Further insight into the asymmetric vinylogous Mukaiyama aldol reaction (VMAR); application to the synthesis of the C27–C45 segment of lagunamide A-Reference-Cited by-同舟云学术

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Further insight into the asymmetric vinylogous Mukaiyama aldol reaction (VMAR); application to the synthesis of the C27–C45 segment of lagunamide A

Published:2016-05 Issue:19 Volume:72 Page:2481-2490
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Banasik Brent A.,Wang Lee,Kanner Arielle,Bergdahl B. Mikael

Funder

San Diego State University Foundation

California State University Program for Education and Research (CSUPERB)

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. Lagunamides A and B: Cytotoxic and Antimalarial Cyclodepsipeptides from the Marine Cyanobacterium Lyngbya majuscula

2. Biochemical Studies of the Lagunamides, Potent Cytotoxic Cyclic Depsipeptides from the Marine Cyanobacterium Lyngbya majuscula

3. Total synthesis and stereochemical revision of lagunamide A

4. Diverse Synthesis of Marine Cyclic Depsipeptide Lagunamide A and Its Analogues

5. An efficient synthesis of the C27–C45 fragment of lagunamide A, a cyclodepsipeptide with potent cytotoxic and antimalarial properties

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1. Structure revision of lagunamide C to odoamide by total synthesis and biological evaluation;Tetrahedron;2024-03

2. Diastereoselective Aldol Reactions;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2022

3. Synthesis and Biological Activities of Cyclodepsipeptides of Aurilide Family from Marine Origin;Marine Drugs;2021-01-23

4. A Straightforward Synthesis of Polyketides via Ester Dienolate Matteson Homologation;Chemistry – A European Journal;2020-12-15

5. 1,2-Anti aldol methodologies used in natural product synthesis;Tetrahedron;2020-01

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