The mechanism and origin of selectivities for NHC-catalyzed synthesis of axially chiral benzothiophene/benzofuran-fused biaryls. Issue 8 (8th February 2022)
- Record Type:
- Journal Article
- Title:
- The mechanism and origin of selectivities for NHC-catalyzed synthesis of axially chiral benzothiophene/benzofuran-fused biaryls. Issue 8 (8th February 2022)
- Main Title:
- The mechanism and origin of selectivities for NHC-catalyzed synthesis of axially chiral benzothiophene/benzofuran-fused biaryls
- Authors:
- Zhang, Jiaming
Qiao, Qinyu
Wu, Zhoujie
Pang, Zhou
Shi, Qianqian
Wang, Yanyan
Qiao, Yan
Wei, Donghui - Abstract:
- Abstract : DFT calculations were performed to investigate the actual mechanism of organocatalytic intermolecular [2 + 4] cyclization for the synthesis of axially chiral benzothiophene-fused biaryls using enal and 2-benzyl-benzothiophene-3-carbaldehyde. Abstract : By performing density functional theory (DFT) calculations, we investigated and identified the fundamental pathway for N-heterocyclic carbene (NHC)-catalyzed synthesis of axially chiral benzothiophene-fused biaryls using enal and 2-benzyl-benzothiophene-3-carbaldehyde, which includes (1) nucleophilic attack on enal by the organocatalyst NHC, (2) [1, 2]-proton transfer, (3) oxidation, (4) stereoselective formation of the C–C σ bond, (5) intramolecular [2 + 2] cycloaddition, (6) dissociation of NHC, (7) release of CO2, and (8) transformation to axial chirality. Moreover, the calculated results can reasonably explain the observed chemo- and stereoselectivities for the formation of both benzothiophene/benzofuran-fused biaryls in these kinds of reactions. Further non-covalent interaction (NCI) and atoms-in-molecules (AIM) analyses demonstrate that the hydrogen bond interactions are responsible for the stability of key stereoselective transition states. This work would be useful for understanding the origin of stereoselectivity of NHC-catalyzed intermolecular cyclization reactions for the synthesis of axially benzothiophene/benzofuran-fused biaryl compounds.
- Is Part Of:
- Organic & biomolecular chemistry. Volume 20:Issue 8(2022)
- Journal:
- Organic & biomolecular chemistry
- Issue:
- Volume 20:Issue 8(2022)
- Issue Display:
- Volume 20, Issue 8 (2022)
- Year:
- 2022
- Volume:
- 20
- Issue:
- 8
- Issue Sort Value:
- 2022-0020-0008-0000
- Page Start:
- 1662
- Page End:
- 1670
- Publication Date:
- 2022-02-08
- Subjects:
- Chemistry, Organic -- Periodicals
Bioorganic chemistry -- Periodicals
Chemistry, Physical organic -- Periodicals
547 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ob#!recentarticles&all ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1ob02429a ↗
- Languages:
- English
- ISSNs:
- 1477-0520
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6286.350000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21048.xml