Comment on Enantioselective total synthesis of (−)-colchicine, (+)-demecolcinone and metacolchicine: determination of the absolute configurations of the latter two alkaloids by B. Chen, X. Liu, Y.-J. Hu, D.-M. Zhang, L. Deng, J. Lu, L. Min, W.-C. Ye and C.-C. Li, Chem. Sci., 2017, 8, 4961–4966
Author:
Affiliation:
1. Fachbereich Chemie der Philipps Universität Marburg
2. D-35032 Marburg
3. Germany
4. Department of Chemistry
5. University of Cologne
6. D-50939 Koeln
7. The Centre for Advanced Imaging
8. The University of Queensland
9. St. Lucia
10. Australia
Abstract
We note that some features of the NMR spectra deposited for the purported isomeric metacolchicines are not compatible with the assignment of those isomers as being atrop-diastereomers.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/SC/C8SC90247J
Reference7 articles.
1. Metacolchicine, a New Colchicinoid from Sandersonia aurantiaca
2. Enantioselective total synthesis of (−)-colchicine, (+)-demecolcinone and metacolchicine: determination of the absolute configurations of the latter two alkaloids
3. Isolation of atropisomers in both the isocolchicide and colchicide series of alkaloids and determination of their chiroptical properties
4. Stereochemical variations on the colchicine motif. Peracid oxidation of thiocolchicone. Synthesis, conformation and inhibition of microtubule assembly
5. Conformational isomerism and its relation to the mutarotation of isocolchicine
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4. Correction: Enantioselective total synthesis of (−)-colchicine, (+)-demecolcinone and metacolchicine: determination of the absolute configurations of the latter two alkaloids;Chemical Science;2019
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