3,3'-Anisyl-Substituted BINOL, H4BINOL, and H8BINOL Ligands: Asymmetric Synthesis of Diverse Propargylic Alcohols and Their Ring-Closing Metathesis to Chiral Cycloalkenes
- Author
- YANG YUE1 2 ; TURLINGTON, Mark1 ; YU, Xiao-Qi2 ; LIN PU1
[1] Department of Chemistry, University of Virginia, Charlottesville, Virginia 22904, United States
[2] Department of Chemistry, Key Laboratory of Green Chemistry and Technology (Ministry of Education), Sichuan University, Chengdu, China 610064, United States - Source
Journal of organic chemistry. 2009, Vol 74, Num 22, pp 8681-8689, 9 p ; ref : 18 ref
- CODEN
- JOCEAH
- ISSN
- 0022-3263
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Activité optique Alcool Alcyne Aldéhyde Anisole Chimiosélectivité Composé acétylénique Composé chiral Composé propargylique Cyclisation Cycloalcène Enantiosélectivité Etude comparative Excès énantiomère Hydrogénation Ligand Métathèse Phénols Réaction catalytique Réaction tandem Synthèse asymétrique Synthèse chimique Température ambiante 1,1p-Binaphtyle-2,2p-diol Acétylène(phényl) Catalyseur Grubbs Titane IV propan-2-olate Zinc(diéthyl)
- Keyword (en)
- Optical activity Alcohol Alkyne Aldehyde Chemoselectivity Acetylenic compound Chiral compound Propargylic compound Cyclization Cycloalkene Enantioselectivity Comparative study Enantiomeric excess Hydrogenation Ligand Metathesis Phenols Catalytic reaction Tandem reaction Asymmetric synthesis Chemical synthesis Room temperature Grubbs catalyst
- Keyword (es)
- Actividad óptica Alcohol Alquino Aldehído Quimioselectividad Compuesto acetilénico Compuesto quiral Compuesto propargílico Ciclización Cicleno Enantioselectividad Estudio comparativo Exceso enantiómero Hidrogenación Ligando Metatesis Fenoles Reacción catalítica Reacción tándem Síntesis asimétrica Síntesis química Temperatura ambiente
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03B Reactivity and mechanisms / 001C03B02 Kinetics and mechanisms
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C03 Noncondensed benzenic compounds
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C04 Condensed benzenic and aromatic compounds
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05A Alicyclic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 22135704
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1021/jo9018446 
https://dx.doi.org/10.1021/jo9018446
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