Unveiling the Reaction Mechanism of the Das/Chechik/Marek Synthesis of Stereodefined Quaternary Carbon Centers
The reaction mechanism of the Cu<sup>+</sup>-catalyzed introduction of two all-carbon-substituted stereocenters in an ynamide system using a Grignard reagent, a zinc carbenoid, and an aldehyde, was investigated using density-functional theory. In contrast to the formation of an organocop...
Main Authors: | Pedro J. Silva, Carlos E. P. Bernardo |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-05-01
|
Series: | Applied Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/2076-3417/11/11/5002 |
Similar Items
-
Methylene Insertion into Nitrogen‐Heteroatom Single Bonds of 1,2‐Azoles via a Zinc Carbenoid: An Alternative Tool for Skeletal Editing
by: Masato Tsuda, et al.
Published: (2024-03-01) -
Radical zinc-atom-transfer-based carbozincation of haloalkynes with dialkylzincs
by: Fabrice Chemla, et al.
Published: (2013-02-01) -
Diastereo- and enantioselective preparation of cyclopropanol derivatives
by: Marwan Simaan, et al.
Published: (2019-03-01) -
Inserção C-H de carbenóides de ródio em água e reutilização do catalisador Rhodium (II) carbene C-H insertion in water and catalyst reuse
by: Nuno R. Candeias, et al.
Published: (2007-01-01) -
Synthesis of Novel C/D Ring Modified Bile Acids
by: Roselis A. Landaeta Aponte, et al.
Published: (2022-04-01)