Organic & Biomolecular Chemistry, our sister journal, publishes many articles that cover natural product chemistry. We will try to keep you updated, although the safest bet is for you to sign up to OBC’s e-alert (free service) and receive the table of content directly in your inbox every time an issue is published.
The latest natural products’ related articles in OBC Issue 11 (coming soon) have been collated here.
If you want to see your natural products article featured on this blog you can submit it here.
Cascade polycyclisations in natural product synthesis
Edward A. Anderson
Org. Biomol. Chem., 2011, Advance Article
DOI: 10.1039/C1OB05212H, Emerging Area
Intramolecular catalytic asymmetric carbon–hydrogen insertion reactions. Synthetic advantages in total synthesis in comparison with alternative approaches
Michael P. Doyle, Maxim Ratnikov and Yu Liu
Org. Biomol. Chem., 2011, Advance Article
DOI: 10.1039/C0OB00698J, Perspective
A family of multicyclic indolosesquiterpenes from a bacterial endophyte
Ling Ding, Armin Maier, Heinz-Herbert Fiebig, Wen-Han Lin and Christian Hertweck
Org. Biomol. Chem., 2011, Advance Article
DOI: 10.1039/C1OB05283G, Communication
Intermolecular radical addition to N-acylhydrazones as a stereocontrol strategy for alkaloid synthesis: formal synthesis of quinine
Gregory K. Friestad, An Ji, Chandra Sekhar Korapala and Jun Qin
Org. Biomol. Chem., 2011, Advance Article
DOI: 10.1039/C1OB05219E, Communication
Free radical 5-exo-dig cyclization as the key step in the synthesis of bis-butyrolactone natural products: experimental and theoretical studies
Gangavaram V. M. Sharma, Devoju Harinada Chary, Nagula Chandramouli, Florian Achrainer, Sateesh Patrudu and Hendrik Zipse
Org. Biomol. Chem., 2011, Advance Article
DOI: 10.1039/C1OB00019E, Paper
Efficient synthesis of esermethole and its analogues
Yongyun Zhou, Yuanhong Zhao, Xiaoyong Dai, Jianping Liu, Liang Li and Hongbin Zhang
Org. Biomol. Chem., 2011, Advance Article
DOI: 10.1039/C1OB05275F, Paper
New insights into ergot alkaloid biosynthesis in Claviceps purpurea: An agroclavine synthase EasG catalyses, via a non-enzymatic adduct with reduced glutathione, the conversion of chanoclavine-I aldehyde to agroclavine
Marco Matuschek, Christiane Wallwey, Xiulan Xie and Shu-Ming Li
Org. Biomol. Chem., 2011, Advance Article
DOI: 10.1039/C0OB01215G, Paper
