52096-57-8Relevant academic research and scientific papers
Exocyclic-endocyclic n-acyliminium ion equilibration via an intramolecular α-thioamidoalkylation in the synthesis of fused N,S-heterocyclic systems: Some new parameters
Hucher, Nicolas,Pesquet, Anthony,Netchitailo, Pierre,Daich, Adam
, p. 2758 - 2770 (2007/10/03)
The reactivity of N-[aryl(or alkyl)thio(oxo or seleno)alkylamidals 6 bearing the N-(CH2)n-X-(CH2)m-Ar functionality towards neat TFA has been examined. Substrates of type 6 give, together with the products 11, 17, 19, and
Phthalimidomethyl Group. A New Protecting Group of Thiols
Gong, Young-Dae,Iwasawa, Nobuharu
, p. 2139 - 2142 (2007/10/02)
Phthalimidomethyl group is employed as a protecting group of thiols.This group can be introduced to thiols under mild reaction conditions and be removed by treatment with hydrazine hydrate followed by mercuric acetate or cupric acetate.
Photochemistry of the Phthalimide System, 37. - Thiazacycloalkanols by Photocyclization of S-Substituted N-(Thioalkyl)phthalimides
Sato, Yasuhiko,Nakai, Hideo,Wada, Masao,Mizoguchi, Tomishige,Hatanaka, Yasumaru,et al.
, p. 1099 - 1118 (2007/10/02)
N-Substituted phthalimides (1,2) possessing a terminal thioether function in their side chain were irradiated with a high-pressure mercury lamp to give a variety of thiazacycloalkanol derivatives (3,7,9-13,16,17) with favored γ-, δ-, ε-, and ζ-hydrogen abstractions (Table 1), in moderate to fairly good yields.
