部分構造検索

CC(C)OC(=O)C

COc1ccc(CCCCCCCCOc2ccc(CO)nc2C=CC(=O)OC(C)(C)C)cc1
Reaction #1848
t-Butyl 3-{6-hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoate
DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(C)(C)c2cccc(N)c21
Reaction #2465
desired product
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@H](n2c(Cl)nc3cc(Cl)c(Cl)cc32)[C@H](O)[C@@H]1O
Reaction #6441
2,5,6-Trichloro-1-(β-D-ribofuranosyl)benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #6879
material
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CN2C(=O)c3ccccc3C2=O)cc1
Reaction #53133
4-phthalimidomethyl-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)/C=C/c1ccc(O)c(O)c1
Reaction #56616
caffeic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=C(CCl)CN(Cc1ccccc1)[C@@H](CC(=O)OC(C)(C)C)C(=O)OCc1ccccc1
Reaction #89694
(2S)-[benzyl-(2-chloromethyl-allyl)-amino]-succinic acid 1-benzyl ester 4-tert-butyl ester
収率 58.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC(N)Cc1ccc(-c2ccccc2)cc1.Cl
Reaction #158015
3-amino-4-biphenyl-4-yl-butyric acid tert-butyl ester hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)CCC(=O)O
Reaction #158042
(R)-4-(1-(biphenyl-4-yl)-4-tert-butoxy-4-oxobutan-2-ylamino)-4-oxobutanoic acid
収率 36.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC(Cc1ccc(-c2ccccc2)cc1)NC(=O)OC(C)(C)C
Reaction #158066
tert-butyl 4-(biphenyl-4-yl)-3-(tert-butoxycarbonylamino)butanoate
収率 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)O[C@H]1CN2CCC1CC2
Reaction #164153
(S)-((R)-quinuclidin-3-yl) 2-(tert-butoxycarbonylamino)-3-phenylpropanoate
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@H]1CN2CCC1CC2)C(Nc1cccc(OC(F)(F)F)c1)c1ccccc1
Reaction #164166
title compound
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(NC(C(=O)O[C@H]2CN3CCC2CC3)c2ccccc2)c1
Reaction #164168
title compound
収率 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(c1ccccc1)C(C(=O)O[C@H]1CN2CCC1CC2)c1ccccc1
Reaction #164187
title compound
収率 38.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@H]1CN2CCC1CC2)C(Nc1cccc(F)c1)c1ccc(F)cc1
Reaction #164193
title compound
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C(Nc2ccccc2)C(=O)O[C@H]2CN3CCC2CC3)cc1
Reaction #164201
desired compound
収率 21.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cncn1C1c2ccccc2C(=O)OC1(C)C
Reaction #177099
DOI: 10.1039/C8SC04228D
CC1(C)OC(=O)c2ccccc2C1n1cncc1CN
Reaction #185533
DOI: 10.1039/C8SC04228D
CCC=Cc1cncn1C1c2ccccc2C(=O)OC1(C)C
Reaction #192391
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #196274
DOI: 10.1039/C8SC04228D
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