trimethyltin chloride

Cc1cc[c]([Sn]([CH3])([CH3])[CH3])cc1
Reaction #64374
p-tolyltrimethyltin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1cc[c]([Sn]([CH3])([CH3])[CH3])cc1
Reaction #64462
p-tolyltrimethyltin
المردود 82.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1nc[c]([Sn]([CH3])([CH3])[CH3])s1
Reaction #68541
2-methyl-5-(trimethylstannyl)thiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cn1cccc1-c1cccc(C=O)c1
Reaction #76329
3-(1-methyl-1H-pyrrol-2-yl)benzaldehyde
المردود 40.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cn1cccc1-c1cccc(C=O)c1
Reaction #78761
3-(1-methyl-1H-pyrrol-2-yl)benzaldehyde
المردود 40.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1ccc2s[c]([Sn]([CH3])([CH3])[CH3])cc2c1
Reaction #82104
5-methyl-2-trimethylstannylbenzo[b]thiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(C)(C=[CH][Sn]([CH3])([CH3])[CH3])c1ccc(Cl)cc1
Reaction #82549
3-methyl-3-(4-chlorophenyl)-1-trimethylstannyl-1-butene
المردود 87.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1n[c]([Sn]([CH3])([CH3])[CH3])cn1CC(C)(C)O[Si](C)(C)C(C)(C)C
Reaction #180701
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[CH3][Sn]([CH3])([CH3])[c]1ccccn1
Reaction #189375
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[CH3][Sn]([CH3])([CH3])[c]1cncnc1
Reaction #194829
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[CH3][Sn]([CH3])([CH3])[c]1cccnc1
Reaction #201198
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCN(CCC)C1CCc2ccc[c]([Sn]([CH3])([CH3])[CH3])c2C1
Reaction #217112
desired product
المردود 152.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
[CH3][Sn]([CH3])([CH3])[c]1ccc(Br)cc1
Reaction #232287
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(C)cc(-c2ccc3[c]([Sn]([CH3])([CH3])[CH3])c4ccccc4nc3c2)c1
Reaction #237641
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCc1cc[c]([Sn]([CH3])([CH3])[CH3])s1
Reaction #241469
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C[SiH](C)OC(c1ccc2c(c1)oc1c[c]([Sn]([CH3])([CH3])[CH3])ccc12)C(C)(C)C
Reaction #287520
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
[CH3][Sn]([CH3])([CH3])[c]1ccc(Cl)cc1
Reaction #290257
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1nc[c]([Sn]([CH3])([CH3])[CH3])s1
Reaction #306338
2-methyl-5-(trimethylstannyl)thiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
—
Reaction #344435
25.4
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
Cc1cc[c]([Sn]([CH3])([CH3])[CH3])cc1
Reaction #344734
p-tolyltrimethyltin
المردود 82.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
الصفحة 1التالي