First Stereoselective Total Synthesis of Marliolide-(4R,5R,3E)‑4-hydroxy-5-methyl-3-tetradecylidenedihydrofuran-2(3H)‑one and Vittarilide-B: A Unified Strategy Utilizing a Chiral Pool Approach
Saved in:
Main Authors: | Janardana Reddi Desireddi, Mora Mallikarjuna Rao, Kiran Kumar Murahari, Shivanagababu Challa, Bhimcharan Maiti, Ravinder Manchal |
---|---|
Format: | Article |
Language: | English |
Published: |
American Chemical Society
2025-01-01
|
Series: | ACS Omega |
Online Access: | https://doi.org/10.1021/acsomega.4c10876 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Interspecies In Vitro Evaluation of Stereoselective Protein Binding for 3,4-Methylenedioxymethamphetamine
by: Wan Raihana Wan Aasim, et al.
Published: (2017-01-01) -
5, 4, 3...
by: Alejandra Santana, et al.
Published: (2005-01-01) -
Crystal structure and Hirshfeld surface analysis of 1,3,3,4,4,5,5-heptafluoro-2-(3-[(2,3,3,4,4,5,5-heptafluorocyclopenten-1-yl)oxy]-2-{[(2,3,3,4,4,5,5-heptafluorocyclopenten-1-yl)oxy]methyl}-2-methylpropoxy)cyclopentene
by: Andrew J. Peloquin, et al.
Published: (2025-01-01) -
On the Stability of L4,5 in the Relativistic R3BP with Oblate Secondary and Radiating Primary
by: Nakone Bello, et al.
Published: (2015-01-01) -
[15,8,(4×5,3×4,1×3)]和[15,8,(3×5,5×4)]LUEP码不是最好的
by: 杨劲松, et al.
Published: (1993-01-01)