Background:
The most frequently used chiral auxiliaries, oxazolidinones (Evans' oxazolidinones)
have been employed in 1,4-congugate addition reactions to α,β-unsaturated carbonyl compounds. Supplementary
to our previous reports in this mini-review, we attempted to underscore the applications of this strategy in
a step (steps) in the total synthesis of some naturally occurring compounds exhibiting diverse biological activities.
Objective:
In this mini-review, we try to underscore the applications of oxazolidinones (Evans’ oxazolidinones)
in 1,4-congugate addition reactions to α,β-unsaturated carbonyl in the total synthesis of some naturally
occurring compounds exhibiting diverse biological activities.
Conclusion:
In spite of well-known superiority of asymmetric catalyzed reactions, the use of auxiliarycontrolled
reactions are still considered as commanding, vital and sometimes as only tools in the generation of
stereogenic centers during the construction of complex molecules and total synthesis of naturally occurring
compounds. The commercial availability, or readily accessibility of a wide variety of chiral amino alcohols as
starting materials to synthesize a wide range of oxazolidinones is the merits of them. In addition, the ease of
removal and subjection to various and diverse stereoselective reactions make oxazolidinones as the ideal and
superior chiral auxiliaries. In this regard, they were successfully used in asymmetric 1,4-conjugate addition reactions
with high stereoselectivities. The high degree of asymmetric induction can be attributed to the rigid
chelation of N-acyloxazolidinones with metal ions, as well as the covering of one face of the system by the
bulkiness of 4-substituent. In summary, in this report, the importance of the applications of chiral oxazolidinones
as suitable chiral auxiliaries in the stereoselective, 1,4-conjugate addition reactions in asymmetric synthesis
and in particular, the total synthesis of naturally occurring compounds and some complex molecules
were underscored. Noticeably, in these total syntheses, this chiral auxiliary is controlling the stereochemistry of
a newly created stereogenic center as well as preserving the configuration of other chiral centers, which already
have been presented in the precursor. General methods have been established for the attachment of the chiral
auxiliary as a moiety to the substrate molecule in high to excellent yields. At the end of these reactions, this
auxiliary can be easily removed leaving various desired reactive motifs for the next step in multi-step synthesis.
Hemisynthesis and Biological Evaluation of Cinnamylated, Benzylated, and Prenylated Dihydrochalcones from a Common Bio-Sourced Precursor