The final step is the rearrangement to the bicyclic photoproduct.

One demonstration of this principle is found in the two bicyclic compounds depicted below.

In practice, this means that the bicyclic semigroup can be found in many different contexts.

It is a bicyclic sesquiterpene and an isomer of guaiazulene.

With bicyclic products, the cis isomer was selected for to varying degrees.

This is based on the fact that the compound is bicyclic and therefore does not adhere to the equation given above.

This radical attacks the carbonyl group to an intermediate bicyclic ketyl.

Therefore the product of the reaction is not a bicyclic structure (see tropinone and pseudopelletierine) but a 4-piperidone.

Norbornadiene is a bicyclic, hydrocarbon and an organic compound.

It is classified as a bicyclic diterpene alcohol.

There are at least three standard ways of constructing the bicyclic semigroup, and various notations for referring to it.

Both pathways include a bicyclic intermediate (4).

A bicyclic molecule is a molecule that features two fused rings.

Bicyclic molecules occur widely in organic and inorganic compounds.

His doctoral thesis was devoted to the terpenoid bicyclic hydrocarbon bornylen.

The reaction mechanism involves a bicyclic intermediate.

With very strong oxidants, S can be oxidized, for example, to give bicyclic S.

This enzyme is also called bicyclic monoterpenol dehydrogenase.

This bicyclic compound consists of the fusion of benzene and imidazole.

In mathematics, the bicyclic semigroup is an algebraic object important for the structure theory of semigroups.

An intramolecular reaction has been applied to the synthesis of novel bicyclic lactams:

The bicyclic monoid is not compact.

Cycloaddition of O gives the bicyclic peroxide.

A large number of fused bicyclic derivatives of diaryl-pyrazole and imidazoles have been reported.

Sabinene is a natural bicyclic monoterpene with the molecular formula CH.