Literature DB >> 26646367

Catalytic asymmetric formal γ-allylation of deconjugated butenolides.

Amit K Simlandy1, Santanu Mukherjee1.   

Abstract

A formal γ-allylation of deconjugated butenolides is reported based on a two-step sequence consisting of a catalytic diastereo- and enantioselective vinylogous nucleophilic addition to vinyl sulfones and Julia-Kocienski olefination. This highly modular approach delivers densely functionalized butenolides containing a quaternary stereogenic centre in excellent yield with high enantioselectivity.

Entities:  

Year:  2016        PMID: 26646367     DOI: 10.1039/c5ob02362a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

1.  Diastereoselective Organocatalytic Addition of α-Angelica Lactone to β-Halo-α-ketoesters.

Authors:  Jessica A Griswold; Matthew A Horwitz; Leslie V Leiva; Jeffrey S Johnson
Journal:  J Org Chem       Date:  2017-02-06       Impact factor: 4.354

2.  Iridium-catalyzed enantioselective direct vinylogous allylic alkylation of coumarins.

Authors:  Rahul Sarkar; Sankash Mitra; Santanu Mukherjee
Journal:  Chem Sci       Date:  2018-06-04       Impact factor: 9.825

Review 3.  Modern Synthetic Strategies with Organoselenium Reagents: A Focus on Vinyl Selenones.

Authors:  Martina Palomba; Italo Franco Coelho Dias; Ornelio Rosati; Francesca Marini
Journal:  Molecules       Date:  2021-05-25       Impact factor: 4.411

  3 in total

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