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1649

CC(C)(C)[Si](C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2638
title compound
Выход 69.2%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCOc1c(C#N)ccc(C(Br)C(=O)O)c1OCOCCOC
Reaction #2672
[4-cyano-2,3-bis-[(2-methoxy-ethoxy)-methoxy]-phenyl]bromoacetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CCCC2(C)C(C(C)CC(Cl)CBr)=CCC12
Reaction #6379
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)N1CCN(c2cccc3c2OCCO3)CC1
Reaction #9832
IV
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(Br)C(=O)c1cnc(NC(=O)C(C)(C)C)cn1
Reaction #40277
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C(=O)c1cccc(F)c1)c1cccc(F)c1
Reaction #46988
product 20
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@H](CCBr)CCc1ccccc1
Reaction #52062
(S)-3-(t-butyldimethylsilyloxy)-5-bromo-1-phenyl pentane
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2cc(Br)ccc2c1
Reaction #59834
aimed compound
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ccc2cc(Br)ccc2c1
Reaction #59836
aimed compound
Выход 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CON=C(CBr)c1ccc(F)cc1
Reaction #61627
2-bromo-1-(4-fluorophenyl)ethanone O-methyloxime
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCOCC(COCc1cccc(CBr)c1)OC
Reaction #64229
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCOCC(COCc1cccc(CBr)c1)OC
Reaction #64230
1-(bromomethyl)-3-[[3-(hexadecyloxy)-2-methoxypropoxy]methyl]benzene
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(OC(F)F)cccc1[N+](=O)[O-]
Reaction #67498
2-difluoromethoxy-6-nitrobenzonitrile
Выход 84.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(CCO)ccc2N1
Reaction #72583
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(O)c2c1ccn(Cc1cc3ccccc3nc1Br)c2=O
Reaction #75638
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CSc1c(F)cc(CBr)cc1F
Reaction #75925
5-(bromomethyl)-1,3-difluoro-2-(methylthio)benzene
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C#N)cc(-c2ccc3c(c2)C(C)(C)OC(=O)N3)c1
Reaction #78991
3-(4,4-dimethyl-2-oxo-1,4-dihydro-2H-benzo[d][1,3]oxazin-6-yl)-5-methoxy-benzonitrile
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)N1CCN(c2cccc3c2OCCO3)CC1
Reaction #79483
IV
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(C)C)n1ccc(Br)cc1=O
Reaction #84932
Ethyl 2-(4-bromo-2-oxopyridin-1(2H)-yl)-3-methylbutanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C(=O)OCC)n1ccc(I)cc1=O
Reaction #84935
Ethyl 2-(4-iodo-2-oxopyridin-1(2H)-yl)hexanoate
DOI: 10.6084/m9.figshare.5104873.v1
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