Site-, enantio- and stereo-selectivities of the 1,3-dipolar cycloaddition reactions of oxanorbornadiene with C,N-disubstituted nitrones and dimethyl nitrilimines: a DFT mechanistic study-Reference-Cited by-同舟云学术

Site-, enantio- and stereo-selectivities of the 1,3-dipolar cycloaddition reactions of oxanorbornadiene with C,N-disubstituted nitrones and dimethyl nitrilimines: a DFT mechanistic study

Published:2020-01 Issue:1 Volume:139 Page:
ISSN:1432-881X
Container-title:Theoretical Chemistry Accounts
language:en
Short-container-title:Theor Chem Acc

Author:

Opoku Ernest,Arhin Grace,Pipim George Baffour,Adams Anita Houston,Tia Richard^ORCID,Adei Evans

Funder

National Council for Tertiary Education

Publisher

Springer Science and Business Media LLC

Subject

Physical and Theoretical Chemistry

Link

http://link.springer.com/content/pdf/10.1007/s00214-019-2529-8.pdf

Reference33 articles.

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3. Hashimoto T, Maruoka K (2015) Recent advances of catalytic asymmetric 1,3-dipolar cycloadditions. Chem Rev 115:5366–5412. https://doi.org/10.1021/cr5007182

4. Alcaide B, Almendros P, Alonso JM, Aly MF, Pardo C, Sáez E, Torres MR (2002) Efficient entry to highly functionalized β-lactams by regio- and stereoselective 1,3-dipolar cycloaddition reaction of 2-azetidinone-tethered nitrones. J Org Chem 67:7004–7013. https://doi.org/10.1021/jo025924e

5. Cheviet T, Dujardin G, Parrot I, Martinez J, Mousseron M, De Montpellier U, Bataillon PE (2016) Isoxazolidine: a privileged scaffold for organic and medicinal chemistry. Chem Rev. https://doi.org/10.1021/acs.chemrev.6b00543

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