Configurational analysis of the natural product passifloricin A by quantum mechanical 13C NMR GIAO chemical shift calculations
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Passifloricins, polyketides α-pyrones from Passiflora foetida resin
2. On the Structure of Passifloricin A: Asymmetric Synthesis of the δ-Lactones of (2Z,5S,7R,9S,11S)- and (2Z,5R,7R,9S,11S)-Tetrahydroxyhexacos-2-enoic Acid
3. Enantioselective allyltitanations: synthesis of the proposed structures for passifloricin A
4. Stereochemical analysis of natural products. Approaches relying on the combination of NMR spectroscopy and computational methods
5. Determination of the Relative Stereochemistry of Flexible Organic Compounds by Ab Initio Methods: Conformational Analysis and Boltzmann-Averaged GIAO 13C NMR Chemical Shifts GIAO=gauge including atomic orbitals.
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