Catalytic Enantioselective Synthesis of (−)-Prostaglandin E1 Methyl Ester Based on a Tandem 1,4-Addition−Aldol Reaction [PDF]
Leggy A. Arnold+3 more
openalex +1 more source
Facile enantioselective synthesis of multi-substituted norbornanes/norbornenes using a latent synthon strategy. [PDF]
Shen ZA, Guo J, Lu Y.
europepmc +1 more source
Asymmetric Synthesis of Propargylic and Allenic Silanes, Germanes, and Stannanes
Organotetrel compounds are important reagents with broad applications in chemical industries and natural product synthesis. This review provides a summary of strategies for the synthesis of propargylic and allenic organotetrels in their enantioenriched forms.
Hai Chang, Ruihan Wang, Yi‐Ming Wang
wiley +1 more source
Enantioselective Synthesis of vic-Aminoalcohol Derivatives by Nickel-Catalyzed Reductive Coupling of Aldehydes with Protected Amino-pentadienoates. [PDF]
Bender T, Fürstner A.
europepmc +1 more source
Reusable Selenenyl Iodide‐Initiated Cascade Cyclization of Polyenes with N‐terminating Groups
A cascade cyclization of polyenes with N‑terminating groups, initiated by an isolable selenenyl iodide, was developed. The cavity‑shaped substituent stabilized both the selenenyl iodide and the selenenic acid generated via β‑selenoxide elimination, enabling the regeneration of selenenyl iodide.
Satoru Kuwano+4 more
wiley +1 more source
Organocatalytic skeletal reorganization for enantioselective synthesis of S-stereogenic sulfinamides. [PDF]
Liu Z+6 more
europepmc +1 more source
We report two chiral NCS compounds, (R)‐Sb and (S)‐Sb, featuring aligned Sb3⁺ lone pairs and hydrogen‐bonded [SbOF₃] polyhedra with 4‐hydroxyphenylglycine. These structures exhibit strong SHG (2.6 × KDP), a wide band gap (4.19 eV), and suitable birefringence (0.184@546.1 nm), highlighting the potential of Sb3⁺‐based hybrids for NLO applications ...
Seoyeon Choi, Kang Min Ok
wiley +1 more source
Highly Enantioselective Synthesis of 3,3-Diarylpropyl Amines and 4-Aryl Tetrahydroquinolines via Ir-Catalyzed Asymmetric Hydrogenation. [PDF]
Sidro M+5 more
europepmc +1 more source