-
Periodinanes also
known as λ5-iodanes are
organoiodine compounds with
iodine in the +5
oxidation state.
These compounds are
described as
hypervalent because...
- Dess–Martin
periodinane (DMP) is a
chemical reagent used in the Dess–Martin oxidation,
oxidizing primary alcohols to
aldehydes and
secondary alcohols...
- Dess–Martin
periodinane. It is
named after the
American chemists Daniel Benjamin Dess and
James Cullen Martin who
developed the
periodinane reagent in...
-
Organofluorine compounds Organochlorine compounds Organobromine compounds Iodanes Periodinanes Alex G. Fallis,
Pierre E. Tessier, "2-Iodoxybenzoic acid (IBX)1" Encyclopedia...
- or a Cr(VI) compound.
Milder conditions make use of the Dess–Martin
periodinane or the Moffatt–Swern methods. Many
other methods have been developed...
-
secondary alcohols to ketones.
These include Collins reagent and Dess-Martin
periodinane. The
direct oxidation of
primary alcohols to
carboxylic acids can be...
-
October 2017.
Boeckman Jr RK, Shao P,
Mullins JJ (2000). "Dess–Martin
periodinane: 1,1,1-Triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one" (PDF). Organic...
- oxidations, and
hypervalent iodine compounds, such as the Dess–Martin
periodinane. One
disadvantage to the use of PCC is its toxicity,
which it shares...
- the
hypervalent organoiodine compounds (i.e., IBX acid, Dess–Martin
periodinane),
although these often also
oxidize the α position. A Lux-Flood acid...
-
bidentate ligand and a
tridentate analog, co-invented the Dess–Martin
periodinane,
creator of the
Martin sulfurane Emil
Wolfgang Menzel Jr. (Ph.D. 1958)...
