Literature DB >> 33393310

Asymmetric Intramolecular Buchner Reaction: From High Stereoselectivity to Coexistence of Norcaradiene, Cycloheptatriene, and an Intermediate Form in the Solid State.

Benjamin Darses1,2, Pascale Maldivi3, Christian Philouze1, Philippe Dauban2, Jean-François Poisson1.   

Abstract

Bicyclic compounds bearing a quaternary stereogenic center have been obtained using asymmetric intramolecular Buchner reaction with excellent yields and level of enantioselectivity. X-ray crystallography determination of the absolute configuration of one product has led to the serendipitous observation of an unusual behavior within the crystal structure, with equilibrating norcaradiene and cycloheptatriene valence isomers at the solid state, as well as an even more unexpected intermediate form. DFT calculations were performed to support these observations.

Entities:  

Year:  2021        PMID: 33393310     DOI: 10.1021/acs.orglett.0c03774

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

Review 1.  Uncommon carbene insertion reactions.

Authors:  Ming-Yao Huang; Shou-Fei Zhu
Journal:  Chem Sci       Date:  2021-11-02       Impact factor: 9.825

2.  Enantioselective one-carbon expansion of aromatic rings by simultaneous formation and chromoselective irradiation of a transient coloured enolate.

Authors:  Rakesh K Saunthwal; James Mortimer; Andrew J Orr-Ewing; Jonathan Clayden
Journal:  Chem Sci       Date:  2022-01-25       Impact factor: 9.825

  2 in total

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