部分構造検索

366678

COC(=O)c1ccc(C=O)nc1
Reaction #58729
title compound
収率 46.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #86631
compound 6
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC(I)(C(=O)OCC)C(=O)OCC
Reaction #305239
diethyl 2-allyl-2-iodomalonate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(CO)CO)c1c(I)c(C(=O)NC(CO)CO)c(I)c(N2C(=O)COCC2CO)c1I
Reaction #320250
solid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OC[C@@H](CC1(I)CC1)O[Si](C)(C)C(C)(C)C
Reaction #422808
(R)-5-((1-iodocyclopropyl)methyl)-2,2,3,3,8,8,9,9-octamethyl-4,7-dioxa-3,8-disiladecane
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H](O)CC1(I)CC1
Reaction #422809
(R)-3-(1-iodocyclopropyl)propane-1,2-diol
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC[C@@H](CC2(I)CC2)O1
Reaction #422810
(R)-4-((1-iodocyclopropyl)methyl)-2,2-dimethyl-1,3-dioxolane
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC[C@@H](CC2(S(=O)(=O)Cl)CC2)O1
Reaction #422811
(R)-1-((2,2-dimethyl-1,3-dioxolan-4-yl)methyl)cyclopropane-1-sulfonyl chloride
収率 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OC[C@H](CC1(I)CC1)O[Si](C)(C)C(C)(C)C
Reaction #422815
(S)-5-((1-iodocyclopropyl)methyl)-2,2,3,3,8,8,9,9-octamethyl-4,7-dioxa-3,8-disiladecane
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@@H](O)CC1(I)CC1
Reaction #422816
(S)-3-(1-iodocyclopropyl)propane-1,2-diol
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC[C@H](CC2(I)CC2)O1
Reaction #422817
(S)-4-((1-iodocyclopropyl)methyl)-2,2-dimethyl-1,3-dioxolane
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CC3CC1CC(I)(C3)C2
Reaction #442735
5-iodoadamantan-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1=CCC(CC(C)C)([I+]c2ccccc2)C=C1.F[P-](F)(F)(F)(F)F
Reaction #468386
p-isobutylphenyl-p-tolyl-iodonium hexafluorophosphate
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1C[C@@]2(C)[C@@H](CC[C@@H]3[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]32)C[C@]1(C)I
Reaction #630834
2β-acetyloxy-3α-iodo-3β-methyl-5α-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccnc2cc(Cl)c(Cl)cc12
Reaction #686539
compound
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(OCC2CCCC2)cc1
Reaction #716317
4-(cyclopentylmethoxy)benzaldehyde
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(C)CS[C@@H]2C(NC(=O)COc3ccccc3)C(=O)N12
Reaction #734955
methyl 7-(2-phenoxyacetamido)-3-methyl-3-cephem-4-carboxylate
収率 27.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCC(CC2(I)CC2)O1
Reaction #751684
DOI: 10.1039/C8SC04228D
CCOC(=O)c1sc(C(F)(F)F)c(C#N)c1I
Reaction #895184
DOI: 10.1039/C8SC04228D
CC(C)(C)ON1C(C)(C)CC(OC(=O)c2ccccc2)CC1(C)C
Reaction #900205
DOI: 10.1039/C8SC04228D
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