部分構造検索

4176

Cl.NC[C@H]1O[C@H](c2ccccc2Cl)c2cc(Cl)ccc2N(Cc2ccccc2)C1=O
Reaction #1877
[trans-1-benzyl-7-chloro-5-(2-chlorophenyl)-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-yl]methylamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccc2c(c1)C(=O)c1ccccc1CO2
Reaction #1924
2-tert-butoxycarbonylamino-6,11-dihydrodibenz[b,e]oxepin-11-one
収率 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1(C(F)(F)F)CCN(Cc2ccccc2)C1
Reaction #1983
title compound
収率 96.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C2CC2)c2c(C)c(C3(NC(=O)OC(C)(C)C)CC3)c(F)cn2c1=O
Reaction #1996
1-cyclopropyl-8-(1-Bocamino-1-cyclopropyl)-7-fluoro-9-methyl-4-oxo-4H-quinolizine-3-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(C)(C)NC(=O)OCc1ccccc1
Reaction #1999
product
収率 75.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CC(N)(C(=O)OCc2ccccc2)C1
Reaction #6044
desired compound
収率 68.5%DOI: 10.6084/m9.figshare.5104873.v1
CCC1CCN(C(=O)C(CCCNC(=O)OCc2ccccc2)NS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1
Reaction #6464
3d
収率 91.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(CCCCNC(=O)OCc2ccccc2)C(=O)N2CCCCC2)cc1
Reaction #6466
title compound
収率 100.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCC#Cc1ccccc1
Reaction #6819
(4-phenyl-but-3-ynyl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CCc2ncc(NC(=O)OCc3ccccc3)c(=O)n21
Reaction #11051
benzyl carbamate
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c3cc(N)c4c(c3c2c1)C(=O)NC4=O
Reaction #11110
4-amino-9-methoxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
収率 93.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCCC1c1cc(NC(=O)OC(C)(C)C)ccc1OCc1ccccc1
Reaction #41543
t-butyl (3-(1-acetyl-pyrrolidin-2-yl)-4-benzyloxy-phenyl)-carbamate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c2c(CNC(=O)OC(C)(C)C)ncc(NC(=O)N(C)C)c2c1
Reaction #42924
urea
収率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(Cl)c(NC(=O)OC(C)(C)C)cc1F
Reaction #43407
1,1-Dimethylethyl [2-chloro-5-fluoro-6-(methyloxy)-3-pyridinyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccc2oc(C(=O)Nc3ccc(Cl)cn3)c(NC(=O)[C@H]3CC[C@H](N4CCOCC4=O)CC3)c2n1
Reaction #44960
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](c1ccccc1)N1C[C@@](C)(NC(=O)OC(C)(C)C)CC1=O
Reaction #45908
compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c2c(c(NC(=O)OC(C)(C)C)n(CC(=O)OC(C)(C)C)c1=O)CCN(Cc1ccc(F)c(Cl)c1)C2=O
Reaction #46284
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1nc2c(s1)C[C@@H](NC(=O)OC(C)C)CC2
Reaction #46961
isopropyl (S)-(2-acetylamino-4,5,6,7-tetrahydro-benzothiazol-6-yl)-carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C(F)(F)F)C[C@H](N=[N+]=[N-])c2cc(Br)ccc2O1
Reaction #48334
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #49214
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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