Sterically Demanding Unsymmetrical Diaryl‐λ 3 ‐iodanes for Electrophilic Pentafluorophenylation and an Approach to α‐Pentafluorophenyl Carbonyl Compounds with an All‐Carbon Stereocenter | Zendy

Matsuzaki Kohei | Zendy; Okuyama Kenta | Zendy; Tokunaga Etsuko | Zendy; Shiro Motoo | Zendy; Shibata Norio | Zendy

Open Access

Sterically Demanding Unsymmetrical Diaryl‐λ 3 ‐iodanes for Electrophilic Pentafluorophenylation and an Approach to α‐Pentafluorophenyl Carbonyl Compounds with an All‐Carbon Stereocenter

Author(s) -

Matsuzaki Kohei,

Okuyama Kenta,

Tokunaga Etsuko,

Shiro Motoo,

Shibata Norio

Publication year - 2014

Publication title -

chemistryopen

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.644

H-Index - 29

ISSN - 2191-1363

DOI - 10.1002/open.201402098

Subject(s) - halogen , electrophile , stereocenter , fluorine , steric effects , chemistry , reagent , iodine , cover (algebra) , organic chemistry , catalysis , engineering , enantioselective synthesis , mechanical engineering , alkyl

Invited for this months cover is the group of Professor Norio Shibata. The cover picture shows the Japanese painting “Genshi‐Chi” (“Primitive Land”) by Mami Shibata: our state‐of‐the‐art reagent for pentafluorophenylation is realized by the cooperation of the halogens fluorine and iodine—elements from the primitive Earth. For more details, see the Communication on 10.1002/open.201402045/full (( p. 233 ff.))

The content you want is available to Zendy users.

Already have an account? Click here to sign in.

Having issues? You can contact us here

Accelerating Research