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4018

CCNC(=O)Nc1nc2nc(NCCCCN(CC)CC)ncc2cc1-c1c(Cl)cccc1Cl
Reaction #3579
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #73090
methyl and ethyl esters
DOI: 10.6084/m9.figshare.5104873.v1
COCO[C@@H]1Cc2ccccc2[C@H]1N(COC)C(=O)OC(C)(C)C
Reaction #92711
tert-butyl [(1R,2R)-2-(methoxymethoxy)-2,3-dihydro-1H-inden-1-yl](methoxymethyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(n1)c(=O)c(C(=O)c1ccc(C)c(C)c1)cn2Cc1cccc(Br)n1
Reaction #314164
1-(6-Bromo-pyridin-2-ylmethyl)-3-(3,4-dimethyl-benzoyl)-6-methyl-1H-[1,5]naphthyridin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(Cc2cccc(Br)n2)c2nc(C)ccc2c1=O
Reaction #314168
1-(6-Bromo-pyridin-2-ylmethyl)-7-methyl-4-oxo-1,4-dihydro-[1,8]naphthyridine-3-carboxylic acid ethyl ester
Выход 14.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)c2cn(Cc3cccc(Br)n3)c3cccnc3c2=O)cc1C
Reaction #314184
1-(6-Bromo-pyridin-2-ylmethyl)-3-(4-methoxy-3-methyl-benzoyl)-1H-[1,5]naphthyridin-4-one
Выход 16.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)c2cn(Cc3cccc(C)n3)c3cccnc3c2=O)cc1C
Reaction #314185
3-(4-Methoxy-3-methyl-benzoyl)-1-(6-methyl-pyridin-2-ylmethyl)-1H-[1,5]naphthyridin-4-one
Выход 37.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)c2cn(Cc3cccc(NC(=O)C(F)(F)F)n3)c3ccccc3c2=O)cc1C
Reaction #314189
2,2,2-Trifluoro-N-{6-[3-(4-methoxy-3-methyl-benzoyl)-4-oxo-4H-quinolin-1-ylmethyl]-pyridin-2-yl}-acetamide
Выход 173.9%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #414429
carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)Cc1c(Cc2ccc(Cl)cc2)c2ccc(OCc3ccc4ccccc4n3)cc2n1S(=O)(=O)c1ccccc1
Reaction #414432
title product
DOI: 10.6084/m9.figshare.5104873.v1
CO/C=C/c1nc(Br)[nH]c1C(=O)OC
Reaction #436379
Methyl 2-bromo-5-(trans-2-methoxy-vinyl)-3H-imidazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(CCCCOC1CCCCO1)CCCc1cccnc1
Reaction #552774
ethyl 3-[3-(3-pyridyl)propyl]-7-(2-tetrahydropyranyloxy)-hept-2-enoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)c1cc2ccccc2n1C(=O)OC(C)(C)C
Reaction #555611
tert-butyl 2-(1-ethoxy-1-oxopropan-2-yl)-1H-indole-1-carboxylate
Выход 89.1%DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C/[C@H]1CC[C@H](NC(=O)OC(C)(C)C)CC1
Reaction #587260
t-butyl trans-4-[(E)-1-butenyl]cyclohexyl-carbamate
Выход 39.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC/C=C/[C@H]1CC[C@@H](NC(=O)OC(C)(C)C)CC1
Reaction #587261
t-butyl cis-{4-[(E)-1-pentenyl]cyclohexyl}carbamate
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/CC[C@H]1CC[C@H](NC(=O)OC(C)(C)C)CC1
Reaction #587264
t-butyl trans-4-[(E)-3-pentenyl]cyclohexylcarbamate
Выход 9.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)c1cc2ccccc2n1C(=O)OC(C)(C)C
Reaction #590608
tert-butyl 2-(1-ethoxy-1-oxopropan-2-yl)-1H-indole-1-carboxylate
Выход 89.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)CCC[C@H]1CC[C@@H]2[C@@H](/C=C/CCOc3ccccc3)[C@H](OC3CCCCO3)C[C@@H]2OC1
Reaction #660714
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1CCOCC1
Reaction #663265
4-(prop-2-en-1-yl)tetrahydro-2 H-pyran
Выход 63.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC[C@H]1C[C@H](Oc2nc(Cl)nc3c2c(I)cn3COCC[Si](C)(C)C)C1
Reaction #664892
title compound
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
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