1ccccc1)C1CC1CCO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
Reaction #157671
title compound
Выход 513.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(COCc3ccccc3)CC2C1
Reaction #157970
tert-butyl 6-[(benzyloxy)methyl]-3-azabicyclo[4.I.0]heptane-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC2(CC2)CN1C(=O)OCc1ccccc1
Reaction #159071
5-aza-spiro[2.4]heptane-5,6-dicarboxylic acid 5-benzyl ester 6-methyl ester
Выход 65.1%DOI: 10.6084/m9.figshare.5104873.v1
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