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363105

CCCCCCC[CH2][Sn]([Cl])([Cl])[Cl]
Reaction #54449
n-octyltin trichloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC[CH2][Sn]([Cl])([Cl])[Cl]
Reaction #54450
n-octyltin trichloride
DOI: 10.6084/m9.figshare.5104873.v1
[Cl][Sn]([CH]1CCCCC1)([CH]1CCCCC1)[CH]1CCCCC1
Reaction #74893
tricyclohexyltin chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCC[CH2][Sn]([Cl])([CH2]CCC)[CH2]c1ccccc1
Reaction #157906
benzyldibutyltin chloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(-c2ccccc2)cc1NCC1CCCN(C)C1
Reaction #160334
3-[(1-Methyl-piperidin-3-ylmethyl)-amino]-5-phenyl-thiophene-2-carboxylic acid methyl ester
Ausbeute 68.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(Br)cc1NC1CCC2(CC1)OCCO2
Reaction #160339
5-Bromo-3-(1,4-dioxa-spiro[4.5]dec-8-ylamino)-thiophene-2-carboxylic acid methyl ester
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(-c2ccccc2)cc1NC1CCC2(CC1)OCCO2
Reaction #160360
3-(1,4-Dioxa-spiro[4.5]dec-8-ylamino)-5-phenyl-thiophene-2-carboxylic acid methyl ester
Ausbeute 77.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(-c2ccccc2)cc1NC1CCSCC1
Reaction #160387
5-phenyl-3-(tetrahydro-thiopyran-4-ylamino)-thiophene-2-carboxylic acid methyl ester
Ausbeute 56.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sccc1NC1CCN(C(=O)OCc2ccccc2)CC1
Reaction #160390
4-(2-methoxycarbonyl-thiophen-3-ylamino)-piperidine-1-carboxylic acid benzyl ester
Ausbeute 101.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NCC=Cc2ccc(C(=O)Nc3ccccc3NC(=O)OC(C)(C)C)cc2)cc1OC1CCCC1
Reaction #175552
DOI: 10.1039/C8SC04228D
O=C(c1cnccc1Oc1cc(Cl)ccc1Cl)N1CCN(CC2CC2)c2ccccc21
Reaction #188414
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(CN2c3ccccc3C=Cc3ccccc32)cc1
Reaction #195630
DOI: 10.1039/C8SC04228D
COC(=O)c1sc(C2=CCCCC2)cc1NC1CCN2C(=O)CCC2C1
Reaction #199372
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc2c(c1)CCN2Cc1cc(OC)c(OC)c(OC)c1
Reaction #209280
DOI: 10.1039/C8SC04228D
COC(=O)c1sc(C#CC(C)(C)C)cc1NC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #221185
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)c1ccc(N2CCC(N3CCOCC3)C2)cc1
Reaction #228635
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc2c(CNc3ccc(N4CCOCC4)cc3)c[nH]c2c1
Reaction #242209
DOI: 10.1039/C8SC04228D
COC(=O)c1sc(C#CC(C)(C)C)cc1NC1CCC(n2ccnn2)CC1
Reaction #264620
DOI: 10.1039/C8SC04228D
CCC[CH2][Sn](=[O])[CH2]CCC
Reaction #265499
DOI: 10.1039/C8SC04228D
Cc1cccc2cc(CNc3ccc4nccnc4c3)c(-c3ccccc3)nc12
Reaction #267989
DOI: 10.1039/C8SC04228D
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