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Pregled bibliografske jedinice broj: 1172245

Enantioselective construction of a congested quaternary stereogenic center in isoindolinones bearing three aryl groups via an organocatalytic formal Betti reaction

Beriša, Arben; Glavač, Danijel; Zheng, Chao; You, Shu-Li; Gredičak, Matija
Enantioselective construction of a congested quaternary stereogenic center in isoindolinones bearing three aryl groups via an organocatalytic formal Betti reaction // Organic Chemistry Frontiers, 9 (2022), 428-435 doi:10.1039/d1qo01684a (međunarodna recenzija, članak, znanstveni)

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Naslov
Enantioselective construction of a congested quaternary stereogenic center in isoindolinones bearing three aryl groups via an organocatalytic formal Betti reaction
(Enantioselective construction of a congested quaternary stereogenic center in isoindolinones bearing three aryl groups via an organocatalytic formal Betti reaction)

Autori
Beriša, Arben ; Glavač, Danijel ; Zheng, Chao ; You, Shu-Li ; Gredičak, Matija

Izvornik
Organic Chemistry Frontiers (2052-4110) 9 (2022); 428-435

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
three aryl groups ; Betti reaction

Sažetak
An efficient enantioselective formal Betti reaction between phenols and diaryl ketimines generated in situ from isoindolinone alcohols is described. In a reaction catalyzed by a chiral phosphoric acid, a broad range of ketimines and phenols afforded isoindolinone derivatives comprising a congested quaternary stereogenic center bearing three aryl groups in high yields, and high regioselectivities and enantioselectivities.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA

Projekti:
HRZZ-IP-2018-01-4053 - Nove strategije za pripravu tetrasupstituiranih kiralnih centara: asimetrične katalitičke reakcije usmjerene protuanionom (NSYNC-ACDC) (Gredičak, Matija, HRZZ - 2018-01) ( CroRIS)

Ustanove:
Institut "Ruđer Bošković", Zagreb

Profili:

Avatar Url Danijel Glavač (autor)

Avatar Url Arben Beriša (autor)

Avatar Url Matija Gredičak (autor)

Poveznice na cjeloviti tekst rada:

Pristup cjelovitom tekstu rada doi pubs.rsc.org doi.org

Citiraj ovu publikaciju:

Beriša, Arben; Glavač, Danijel; Zheng, Chao; You, Shu-Li; Gredičak, Matija
Enantioselective construction of a congested quaternary stereogenic center in isoindolinones bearing three aryl groups via an organocatalytic formal Betti reaction // Organic Chemistry Frontiers, 9 (2022), 428-435 doi:10.1039/d1qo01684a (međunarodna recenzija, članak, znanstveni)
Beriša, A., Glavač, D., Zheng, C., You, S. & Gredičak, M. (2022) Enantioselective construction of a congested quaternary stereogenic center in isoindolinones bearing three aryl groups via an organocatalytic formal Betti reaction. Organic Chemistry Frontiers, 9, 428-435 doi:10.1039/d1qo01684a.
@article{article, author = {Beri\v{s}a, Arben and Glava\v{c}, Danijel and Zheng, Chao and You, Shu-Li and Gredi\v{c}ak, Matija}, year = {2022}, pages = {428-435}, DOI = {10.1039/d1qo01684a}, keywords = {three aryl groups, Betti reaction}, journal = {Organic Chemistry Frontiers}, doi = {10.1039/d1qo01684a}, volume = {9}, issn = {2052-4110}, title = {Enantioselective construction of a congested quaternary stereogenic center in isoindolinones bearing three aryl groups via an organocatalytic formal Betti reaction}, keyword = {three aryl groups, Betti reaction} }
@article{article, author = {Beri\v{s}a, Arben and Glava\v{c}, Danijel and Zheng, Chao and You, Shu-Li and Gredi\v{c}ak, Matija}, year = {2022}, pages = {428-435}, DOI = {10.1039/d1qo01684a}, keywords = {three aryl groups, Betti reaction}, journal = {Organic Chemistry Frontiers}, doi = {10.1039/d1qo01684a}, volume = {9}, issn = {2052-4110}, title = {Enantioselective construction of a congested quaternary stereogenic center in isoindolinones bearing three aryl groups via an organocatalytic formal Betti reaction}, keyword = {three aryl groups, Betti reaction} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus

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