- all
cycloadditions are
concerted and thus pericyclic.
Nonconcerted cycloadditions are not pericyclic. As a
class of
addition reaction,
cycloadditions permit...
-
cycloaddition is a
chemical reaction between a 1,3-dipole and a
dipolarophile to form a five-membered ring. The
earliest 1,3-dipolar
cycloadditions were...
- In
organic chemistry, enone–alkene
cycloadditions are a
version of the [2+2]
cycloaddition. This
reaction involves an
enone and
alkene as substrates....
-
intermediates in
chemical synthesis. A
nitrone is a 1,3-dipole used in
cycloadditions, and a
carbonyl mimic. Nitrones, as a
tetrasubstituted double bond,...
-
better than others:[clarification needed] [3+2]
cycloadditions, such as the ****sgen 1,3-dipolar
cycloaddition, in
particular the Cu(I)-catalyzed stepwise...
-
result of
templating by the metal. (4)
Although notable work on [6+4]
cycloadditions was
reported by
Rigby et al. in the late 1980s, the
study of metal-complexed...
- metal-catalyzed (5+2)
cycloadditions of
vinylcyclopropanes with 2π
units are also
useful for the
formation of seven-membered rings.
Cycloadditions carried out under...
- act as 4π
partners in [4+2]
cycloadditions as well. The
unique transition state geometry of [2+2]
ketene cycloadditions has
important stereochemical...
- PMID 21970470. ****sgen, Rolf. (1976). "1,3-Dipolar
cycloadditions. 76.
Concerted nature of 1,3-dipolar
cycloadditions and the
question of
diradical intermediates"...
- [2+2]
cycloadditions are only
observed under photochemical activation. The
rationale for the non-observation of
thermal [2+2]
cycloadditions begins with...
