Stereoselective Synthesis and Antiproliferative Activity of Steviol-Based Diterpene 1,3-Aminoalcohol Regioisomers
A series of novel diterpene-type 1,3-aminoalcohols and their regioisomers have been synthesised from natural stevioside in a stereoselective manner. The key intermediate β-keto alcohol was prepared using Wagner–Meerwein rearrangement of the epoxide derived from steviol methyl ester. The primary amin...
Main Authors: | Dorottya Bai, Zsuzsanna Schelz, Mária Fanni Boncz, István Zupkó, Zsolt Szakonyi |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2023-12-01
|
Series: | Molecules |
Subjects: | |
Online Access: | https://www.mdpi.com/1420-3049/28/24/7962 |
Similar Items
-
Synthesis and Study of the Structure–Activity Relationship of Antiproliferative <i>N</i>-Substituted Isosteviol-Based 1,3-Aminoalcohols
by: Dániel Ozsvár, et al.
Published: (2024-02-01) -
Stereoselective Synthesis and Cytoselective Toxicity of Monoterpene-Fused 2-Imino-1,3-thiazines
by: Zsolt Szakonyi, et al.
Published: (2014-10-01) -
Aspirination of α-Aminoalcohol (Sarpogrelate M1)
by: Sunhwa Park, et al.
Published: (2016-08-01) -
Steviol, the aglycon of steviol glycosides, does not reduce hyperglycemia in mice with type 2 diabetes
by: Caroline Simoens, et al.
Published: (2022-11-01) -
Nuevos aminoalcoholes y amidas de la serie y-piperidinica
by: Vladimir Kouznelsov, et al.
Published: (2010-09-01)