Results 61 to 70 of about 1,974 (174)
Preparation and Synthetic Applications of 8-Oxabicyclo[3.2.1]oct-6-en-3-one Derivatives
The development of efficient routes to multi-gram quantities of chiral synthons is a key issue in the total synthesis of natural products and analogues.
Sylvain Favre +2 more
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Synthesis of chiral sulfoximine-based thioureas and their application in asymmetric organocatalysis
For the first time, chiral sulfoximine derivatives have been applied as asymmetric organocatalysts. In combination with a thiourea-type backbone the sulfonimidoyl moiety leads to organocatalysts showing good reactivity in the catalytic desymmetrization ...
Marcus Frings +2 more
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meso-exo-3,5-dihydroxymethylenetricyclo[5.2.1.0(2,6)]decane was efficiently desymmetrized by the lipase from Pseudomonas cepacia (PS-C 'Amano' II) in vinyl acetate in high yields (93%) and with excellent enantiomeric excesses (ee > 99% by chiral GC ...
Costa Valentim E. U +2 more
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An approach utilizing N-heterocyclic carbene for nitrile formation and desymmetrization reaction is developed. The process involves kinetic resolution, with the axially chiral aryl monoaldehydes obtained in moderate yields with excellent optical purities.
Yuanlin Cai +5 more
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A palladium/TADDOL-derived phosphonate catalyzed desymmetric ring-opening coupling bewteen prochiral silacyclobutanes and alkyl terminal alkynes was developed.
Zhi-Yuan Chen +3 more
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Procrystalline Self-Assembly of Desymmetrized Pentaphenylcyclopentadiene
The interplay between the molecular shape and the intermolecular interaction plays a decisive role in self-assembled structures. Recently, inherent randomness of low ordered assemblies, resulting from lack of short- and long-range periodicities, has attracted significant attention due to the unique structural, electronic, and mechanical properties ...
Li, Donglin +6 more
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Catalytic asymmetric desymmetrization of diesters: advances and perspectives
Catalytic asymmetric desymmetrization of prochiral and meso-diesters has emerged as a powerful strategy for the synthesis of chiral compounds featuring tertiary or quaternary stereogenic carbon centers.
Yu Huang, Jia-Yu Liao
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Enantioselective synthesis of chiral
The C–N axial chirality is widely present in natural products, bioactive molecules, and chiral ligands. Catalytic asymmetric construction of C–N axially chiral compounds is a challenging task due to the lower rotational barriers of the C–N bond. Here, we
Zi-Wei He +4 more
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Total Synthesis of 4-epi-Bengamide E
Bengamide E is a bioactive natural product that was isolated from Jaspidae sponges by Crews and co-workers in 1989. It displays a wide range of biological activities, including antitumor, antibiotic, and anthelmintic properties.
Gabriella Vitali Forconesi +8 more
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Recent Advances in Enantioselective Desymmetrization Enabled by Chiral Phosphoric Acid Catalysis. [PDF]
Zhang D, Xu B, Yang Y, Zhang D.
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