部分構造検索

6989

CCOC(=O)CCCc1cccc(Br)c1
Reaction #1302
Compound D
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=CCc1ccc(Br)cc1
Reaction #1306
ethyl 4-(4-bromophenyl)but-2-enoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCc1cccc(Br)c1
Reaction #1452
Compound D
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=CCc1ccc(Br)cc1
Reaction #1461
ethyl 4-(4-bromophenyl)but-2-enoate
DOI: 10.6084/m9.figshare.5104873.v1
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)N1C(=O)[C@@H](C/C=C/C(=O)O)O[C@H](c2ccccc2Cl)c2cc(Cl)ccc21
Reaction #1883
trans-7-chloro-5-(2-chlorophenyl)-1-isopropyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-crotonic acid
収率 77.1%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
COC(=O)c1sccc1C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
Reaction #1927
2-methoxycarbonylthiophen-3-ylmethyltriphenylphosphonium bromide
収率 70.4%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
COC(=O)c1ccc(/C=C/c2cccc[c]2[Na])c(S(=O)(=O)O)c1
Reaction #2074
white powder
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2ccccc2c1-c1c(CP(=O)(c2ccccc2)c2ccccc2)ccc2ccccc12
Reaction #2493
2-diphenylphosphinylmethyl-2'-methyl-1,1'-binaphthyl
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2ccccc2c1-c1c(CP(c2ccccc2)c2ccccc2)ccc2ccccc12
Reaction #2494
2-diphenylphosphinomethyl-2'-methyl-1,1'-binaphthyl
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C/c1cc(=O)c(OCc2ccccc2)c[nH]1
Reaction #4212
title compound
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
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