Enantioselective Synthesis of a New Non-Natural Gabosine
The preparation of a new non-natural gabosine is reported, in which the chirality is transferred from the toluene’s biotransformed metabolite (1<i>R</i>,2<i>S</i>)-<i>3</i>-methylcyclohexa-3.5-diene-1,2-diol. Further chemical transformations to introduce additiona...
Main Authors: | Maximiliano Colobbio, Enrique Pandolfi, Valeria Schapiro |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-03-01
|
Series: | Molecules |
Subjects: | |
Online Access: | https://www.mdpi.com/1420-3049/26/5/1423 |
Similar Items
-
Total Synthesis of Bio-active Natural Products Gabosines, Crassalactone C, Anamarine and Iriomoteolide 3a
by: Kumar, S Mothish
Published: (2018) -
Applications of Bolm’s Ligand in Enantioselective Synthesis
by: Eva Bednářová, et al.
Published: (2020-02-01) -
New Concepts, Catalysts, and Methods for Enantioselective Synthesis of C-B and C-C Bonds
by: Radomkit, Suttipol
Published: (2016) -
Development and Application of Methods for Enantioselective Synthesis of Amines and Alcohols:
by: Morrison, Ryan John
Published: (2020) -
Enantioselective Synthesis of the C(1)-C(6?) Subunit of Zaragozic Acid C
by: Carreira Erick M., et al.
Published: (1998-01-01)