An improved synthesis and resolution of (±)-cis,cis-2,2′-spirobiindane-1,1′-diol
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference28 articles.
1. An improved synthesis and resolution of (±)-cis,cis-spiro[4.4]nonane-1,6-diol
2. Determination of absolute configuration and enantiomeric purity of spirocyclic alcohols by 1h nmr
3. Absolute stereochemistry of 2,2′-spirobi-indane-1,1′-diols as determined by the C.D. exciton chirality method
4. 2-CARBETHOXYCYCLOOCTANONE
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1. Construction of Annulated Spiro[4.4]-nonane-diones via the Tandem [4 + 2]-Cycloaddition/Aromatization Reaction;The Journal of Organic Chemistry;2023-07-18
2. Catalytic Enantioselective Steglich-Type Rearrangement of Enol Lactones: Asymmetric Synthesis of Spirocyclic 1,3-Diketones;The Journal of Organic Chemistry;2022-11-03
3. Gold(I)-Catalyzed Tandem Intramolecular Methoxylation/Double Aldol Condensation Strategy Yielding 2,2′-Spirobi[indene] Derivatives;Organic Letters;2022-09-14
4. P2O5-Promoted Cyclization of Di[aryl(hetaryl)methyl] Malonic Acids as a Pathway to Fused Spiro[4.4]nonane-1,6-Diones;The Journal of Organic Chemistry;2022-02-15
5. Highly Enantioselective Oxidation of Spirocyclic Hydrocarbons by Bioinspired Manganese Catalysts and Hydrogen Peroxide;ACS Catalysis;2018-02-16
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