An Update: Enzymatic Synthesis for Industrial Applications
Supported by rapid technological advancements, biocatalytic applications have matured into a sustainable, scalable, and cost‐competitive alternatives to established chemical catalysis. This review presents the most recent examples of enzyme‐based solutions for the manufacturing of molecules with extended carbon‐carbon frameworks and multiple ...
Thomas Bayer+4 more
wiley +1 more source
Catalytic Enantioselective Synthesis of 1,4-(Hetero) Dicarbonyl Compounds through α-Carbonyl Umpolung. [PDF]
Friedmann T+4 more
europepmc +1 more source
An enantioselective synthesis of isoquinuclidines from 3-substituted chiral pyridinium salts [PDF]
Daniela Cristina dos Santos+3 more
openalex +1 more source
De Novo Enantioselective Synthesis of Hexafluorinated d-Glucose. [PDF]
Depienne S+4 more
europepmc +1 more source
One-pot Enantioselective Synthesis of Optically Active Homoallylic Alcohols from Allyl Halides.
Makoto KANAJIMA+2 more
openalex +2 more sources
Some newer aspects of organozirconium chemistry of relevance to organic synthesis. Zr-Catalyzed enantioselective carbometallation [PDF]
Ei‐ichi Negishi
openalex +1 more source
Highly Enantioselective Organocatalysis with Bidentate Halogen Bond Donors
As the employment of ”non‐classical” non‐covalent interactions like halogen bonding (XB) in asymmetric catalysis is still at a very early stage, there are significant challenges to overcome. In some reported cases, the relevance of halogen bonding to the catalytic action is unclear, while in others, catalyst activity is limited.
Julian Wolf+6 more
wiley +1 more source
Microwave-Assisted Enantioselective Synthesis of (2<i>R</i>,5<i>S</i>)-Theaspirane: A Green Chemistry Approach. [PDF]
Takada SCS+5 more
europepmc +1 more source
1,2-Diborylsilanes: Catalytic Enantioselective Synthesis and Site-Selective Cross-Coupling. [PDF]
Kong Z, Hu W, Morken JP.
europepmc +1 more source
The total synthesis of isodaphlongamine H based on a lactam strategy, which enables quick access to complex cyclic amines, is described. The strategy begins with alkylation of a chiral lactam and subsequent N‐oxidation via an imino ether to afford the N‐hydroxylactam.
Sora Iwamoto+15 more
wiley +1 more source