A16171 Benzyl phenyl sulfide, 98%

Benzyl phenyl sulfide, 98%

Chemische Eigenschaften

Literaturverweise

Yong Hyeon Yim; Kwan Kim; Myung Soo Kim. Adsorption and decomposition of benzyl phenyl sulfide on silver surface investigated by Raman spectroscopy. J. Phys. Chem. 1990, 94, (6),2552-2556

Inhyung Lee; Sang Woo Han; Chang Hwan Kim; Taeg Gyum Kim; Sang Woo Joo; Du-Jeon Jang; Kwan Kim. Surface-induced photoreaction of benzyl phenyl sulfide monolayers on silver and its application to preparing patterned binary monolayers. Langmuir. 2000, 16, (26),9963-9967

Has been used in a sequence for the introduction of an ortho-substituent into aromatic amines by base-induced rearrangement of an amino sulfonium salt: J. Am. Chem. Soc., 100, 7600 (1978):

Lithiation of phenylthioethers, (t-BuLi/HMPA) leads exclusively to the ɑ-lithio derivatives, which react with electrophiles such as alkyl halides and carbonyl compounds: Tetrahedron Lett., 1961 (1977).