子结构搜索

CCC#Cc1ccccn1

CCC#Cc1ccccn1

收率 84.3%DOI: 10.6084/m9.figshare.5104873.v1

CCC#Cc1cccc[n+]1N.Cc1cc(C)c(S(=O)(=O)[O-])c(C)c1

N-amino-2-(1-butynyl)pyridinium mesitylenesulfonate

收率 39.1%DOI: 10.6084/m9.figshare.5104873.v1

CCC#Cc1cc(OC)ccn1

2-(1-butynyl)-4-methoxypyridine

DOI: 10.6084/m9.figshare.5104873.v1

DOI: 10.6084/m9.figshare.5104873.v1

CCc1cc2c(OC)cccn2n1

收率 66.5%DOI: 10.6084/m9.figshare.5104873.v1

C[C@@H](Nc1nc(OC2CC2)c2nc(C#CC3CC3)ccc2n1)c1ccc(S(N)(=O)=O)cc1

Reaction #70645

desired product

收率 77.7%DOI: 10.6084/m9.figshare.5104873.v1

O=C(Nc1ccc(C#CCCN2CC=C(c3ccccc3)CC2)nc1)c1cccs1

Reaction #81925

DOI: 10.6084/m9.figshare.5104873.v1

CC(C)=CCCC(C)CCOc1ccc(C#Cc2ccc(C(=O)O)cc2)nc1CCC(=O)O

Reaction #83549

DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)CCC#Cc1ccc(O)c(CCC(=O)OC)n1

Reaction #83588

5-[3-hydroxy-2-(2-methoxycarbonylethyl)-6-pyridyl]-4-pentynoic acid methyl ester

收率 84.3%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)CCCCc1ccc(O)c(CCC(=O)OC)n1

Reaction #83589

5-[3-hydroxy-2-(2-methoxycarbonylethyl)-6-pyridyl]-pentanoic acid methyl ester

收率 65.6%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)CCc1nc(C#CCCCO)ccc1O

Reaction #83591

3-[3-hydroxy-6-(5-hydroxy-1-pentynyl)-2-pyridyl]-propionic acid methyl ester

收率 28.0%DOI: 10.6084/m9.figshare.5104873.v1

C(#Cc1ccccn1)CCNc1nc2ccccc2s1

Reaction #174004

DOI: 10.1039/C8SC04228D

COc1ccc(C2(C#Cc3ccccn3)CCC(=O)CC2)cc1OC1CCCC1

Reaction #177310

DOI: 10.1039/C8SC04228D

CNCCC#Cc1cccc(CF)n1

Reaction #183414

DOI: 10.1039/C8SC04228D

CCOC(=O)C(C)(C)Oc1ccc(OCCCC#Cc2ccc(C(F)(F)F)cn2)cc1C

Reaction #185008

DOI: 10.1039/C8SC04228D

N#Cc1ccc(CCC#Cc2ccccn2)cc1

Reaction #187805

DOI: 10.1039/C8SC04228D

CCC#Cc1cccc[n+]1N

Reaction #189342

DOI: 10.1039/C8SC04228D

CC(O)C=Cc1ccc(Br)cn1

Reaction #190012

DOI: 10.1039/C8SC04228D

CC(C)(O)C#Cc1cccc(Nc2sc(-c3c(F)cc(C(C)(C)O)cc3F)cc2C(N)=O)n1

Reaction #194474

DOI: 10.1039/C8SC04228D

CS(=O)(=O)OCCC#Cc1cccc(CF)n1

Reaction #194496

DOI: 10.1039/C8SC04228D

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