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Literature DB >> 20718062

Enantiodifferentiating endo-selective oxylactonization of ortho-alk-1-enylbenzoate with a lactate-derived aryl-λ3-iodane.

Morifumi Fujita¹, Yasushi Yoshida, Kazuyuki Miyata, Akihiro Wakisaka, Takashi Sugimura.

Abstract

Entities: Chemical

Year: 2010 PMID： 20718062 DOI： 10.1002/anie.201003503

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

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16 in total

1. Catalytic, Enantioselective 1,2-Difluorination of Cinnamamides.

Authors: Moriana K Haj; Steven M Banik; Eric N Jacobsen
Journal: Org Lett Date: 2019-04-09 Impact factor: 6.005

2. Enantioselective, Catalytic Fluorolactonization Reactions with a Nucleophilic Fluoride Source.

Authors: Eric M Woerly; Steven M Banik; Eric N Jacobsen
Journal: J Am Chem Soc Date: 2016-10-13 Impact factor: 15.419

3. Asymmetric oxidative dearomatizations promoted by hypervalent iodine(III) reagents: an opportunity for rational catalyst design?

Authors: Andrew M Harned
Journal: Tetrahedron Lett Date: 2014-08-20 Impact factor: 2.415

4. Dihydropyranone formation by ipso C-H activation in a glucal 3-carbamate-derived rhodium acyl nitrenoid.

Authors: Brisa Hurlocker; Nadia C Abascal; Lindsay M Repka; Elsy Santizo-Deleon; Abigail L Smenton; Victoria Baranov; Ritu Gupta; Sarah E Bernard; Shenjuti Chowdhury; Christian M Rojas
Journal: J Org Chem Date: 2011-03-07 Impact factor: 4.354

5. Mechanism and Origins of Chemo- and Stereoselectivities of Aryl Iodide-Catalyzed Asymmetric Difluorinations of β-Substituted Styrenes.

Authors: Biying Zhou; Moriana K Haj; Eric N Jacobsen; K N Houk; Xiao-Song Xue
Journal: J Am Chem Soc Date: 2018-11-05 Impact factor: 15.419

Enantiodifferentiating endo-selective oxylactonization of ortho-alk-1-enylbenzoate with a lactate-derived aryl-λ3-iodane.

1. Catalytic, Enantioselective 1,2-Difluorination of Cinnamamides.

2. Enantioselective, Catalytic Fluorolactonization Reactions with a Nucleophilic Fluoride Source.

3. Asymmetric oxidative dearomatizations promoted by hypervalent iodine(III) reagents: an opportunity for rational catalyst design?

4. Dihydropyranone formation by ipso C-H activation in a glucal 3-carbamate-derived rhodium acyl nitrenoid.

5. Mechanism and Origins of Chemo- and Stereoselectivities of Aryl Iodide-Catalyzed Asymmetric Difluorinations of β-Substituted Styrenes.

6. Catalytic, Diastereoselective 1,2-Difluorination of Alkenes.

7. Enantioselective diamination with novel chiral hypervalent iodine catalysts.

8. Facile oxidative rearrangements using hypervalent iodine reagents.

9. Thioamination of Alkenes with Hypervalent Iodine Reagents.

10. Enantioselective Oxidative Rearrangements with Chiral Hypervalent Iodine Reagents.