Substructure Search

COc1cc(C)ccn1

CN(C)CCOc1nc2ccccc2c2c1C(=O)c1cc3c(cc1-2)OCO3
Reaction #3255
title compound
Yield 68.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COc2cc(/C=C/c3ccc(F)cc3)ccn2)cc1
Reaction #43328
title compound
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(/C=C/c2ccc(F)cc2)ccn1-c1ccc(OCCN2CCCC2)cc1
Reaction #43329
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)CCc1cc(CO[Si](C)(C)C(C)(C)C)cc(OC)n1
Reaction #43627
desired product
Yield 99.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CO[Si](C)(C)C(C)(C)C)cc(CCCO)n1
Reaction #43628
product
Yield 102.3%DOI: 10.6084/m9.figshare.5104873.v1
COCc1c(OC)nc(C(C)C)c(/C=C/C=O)c1-c1ccc(F)cc1
Reaction #65196
(E)-3-[4-(4-Fluorophenyl)-6-isopropyl-2-methoxy-3-methoxymethyl-pyridin-5-yl]-prop-2-enal
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(=O)CC(O)/C=C/C1=C(C(C)C)N(C)C(OC)C(OC)=C1c1ccc(F)cc1
Reaction #65197
Methyl (E)-7-[4-(4-fluorophenyl)-6-isopropyl-2-methoxy-3-methoxy-methyl-pyridin-5-yl]-5-hydroxy-3-oxo-hept-6-enoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(Cl)n1
Reaction #66132
2-chloro-6-methoxy-4-methyl-pyridine
Yield 63.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)O)c2cccc(F)c2n1
Reaction #75710
8-Fluoro-2-methoxyquinoline-4-carboxylic Acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cnc(Cl)c3ccccc23)ccn1
Reaction #77502
1-chloro-4-[2-(2-methoxy-pyridin-4-yl)-ethyl]-isoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cccc(-c2cc(OC)nc3ccc(C(O)(c4cccnc4)c4cccnc4)cc23)c1
Reaction #78454
37A
Yield 41.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cccc(-c2cc(=O)[nH]c3ccc(C(O)(c4cccnc4)c4cccnc4)cc23)c1
Reaction #78455
title compound
Yield 44.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccnc(SCCCC(=O)NC/C=C\COc2cc(CN3CCCCC3)ccn2)n1
Reaction #80355
title compound
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccnc1SCCCC(=O)NC/C=C\COc1cc(CN2CCCCC2)ccn1
Reaction #80356
title compound
Yield 49.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(SCCCC(=O)NC/C=C\COc2cc(CN3CCCCC3)ccn2)o1
Reaction #80357
title compound
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(SCCCC(=O)NC/C=C\COc2cc(CN3CCCCC3)ccn2)s1
Reaction #80359
title compound
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(Cl)nc(OCc2ccsc2)c1
Reaction #83409
2-chloro-6-(3-thienylmethyloxy)-4-trifluoromethylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cccc(Oc2cc(C(F)(F)F)cc(OCc3ccsc3)n2)c1
Reaction #83410
2-(3-thienylmethyloxy)-4-trifluoromethyl-6-(meta-trifluoromethylphenoxy)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cc(Cl)ccc2C#C[Si](C)(C)C)ccn1
Reaction #84915
4-{5-Chloro-2-[(trimethylsilyl)ethynyl]phenyl}-2-methoxypyridine
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)C#Cc1ccc(Cl)cc1-c1cc[nH]c(=O)c1
Reaction #84916
4-{5-Chloro-2-[(trimethylsilyl)ethynyl]phenyl}pyridin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
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