Victor Aniebok
University of California, Santa Cruz
4 Papers
2 Citations
Victor Aniebok is an academic researcher from University of California, Santa Cruz. The author has contributed to research in topics: Chemistry & Natural product. The author has an hindex of 2, co-authored 2 publications.
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Papers
The Natural Products Atlas: An Open Access Knowledge Base for Microbial Natural Products Discovery.
Jeffrey A. van Santen,Gregoire Jacob,Amrit Leen Singh,Victor Aniebok,Marcy J. Balunas,Derek Bunsko,Fausto Carnevale Neto,Fausto Carnevale Neto,Fausto Carnevale Neto,Laia Castano-Espriu,Chen Chang,Trevor N. Clark,Jessica C. Little,David A. Delgadillo,Pieter C. Dorrestein,Katherine R. Duncan,Joseph M. Egan,Melissa M. Galey,F. P. Jake Haeckl,Alex Hua,Alison H. Hughes,Dasha Iskakova,Aswad S Khadilkar,Jung-Ho Lee,Sanghoon Lee,Nicole LeGrow,Dennis Y. Liu,Jocelyn Macho,Catherine McCaughey,Marnix H. Medema,Ram P. Neupane,Timothy J. O’Donnell,Jasmine S. Paula,Laura M. Sanchez,Anam F. Shaikh,Sylvia Soldatou,Barbara R. Terlouw,Tuan Anh Tran,Tuan Anh Tran,Mercia C. Valentine,Justin J. J. van der Hooft,Duy A. Vo,Mingxun Wang,Darryl Wilson,Katherine E. Zink,Roger G. Linington +45 more
TL;DR: The Natural Products Atlas is designed as a community-supported resource to provide a central repository for known natural product structures from microorganisms and is the first comprehensive, open access resource of this type.
Nonenzymatic Reactions in Natural Product Formation.
TL;DR: This review will cover recent nonenzymatic biosynthetic mechanisms and include sources for those reviewed previously.
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Synthesis and Investigation of the Abiotic Formation of Pyonitrins A-D
TL;DR: This work has accomplished the first biomimetic total synthesis of pyonitrins A–D in three steps and studied the nonenzymatic formation of the pyon itrins using 15N NMR spectroscopy.
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Biomimetic Total Synthesis and Investigation of the Non‐Enzymatic Chemistry of Oxazinin A
TL;DR: The first total synthesis of an antimycobacterial natural product oxazinin A is reported, that takes advantage of a multi‐component cascade reaction of anthranilic acid and a precursor polyketide containing an aldehyde.
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