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Pregled bibliografske jedinice broj: 918975

Control of Enantioselectivity in Rhodium(I) Catalysis by Planar Chiral Dibenzo[a, e]cyclooctatetraenes


Melcher, Michaela-Christina; Ivšić, Trpimir; Olagnon, Charlotte; Tenten, Christina; Lützen, Arne; Strand, Daniel
Control of Enantioselectivity in Rhodium(I) Catalysis by Planar Chiral Dibenzo[a, e]cyclooctatetraenes // Chemistry : a European journal, 24 (2018), 10; 2344-2348 doi:10.1002/chem.201704816 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 918975 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Control of Enantioselectivity in Rhodium(I) Catalysis by Planar Chiral Dibenzo[a, e]cyclooctatetraenes

Autori
Melcher, Michaela-Christina ; Ivšić, Trpimir ; Olagnon, Charlotte ; Tenten, Christina ; Lützen, Arne ; Strand, Daniel

Izvornik
Chemistry : a European journal (0947-6539) 24 (2018), 10; 2344-2348

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

Ključne riječi
asymmetric catalysis ; cyclooctatetraenes ; fenestrenes ; planar chirality ; rhodium

Sažetak
Planar chiral 5, 11-disubstiuted dibenzo[a, e]cyclo- octatetraenes (dbCOTs) have been developed as the first useful chiral homologs to dbCOT-ligands for asymmetric applications. Methods enabling the preparation of such compounds on a gram-scale in enantiomerically pure form are described. Evaluated as ligands in rhodium(I)-catalyzed 1, 4- and 1, 2-arylation reactions, tertiary and quarternary stereogenic centers were formed with excellent yields and selectivities of up to > 99 % ee. A catalytic asymmetric synthesis of a key cyclization precursor to (À)-penifulvin A highlights the system in an applied context.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Profili:

Avatar Url Trpimir Ivšić (autor)

Poveznice na cjeloviti tekst rada:

doi onlinelibrary.wiley.com doi.org

Citiraj ovu publikaciju:

Melcher, Michaela-Christina; Ivšić, Trpimir; Olagnon, Charlotte; Tenten, Christina; Lützen, Arne; Strand, Daniel
Control of Enantioselectivity in Rhodium(I) Catalysis by Planar Chiral Dibenzo[a, e]cyclooctatetraenes // Chemistry : a European journal, 24 (2018), 10; 2344-2348 doi:10.1002/chem.201704816 (međunarodna recenzija, članak, znanstveni)
Melcher, M., Ivšić, T., Olagnon, C., Tenten, C., Lützen, A. & Strand, D. (2018) Control of Enantioselectivity in Rhodium(I) Catalysis by Planar Chiral Dibenzo[a, e]cyclooctatetraenes. Chemistry : a European journal, 24 (10), 2344-2348 doi:10.1002/chem.201704816.
@article{article, author = {Melcher, Michaela-Christina and Iv\v{s}i\'{c}, Trpimir and Olagnon, Charlotte and Tenten, Christina and L\"{u}tzen, Arne and Strand, Daniel}, year = {2018}, pages = {2344-2348}, DOI = {10.1002/chem.201704816}, keywords = {asymmetric catalysis, cyclooctatetraenes, fenestrenes, planar chirality, rhodium}, journal = {Chemistry : a European journal}, doi = {10.1002/chem.201704816}, volume = {24}, number = {10}, issn = {0947-6539}, title = {Control of Enantioselectivity in Rhodium(I) Catalysis by Planar Chiral Dibenzo[a, e]cyclooctatetraenes}, keyword = {asymmetric catalysis, cyclooctatetraenes, fenestrenes, planar chirality, rhodium} }
@article{article, author = {Melcher, Michaela-Christina and Iv\v{s}i\'{c}, Trpimir and Olagnon, Charlotte and Tenten, Christina and L\"{u}tzen, Arne and Strand, Daniel}, year = {2018}, pages = {2344-2348}, DOI = {10.1002/chem.201704816}, keywords = {asymmetric catalysis, cyclooctatetraenes, fenestrenes, planar chirality, rhodium}, journal = {Chemistry : a European journal}, doi = {10.1002/chem.201704816}, volume = {24}, number = {10}, issn = {0947-6539}, title = {Control of Enantioselectivity in Rhodium(I) Catalysis by Planar Chiral Dibenzo[a, e]cyclooctatetraenes}, keyword = {asymmetric catalysis, cyclooctatetraenes, fenestrenes, planar chirality, rhodium} }

Časopis indeksira:


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


Citati:





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