Atropselective syntheses of (−) and (+) rugulotrosin A utilizing point-to-axial chirality transfer-Reference-Cited by-同舟云学术

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Atropselective syntheses of (−) and (+) rugulotrosin A utilizing point-to-axial chirality transfer

Published:2015-02-02 Issue:3 Volume:7 Page:234-240
ISSN:1755-4330
Container-title:Nature Chemistry
language:en
Short-container-title:Nature Chem

Author:

Qin Tian,Skraba-Joiner Sarah L.,Khalil Zeinab G.,Johnson Richard P.,Capon Robert J.,Porco John A.

Publisher

Springer Science and Business Media LLC

Subject

General Chemical Engineering,General Chemistry

Link

http://www.nature.com/articles/nchem.2173.pdf

Reference48 articles.

1. Moss, G. P. Basic terminology of stereochemistry. Pure Appl. Chem. 68, 2193–2222 (1996).

2. Zask, A., Murphy, J. & Ellestad, G. A. Biological stereoselectivity of atropisomeric natural products and drugs. Chirality 25, 265–274 (2013).

3. Clayden, J., Moran, W. J., Edwards, P. J. & LaPlante, S. R. The challenge of atropisomerism in drug discovery. Angew. Chem. Int. Ed. 48, 6398–6401 (2009).

4. LaPlante, S. R., Edwards, P. J., Fader, L. D., Jakalian, A. & Hucke, O. Revealing atropisomer axial chirality in drug discovery. ChemMedChem 6, 505–513 (2011).

5. Bringmann, G. et al. Atroposelective synthesis of axially chiral biaryl compounds. Angew. Chem. Int. Ed. 44, 5387–5427 (2005).

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