子结构搜索

791243

CN1CCC=C(CO)C1
Reaction #40778
colorless oil
收率 98.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC=C(C=O)C1
Reaction #40779
orange oil
收率 109.7%DOI: 10.6084/m9.figshare.5104873.v1
C[NH+]1CCC=C(C(=O)O)C1.[Cl-]
Reaction #47744
product
收率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CN(Cc2ccccc2)CCC1c1ccsc1
Reaction #58542
subtitle compound
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccc(OCCO)cc2)C[C@@H]2CN(C(C)=O)C[C@H]1N2C(=O)OC(C)(C)C(Cl)(Cl)Cl
Reaction #61309
(rac.)-(1R*,5S*)-3-Acetyl-7-[4-(2-hydroxyethoxy)phenyl]-3,9-diazabicyclo-[3.3.1]non-6-ene-6,9-dicarboxylic acid 6-ethyl ester 9-(2,2,2-trichloro-1,1-dimethylethyl) ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC2CC(c3ccc(OCCOc4cc(F)ccc4Cl)cc3)=C(C(=O)O)C(C1)N2C(=O)OC(C)(C)C(Cl)(Cl)Cl
Reaction #61311
3-Acetyl-7-{4-[2-(2-chloro-5-fluorophenoxy)ethoxy]phenyl}-3,9-diazabicyclo-[3.3.1]non-6-ene-6,9-dicarboxylic acid 9-(2,2,2-trichloro-1,1-dimethylethyl) ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=CCCN(C)C1
Reaction #63429
Arecoline
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(C#CCO)CCN(Cc2ccccc2)C1
Reaction #67991
methyl 1-benzyl-4-(3-hydroxy-1-propin-1-yl)-1,2,5,6-tetrahydropyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #88350
Intermediate 47
DOI: 10.6084/m9.figshare.5104873.v1
C=C1C(=O)N(C)CCC1(CC(=O)OC)c1cccc(OC)c1
Reaction #96076
4-methoxycarbonylmethyl-4-(3'-methoxyphenyl)-1-methyl-3-methylene-2-piperidone
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@]23CCN(C)C(=O)[C@H]2CCC(=O)C3)c1
Reaction #96078
cis-1,6-Dioxo-4a-(3'-methoxyphenyl)-2-methyldecahydroisoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=CCCN(CCC2Cc3ccccc3OC2(C)C)C1
Reaction #180789
DOI: 10.1039/C8SC04228D
CC1CC(c2ccc(Cl)c(Cl)c2)=C(CO)CN1C(=O)OC(C)(C)C
Reaction #181598
DOI: 10.1039/C8SC04228D
COC(=O)C1=C(c2ccc(Cl)c(Cl)c2)CCN(C(=O)OC(C)(C)C)C1
Reaction #181670
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(c2ccccc2)=C(C(=O)O)C1
Reaction #196610
DOI: 10.1039/C8SC04228D
C=CCOC(=O)N1CC(C(=O)OC)=CCC1C
Reaction #204381
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=C(CC)CCN(C(=O)OC(C)(C)C)C1
Reaction #206838
DOI: 10.1039/C8SC04228D
COC(=O)C1=C(c2ccc(C(F)(F)F)c(Cl)c2)CCN(C(=O)OCc2ccccc2)C1
Reaction #227871
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CN(CC2=Cc3ccc(OC)cc32)CCC1OCc1ccccc1
Reaction #229569
DOI: 10.1039/C8SC04228D
CCOC(=O)CSC1=C(C(=O)OC)CN(C(=O)c2ccccc2)CC1
Reaction #235800
DOI: 10.1039/C8SC04228D
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