部分構造検索

c1ccc2c(c1)CCCC2

Cl.NNc1ccc(C(=O)O)c2c1CCCC2
Reaction #1178
hydrazine
収率 73.3%DOI: 10.6084/m9.figshare.5104873.v1
OC1CCCc2ccc(OCc3ccncc3)cc21
Reaction #1706
Compound 2
収率 78.2%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CNC2CCCc3ccc(OCc4ccncc4)cc32)cc1
Reaction #1707
Compound 12
収率 97.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCc2cccc(COC3CCCCO3)c21
Reaction #9355
8-(tetrahydro-pyran-2-yloxymethyl)-3,4-dihydro-2H-naphthalen-1-one
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(C)Oc1cccc2c1CCCC2
Reaction #47337
3-(5,6,7,8-tetrahydro-naphthalen-1-yloxy)-but-2-enoic acid ethyl ester
収率 72.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(CBr)Oc1cccc2c1CCCC2
Reaction #47338
4-bromo-3-(5,6,7,8-tetrahydro-naphthalen-1-yloxy)-but-2-enoic acid ethyl ester
収率 71.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC(C)C)N1CC(Oc2cccc3c2CCCC3)=CC1=O
Reaction #47339
(S)-4-methyl-2-[2-oxo-4-(5,6,7,8-tetrahydro-naphthalen-1-yloxy)-2,5-dihydro-pyrrol-1-yl]-pentanoic acid methyl ester
収率 15.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1(C)C(=O)CCc2ccc(OC)cc21
Reaction #54671
Ethyl 7-methoxy-1-methyl-2-oxo-1,2,3,4-tetrahydro-1-naphthaleneacetate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCc2cccc(COC3CCCCO3)c21
Reaction #56996
8-(tetrahydro-pyran-2-yloxymethyl)-3,4-dihydro-2H-naphthalen-1-one
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCOc1ccc2c(c1)CCCC2N
Reaction #60388
compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCOc1ccc2c(c1)CCCC2NC(=O)CC(NS(=O)(=O)c1ccc(Cl)c(Cl)c1)c1ccccc1
Reaction #60389
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC1CCCc2cc(CO)ccc21
Reaction #60390
title compound
DOI: 10.6084/m9.figshare.5104873.v1
OC1Cc2ccccc2C(c2ccccn2)C1
Reaction #74781
2-(3-Hydroxy-1,2,3,4-tetrahydronaphthalenyl)-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCCC1C1CC(O)Cc2ccccc21
Reaction #74782
2-(3-hydroxy-1,2,3,4-tetrahydronaphthalenyl)-1-methyl piperidine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCc2cc(OCCc3ccccc3)ccc21
Reaction #91363
title compound
収率 61.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCc2cc(C3=CCOCC3)ccc21
Reaction #91911
title compound
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(=O)O
Reaction #177656
DOI: 10.1039/C8SC04228D
c1ccc(NC2=NC3CCCc4cccc(c43)N2)cc1
Reaction #179930
DOI: 10.1039/C8SC04228D
Cc1cc2c(c(O)c1C=O)CCCC2
Reaction #190795
DOI: 10.1039/C8SC04228D
CN(C)CCC1CCc2cc(O)ccc2C1
Reaction #192706
DOI: 10.1039/C8SC04228D
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