4.6 Article

Asymmetric Conjugate Additions and Allylic Alkylations Using Nucleophiles Generated by Hydro- or Carbometallation

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 21, Issue 15, Pages 5668-5678

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201405855

Keywords

asymmetric catalysis; conjugate addition; metallation reactions; Michael addition; synthetic methods

Funding

  1. EPSRC [EP/H003711/1]
  2. EPSRC [EP/H003711/1] Funding Source: UKRI
  3. Engineering and Physical Sciences Research Council [EP/H003711/1] Funding Source: researchfish

Ask authors/readers for more resources

This Minireview discusses catalytic asymmetric conjugate addition and allylic alkylation reactions where the nucleophiles were generated in situ by hydrometallation or carbometallation. This exciting recent trend in asymmetric catalysis promises to expand the range of transformations available for the rapid and selective assembly of complex, functional molecules for both academic and industrial research. This Minireview aims to serve as a reference for studies reported to date and discusses the current state-of-theart, scope and limitations of these processes.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available