Literature DB >> 31754289

Intermolecular Stereoselective Iridium-Catalyzed Allylic Alkylation: An Evolutionary Account.

Samantha E Shockley1, J Caleb Hethcox1, Brian M Stoltz1.   

Abstract

Our lab has long been interested in the development of methods for the creation of enantioenriched all-carbon quaternary stereocenters. Historically, our interest has centered on palladium-catalyzed allylic alkylation, though recent efforts have moved to include the study of iridium catalysts. Whereas palladium catalysts enable the preparation of isolated stereocenters, the use of iridium catalysts allows for the direct construction of vicinal stereocenters via an enantio-, diastereo-, and regioselective allylic alkylation. This account details the evolution of our research program from inception, which focused on the first iridium-catalyzed allylic alkylation to prepare stereodyads containing a single quaternary center, to our most recent discovery that allows for the synthesis of vicinal quaternary centers.

Entities:  

Keywords:  allylic alkylation; asymmetric catalysis; enantioselective; iridium; quaternary stereocenters; umpolung

Year:  2018        PMID: 31754289      PMCID: PMC6870865          DOI: 10.1055/s-0037-1610217

Source DB:  PubMed          Journal:  Synlett        ISSN: 0936-5214            Impact factor:   2.454


  45 in total

1.  Very efficient phosphoramidite ligand for asymmetric iridium-catalyzed allylic alkylation.

Authors:  Alexandre Alexakis; Damien Polet
Journal:  Org Lett       Date:  2004-09-30       Impact factor: 6.005

2.  The catalytic enantioselective, protecting group-free total synthesis of (+)-dichroanone.

Authors:  Ryan M McFadden; Brian M Stoltz
Journal:  J Am Chem Soc       Date:  2006-06-21       Impact factor: 15.419

3.  Phosphoramidite ligands in iridium-catalyzed allylic substitution.

Authors:  Damien Polet; Alexandre Alexakis; Karine Tissot-Croset; Clémence Corminboeuf; Klaus Ditrich
Journal:  Chemistry       Date:  2006-04-24       Impact factor: 5.236

4.  Study of Intermediates in Iridium-(Phosphoramidite,Olefin)-Catalyzed Enantioselective Allylic Substitution.

Authors:  Simon L Rössler; Simon Krautwald; Erick M Carreira
Journal:  J Am Chem Soc       Date:  2017-03-07       Impact factor: 15.419

5.  Enantioselective synthesis of all-carbon quaternary stereogenic centers in acyclic systems.

Authors:  Jaya Prakash Das; Ilan Marek
Journal:  Chem Commun (Camb)       Date:  2011-02-28       Impact factor: 6.222

6.  Formaldehyde N,N-dialkylhydrazones as neutral formyl anion equivalents in iridium-catalyzed asymmetric allylic substitution.

Authors:  Simon Breitler; Erick M Carreira
Journal:  J Am Chem Soc       Date:  2015-04-17       Impact factor: 15.419

7.  Enantioselective Iridium-Catalyzed Allylic Alkylation Reactions of Masked Acyl Cyanide Equivalents.

Authors:  J Caleb Hethcox; Samantha E Shockley; Brian M Stoltz
Journal:  Org Lett       Date:  2017-03-14       Impact factor: 6.005

8.  Catalytic enantioselective construction of quaternary stereocenters: assembly of key building blocks for the synthesis of biologically active molecules.

Authors:  Yiyang Liu; Seo-Jung Han; Wen-Bo Liu; Brian M Stoltz
Journal:  Acc Chem Res       Date:  2015-02-25       Impact factor: 22.384

9.  Catalytic enantioselective synthesis of quaternary carbon stereocentres.

Authors:  Kyle W Quasdorf; Larry E Overman
Journal:  Nature       Date:  2014-12-11       Impact factor: 49.962

10.  Squaramide-catalyzed enantioselective Michael addition of masked acyl cyanides to substituted enones.

Authors:  Kin S Yang; Antoinette E Nibbs; Yunus E Türkmen; Viresh H Rawal
Journal:  J Am Chem Soc       Date:  2013-10-17       Impact factor: 15.419

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  2 in total

1.  Controllable, Sequential, and Stereoselective C-H Allylic Alkylation of Alkenes.

Authors:  Ling Qin; Mohammed Sharique; Uttam K Tambar
Journal:  J Am Chem Soc       Date:  2019-10-15       Impact factor: 15.419

2.  Enantioselective and Diastereodivergent Allylation of Propargylic C-H Bonds.

Authors:  Jin Zhu; Yidong Wang; Aaron D Charlack; Yi-Ming Wang
Journal:  J Am Chem Soc       Date:  2022-08-17       Impact factor: 16.383

  2 in total

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