Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
January 1, 2005Chemical Communications

Enantioselective construction of stereogenic quaternary centres via Rh-catalyzed asymmetric addition of alkenylboronic acids to α,β-unsaturated pyridylsulfones

View Full Paper
Ask AI
Bookmark
Share

Authors

PMPablo MauleónUniversidad Autónoma de MadridJCJuan C. CarreteroInstitute of Advanced Chemistry of Catalonia

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Mauleón et al. (2005) studied this question.

synapsesocial.com/papers/6a85adeffc70cb81dc203b03https://doi.org/10.1039/b508142d
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Rhodium-Catalyzed Enantioselective Conjugate Addition of Organoboronic Acids to α,β-Unsaturated Sulfones2004 · 115 citations
  2. 2Recent Advances in Catalytic Enantioselective Michael Additions2001 · 950 citations
  3. 3Rhodium-Catalyzed Conjugate Addition of Aryl- or 1-Alkenylboronic Acids to Enones1997 · 559 citations
  4. 4Enantioselective Synthesis of Nitroalkanes Bearing All-Carbon Quaternary Stereogenic Centers through Cu-Catalyzed Asymmetric Conjugate Additions2005 · 152 citations
  5. 5Enantioselective Synthesis of Quaternary Stereocenters via a Catalytic Asymmetric Stetter Reaction2004 · 322 citations