Nuclear magnetic resonance assignment strategy for pentacyclic triterpenes, using lup-20(29)-ene from Pilotrichella flexilis as model system, combining spectrally filtered proton-to-carbon schemes and DFT

Nuclear magnetic resonance assignment strategy for pentacyclic triterpenes, using lup-20(29)-ene from Pilotrichella flexilis as model system, combining spectrally filtered proton-to-carbon schemes and DFT–GIAO approach

Published:2019-05-11 Issue:1 Volume:62 Page:
ISSN:2468-0834
Container-title:Applied Biological Chemistry
language:en
Short-container-title:Appl Biol Chem

Author:

Herbert-Pucheta Jose Enrique^ORCID,Mejía-Lara Cinthia,Reyes-Trejo Benito,Reyes Lino,Zuleta-Prada Holber

Funder

CONACYT

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Biochemistry, Genetics and Molecular Biology

Link

http://link.springer.com/content/pdf/10.1186/s13765-019-0435-3.pdf

Reference39 articles.

1. Hill RA, Connolly JD (2018) Triterpenoids. Nat Prod Rep. https://doi.org/10.1039/C8NP00029H

2. Hill RA, Connolly JD (2017) Triterpenoids. Nat Prod Rep 34:90–122

3. Hill RA, Connolly JD (2015) Triterpenoids. Nat Prod Rep 32:273–327

4. Hill RA, Connolly JD (2013) Triterpenoids. Nat Prod Rep 30:1028–1065

5. Hill RA, Connolly JD (2012) Triterpenoids. Nat Prod Rep 29:780–818

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