-
components of the
Staudinger ligation.
Phosphazenes are
analogues of
iminophosphoranes with the
formula (R2N)3P=NR' Zhu, Lizhao; Kinjo, Rei (2023). "Reactions...
- have the
formula R−N=P(−NR2)3.
These phosphazenes are also
known as
iminophosphoranes and
phosphine imides. They are superbases. Well
known phosphazene...
-
reaction of an
organic azide with a
phosphine or
phosphite produces an
iminophosphorane. The
reaction was
discovered by and
named after Hermann Staudinger...
-
carbenoids (produced from
diazocarbonyl compounds). The
reaction of
iminophosphoranes and
organic azides in an Aza-Wittig-reaction.
Condensation of carbon...
- Gabriele; Stölben,
Stephan (1995-01-01), Katritzky, Alan R. (ed.),
Iminophosphoranes:
Versatile Tools in
Heterocyclic Synthesis,
Advances in Heterocyclic...
-
iminophosphorane (Figure 2). This reaction,
commonly referred to as the
Staudinger reaction,
typically produces a high
yield of the
iminophosphorane....
- Guanglong; Farley,
Alistair J. M.; Dixon,
Darren J. (2020). "Bifunctional
Iminophosphorane Superbase Catalysis:
Applications in
Organic Synthesis".
Accounts of...
-
Probably the most
famous is the
reaction with phosphines,
which leads to
iminophosphoranes 22;
these can be
hydrolysed into
primary amines 23 (the Staudinger...
-
phosphine imide (sometimes
abbreviated to phosphinimide) also
known as a
iminophosphorane is a
functional group with the
formula R3P=NR.
While structurally related...
-
organic azide is not
available to
generate the
iminophosphorane. Thus, it is used to make
iminophosphoranes from
alkyl amines. Eguchi, Shoji; Matsu****a...
