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- Publisher Website: 10.1021/acs.orglett.9b00718
- Scopus: eid_2-s2.0-85065015955
- PMID: 30995051
- WOS: WOS:000468696100009
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Article: Azaindenocorannulenes: Synthesis, Properties, and Chirality
Title | Azaindenocorannulenes: Synthesis, Properties, and Chirality |
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Authors | |
Issue Date | 2019 |
Citation | Organic Letters, 2019, v. 21, n. 10, p. 3510-3513 How to Cite? |
Abstract | Palladium-catalyzed intramolecular arylation provides bowl-shaped azaindenocorannulenes 7-9. Crystals of 8 show bowl-in-bowl columnar stacking. A substituent model rationalizes the first reduction potential of 18 related molecular bowls. The absolute configurations of bowls 7 and 9 are correlated with VCD and ECD spectra. The bowl inversion barrier of 9 (>190 kJ/mol) shows it to be more inert configurationally than chiral biaryl, phosphenes, or [n]helicenes. |
Persistent Identifier | http://hdl.handle.net/10722/341491 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.245 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Tian, Xiaoqi | - |
dc.contributor.author | Roch, Loïc M. | - |
dc.contributor.author | Vanthuyne, Nicolas | - |
dc.contributor.author | Xu, Jun | - |
dc.contributor.author | Baldridge, Kim K. | - |
dc.contributor.author | Siegel, Jay S. | - |
dc.date.accessioned | 2024-03-13T08:43:13Z | - |
dc.date.available | 2024-03-13T08:43:13Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Organic Letters, 2019, v. 21, n. 10, p. 3510-3513 | - |
dc.identifier.issn | 1523-7060 | - |
dc.identifier.uri | http://hdl.handle.net/10722/341491 | - |
dc.description.abstract | Palladium-catalyzed intramolecular arylation provides bowl-shaped azaindenocorannulenes 7-9. Crystals of 8 show bowl-in-bowl columnar stacking. A substituent model rationalizes the first reduction potential of 18 related molecular bowls. The absolute configurations of bowls 7 and 9 are correlated with VCD and ECD spectra. The bowl inversion barrier of 9 (>190 kJ/mol) shows it to be more inert configurationally than chiral biaryl, phosphenes, or [n]helicenes. | - |
dc.language | eng | - |
dc.relation.ispartof | Organic Letters | - |
dc.title | Azaindenocorannulenes: Synthesis, Properties, and Chirality | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/acs.orglett.9b00718 | - |
dc.identifier.pmid | 30995051 | - |
dc.identifier.scopus | eid_2-s2.0-85065015955 | - |
dc.identifier.volume | 21 | - |
dc.identifier.issue | 10 | - |
dc.identifier.spage | 3510 | - |
dc.identifier.epage | 3513 | - |
dc.identifier.eissn | 1523-7052 | - |
dc.identifier.isi | WOS:000468696100009 | - |