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2632

COc1cccc2c1cc(C)n2Cc1cccc2ccccc12
Reaction #3454
4-methoxy-2-methyl-1-[(1-naphthalenyl)methyl]-1H-indole
Выход 97.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(=O)c1ccccc1)NC1CCN(Cc2cccc3ccccc23)CC1
Reaction #3982
1-Benzoyl-3-[1-(naphth-1-ylmethyl)piperid-4-yl]urea
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCC#N)(Cc1cccc2ccccc12)C(=O)OCC
Reaction #4684
2-cyanoethyl-α-naphthylmethylmalonic acid diethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(NCCCSc1ccncc1)c1cccc2ccccc12
Reaction #6198
desired compound
Выход 74.8%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(CCl)c2ccccc12
Reaction #8301
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CCc1ccc(F)c2ccccc12
Reaction #8308
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.c1ccc([C@H]2NC(SCc3cccc4ccccc34)=N[C@H]2c2ccccc2)cc1
Reaction #47043
product 213
Выход 19.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2ccccc2c1CSC1=N[C@@H](c2ccccc2)[C@@H](c2ccccc2)N1.Cl
Reaction #47055
product 226
Выход 65.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.c1ccc([C@H]2NC(SCc3c4ccccc4cc4ccccc34)=N[C@H]2c2ccccc2)cc1
Reaction #47061
product 232
Выход 47.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc2c(cc1NC(=O)c1cccc3ccccc13)OCO2
Reaction #66926
150
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2cccc3ccccc23)CCCC12CCN(c1cnc3ccccc3n1)CC2
Reaction #69818
title compound
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NC(=O)c2cccc3ccccc23)sc1C(=O)NCc1ccccc1
Reaction #73625
title compound
Выход 12.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccccc1CCc1cccc2ccccc12
Reaction #75563
2-(2-Naphthalen-1-yl-ethyl)-benzonitrile
Выход 95.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccc2ccccc12)c1c[nH]c2ccccc12
Reaction #84199
3-(1-naphthoyl)-1H-Indole
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]cc(C(=O)c3cccc4ccccc34)c2c1
Reaction #84202
5-methoxy-3-(1-naphthoyl)-1H-indole
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(Br)c2ccccc12
Reaction #159002
4-bromonaphthalene-1-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=CC(=O)c1ccc(Br)c2ccccc12
Reaction #159003
1-(4-bromonaphthalen-1-yl)-2-diazoethanone
DOI: 10.6084/m9.figshare.5104873.v1
COCCn1c(C)c(C)s/c1=N\C(=O)c1ccc2c3c(cccc13)CC2
Reaction #165627
title compound
Выход 22.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(Br)c2ccccc12
Reaction #166954
4-bromonaphthalene-1-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=CC(=O)c1ccc(Br)c2ccccc12
Reaction #166955
1-(4-bromonaphthalen-1-yl)-2-diazoethanone
DOI: 10.6084/m9.figshare.5104873.v1
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