部分構造検索

1718

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
COc1ccc(CCCCCCCCOc2ccc(CO)nc2C=CC(=O)O)cc1
Reaction #1849
3-{6-Hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C(=O)OCCCC)c1nc(CO)ccc1OCc1ccccc1
Reaction #1853
n-Butyl (3-benzyloxy-6-hydroxymethylpyridin-2-yl)propenoate
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C(=O)OC)c1nc(CO)ccc1OCc1ccccc1
Reaction #1854
product
収率 84.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1nc(-c2ccncc2)cs1
Reaction #4448
1-phenyl-1-[4-(4-pyridyl)-2-thiazolyl]methanone
収率 18.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC[C@H](COCc2ccccc2)O1
Reaction #8294
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(-c2nn3c(c2-c2ccc(F)cc2)CC[C@H]3CC#N)n1
Reaction #8375
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CCc2ncc(N(Cc3cccc(C(F)(F)F)c3)C(=O)OCc3ccccc3)c(=O)n21
Reaction #11082
3-(trifluoromethyl)benzyl amine
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CSCc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11788
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C)[N+](=O)[O-]
Reaction #11793
title compound
収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNC1CCCCC1
Reaction #40626
title compound
収率 72.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CCc1ccc2c(c1OCc1ccccc1)CCCC2
Reaction #42195
2-allyl-5,6,7,8-tetrahydronaphthalen-1-yl benzyl ether
収率 88.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CCc1cc(OC)c2c(c1OCc1ccccc1)[C@H]1CC[C@@H]2C1
Reaction #42211
(1R*,4S*)-6-allyl-5-(benzyloxy)-8-methoxy-1,2,3,4-tetrahydro-1,4-methanonaphthalene
収率 90.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCc1cc2n(c(=O)c1)CCC2
Reaction #43629
desired product
収率 84.9%DOI: 10.6084/m9.figshare.5104873.v1
CNCCCCn1c(C(=O)OC)c2c(c(O)c1=O)C(=O)N(Cc1ccc(F)c(Cl)c1)CC2
Reaction #46271
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)[C@@H](c1ccccc1)N1CCC(C)(O)CC1)c1ccccc1
Reaction #46638
title compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)[C@@H](c1ccccc1)N1CCC(O)(c2ccccc2)CC1)c1ccccc1
Reaction #46643
title compound
収率 27.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(C#Cc2ccccc2)cc1
Reaction #47178
N-(2-Benzoyl-4-chloro-phenyl)-4-phenylethynyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2c[nH]nc2C(=O)Nc2ccc(F)cc2)CC1
Reaction #48591
solid
収率 19.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCCCOc1cc(I)c2c(c1Cl)CNC2=O
Reaction #49594
4-chloro-5-[3-(tert-butyldimethylsiloxy)propoxy]-7-iodoisoindolinone
収率 79.7%DOI: 10.6084/m9.figshare.5104873.v1
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