tributyltin chloride

CCc1cc(OCc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)c2ccccc2n1.Cl

2-ethyl-4-[(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methoxy]-quinoline hydrochloride

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1scnc1C1OCCO1

収率 98.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cnccc1NC(=O)OC(C)(C)C

(3-tributylstannyl-pyridin-4-yl)-carbamic acid tert-butyl ester

収率 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cc(C)c(C2OCCO2)s1

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1c(F)cncc1F

Reaction #40513

3,5-Difluoro-4-tributylstannanyl-pyridine

収率 89.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ncco1

Reaction #49226

2-(tributylstannyl)oxazole

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ccoc1

Reaction #50187

(3-furanyl)tributylstannane

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1c(I)ncn1C

Reaction #60883

収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1nnn(COCc2ccccc2)n1

Reaction #70822

2-(benzyloxymethyl)-5-(tributylstannyl)-2H-tetrazole

収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1scnc1C1OCCO1

Reaction #79380

収率 98.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ccc(Cl)s1

Reaction #80920

(5-chlorothien-2-yl)tributyl tin

収率 98.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04

CCC[CH2][SnH]([CH2]CCC)[CH2]CCC.Clc1ccc(Cl)nn1

Reaction #82703

3,6-dichloropyridazine tributylstannane

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04

$CCC[CH2][Sn](/[CH]=C\CO)([CH2]CCC)[CH2]CCC$

Reaction #87947

(Z)-3-tributylstannanyl-prop-2-en-1-ol

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)/[C](=C/[C@H]1CCC(=O)N1Cc1ccc(OC)cc1OC)c1ccc(C(C)(C)C)cc1

Reaction #157726

収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cc2cc3s[c]([Sn]([CH2]CCC)([CH2]CCC)[CH2]CCC)cc3cc2s1

Reaction #159212

2,6-bis(tri-n-butylstannyl)-benzo[1,2-b:4,5-b′]dithiophene

収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cc2cc3s[c]([Sn]([CH2]CCC)([CH2]CCC)[CH2]CCC)cc3cc2s1

Reaction #167154

2,6-bis(tri-n-butylstannyl)-benzo[1,2-b:4,5-b′]dithiophene

収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09

CSc1nc(N)nc(C2=CCCCO2)c1C#N

Reaction #176524

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCC[CH2][Sn]([C]#CCCOC1CCCCO1)([CH2]CCC)[CH2]CCC

Reaction #176854

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCC[CH2][Sn]([C]#CC#CC(C)(C)C)([CH2]CCC)[CH2]CCC

Reaction #178534

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1nc(Cl)c2ncn(C3OC(CO[Si](C)(C)C(C)(C)C)C4OC(C)(C)OC43)c2n1

Reaction #179876

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

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