Visnevska et al., 2012 - Google Patents
Evaluation of (E)-2-chlorovinylsulfones as novel class of cytotoxic agents and highly (E)-stereoselective addition of N-, S-and Senucleophiles to (E)-2 …Visnevska et al., 2012
View PDF- Document ID
- 16140793021671066861
- Author
- Visnevska J
- Belyakov S
- Shestakova I
- Gulbe A
- Jaschenko E
- Abele E
- Publication year
- Publication venue
- Heterocycl. Lett
External Links
Snippet
Novel phase transfer catalytic(PTC) method for the conjugate addition-elimination of N-, S- and Se-nucleophiles to (E)-2-chlorovinylsulfones has been developed. Products were isolated in yields up to 98%.(E)-2-Chlorovinylsulfones exhibit very high cytotoxicity against …
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