scholarly journals Synthesis-Guided Structure Revision of the Sarcodonin, Sarcoviolin, and Hydnellin Natural Product Family

2011 ◽  
Vol 76 (4) ◽  
pp. 1013-1030 ◽  
Author(s):  
David W. Lin ◽  
Takeshi Masuda ◽  
Moritz B. Biskup ◽  
Jonathan D. Nelson ◽  
Phil S. Baran
ChemInform ◽  
2003 ◽  
Vol 34 (3) ◽  
Author(s):  
Hiromasa Kiyota ◽  
Darren J. Dixon ◽  
Christine K. Luscombe ◽  
Stephan Hettstedt ◽  
Steven V. Ley

2013 ◽  
Vol 15 (21) ◽  
pp. 5610-5612 ◽  
Author(s):  
Ruomeng Wang ◽  
Michael N. Paddon-Row ◽  
Michael S. Sherburn

2002 ◽  
Vol 4 (19) ◽  
pp. 3223-3226 ◽  
Author(s):  
Hiromasa Kiyota ◽  
Darren J. Dixon ◽  
Christine K. Luscombe ◽  
Stephan Hettstedt ◽  
Steven V. Ley

2017 ◽  
Vol 149 (4) ◽  
pp. 737-748 ◽  
Author(s):  
Zuzana Barbuščáková ◽  
Hana Kozubíková ◽  
František Zálešák ◽  
Karel Doležal ◽  
Jiří Pospíšil

Synlett ◽  
2017 ◽  
Vol 28 (06) ◽  
pp. 654-663 ◽  
Author(s):  
Rainer Schobert ◽  
Markus Petermichl

2011 ◽  
Vol 76 (13) ◽  
pp. 5283-5294 ◽  
Author(s):  
Philip Garner ◽  
H. Ümit Kaniskan ◽  
Charles M. Keyari ◽  
Laksiri Weerasinghe

2016 ◽  
Vol 52 (85) ◽  
pp. 12638-12641 ◽  
Author(s):  
Xiao-Bo Ding ◽  
Daniel P. Furkert ◽  
Margaret A. Brimble

The heronapyrroles are a family of antibiotic natural products containing the rare 2-nitropyrrole motif.


1994 ◽  
Vol 47 (5) ◽  
pp. 933 ◽  
Author(s):  
R Davis ◽  
RJ Capon

A reinvestigation of the known marine natural product strobilinin has revealed it not to be a single compound (2), but to consist of two naturally occurring geometric isomers, neither of which corresponds to the structure originally assigned. These isomers, (8E,13Z,20Z)- strobilinin (10) and (8Z,13E,20Z)-strobilinin (11), were resolved, characterized and identified as their respective acetate derivatives (6) and (7), and their structures assigned by spectroscopic analysis. It would appear that the absolute stereochemistry of the strobilinins is very likely opposite to that of co-occurring variabilin (1).


ChemInform ◽  
2006 ◽  
Vol 37 (6) ◽  
Author(s):  
Ole A. Andersen ◽  
Mark J. Dixon ◽  
Ian M. Eggleston ◽  
Daan M. F. van Aalten

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