Synthesis, Structure, and Thermolysis of Tris(dimethylphenylsilyl)methyl Sulfenyl Chloride

2017 ◽  
Vol 46 (6) ◽  
pp. 837-839
Author(s):  
Koh Sugamata ◽  
Shigeru Ishii
Keyword(s):  
2011 ◽  
Vol 47 (25) ◽  
pp. 7095 ◽  
Author(s):  
Abdelaziz Houmam ◽  
Hamida Muhammad ◽  
M'hamed Chahma ◽  
Kallum Koczkur ◽  
Daniel F. Thomas

1976 ◽  
Vol 54 (3) ◽  
pp. 498-499 ◽  
Author(s):  
Richard F. Langler

Benzylic sulfides have been shown to furnish sulfonyl chlorides in excellent yields, upon reaction with molecular chlorine in aqueous acetic acid. The reaction most likely proceeds through the intermediacy of the corresponding sulfenyl chloride.


Author(s):  
G. Graner ◽  
E. Hirota ◽  
T. Iijima ◽  
K. Kuchitsu ◽  
D. A. Ramsay ◽  
...  
Keyword(s):  

1971 ◽  
Vol 2 (42) ◽  
pp. no-no
Author(s):  
P. VINKLER ◽  
F. KLIVENYI ◽  
E. VINKLER ◽  
G. STAJER ◽  
A. E. SZABO
Keyword(s):  

1970 ◽  
Vol 48 (22) ◽  
pp. 3593-3597 ◽  
Author(s):  
J. W. Greidanus

Reduction (NaBH4) of adamantanethione gives high yields of pure 2-adamantanethiol, from which several derivatives including the methyl sulfide, sulfoxide, and sulfone were prepared. The sulfenyl chloride was prepared and used insitu. From the n.m.r. spectra the aromatic solvent-induced shifts Δ = τ(benzene) – τ(CCl4 or CDCl3) were determined, where possible.


ChemInform ◽  
2004 ◽  
Vol 35 (18) ◽  
Author(s):  
A. V. Borisov ◽  
G. N. Borisova ◽  
Yu. A. Nikonova ◽  
V. K. Osmanov ◽  
Zh. V. Matsulevich
Keyword(s):  

1972 ◽  
Vol 8 (4) ◽  
pp. 468-472 ◽  
Author(s):  
L. S. Sologub ◽  
S. D. Moshchitskii ◽  
Ya. N. Ivashchenko ◽  
Yu. N. Levchuk
Keyword(s):  

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