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Craig J. Forsyth

Affiliations: 
Chemistry & Biochemistry Ohio State University, Columbus, Columbus, OH 
Area:
Synthetic Organic Chemistry and Chemical Biology
Website:
http://chemistry.osu.edu/faculty/forsyth
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"Craig Forsyth"
Bio:

http://cancer.osu.edu/research/cancerresearch/researchprograms/experimentaltherapeutics/members/Pages/index.aspx?mid=2599

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Parents

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Jon C. Clardy grad student 1989 Cornell
 (Enantioselective total syntheses of didemnenones A and B : absolute configurations of the didemnenones)
Yoshito Kishi post-doc 1992 Harvard

Children

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Yongfeng Li grad student 2001-2006 UMN
Jianyan Xu grad student 2001-2006 UMN
Bo Wang grad student 2002-2006 UMN
Ce Wang grad student 2002-2006 UMN
Lu Ying grad student 2002-2006 UMN
Daniel J. Wherritt grad student 2007-2010 Ohio State
Feng Zhou grad student 2007-2010 Ohio State
Yue Ding grad student 2007-2011 Ohio State
Chao Fang grad student 2007-2011 Ohio State
Yucheng Pang grad student 2007-2011 Ohio State
Ting Wang grad student 2007-2011 Ohio State
Brandon G. Van Ness grad student 2012 Ohio State
Dimao Wu grad student 2012 Ohio State
Zhigao Zhang grad student 2013 Ohio State
Daniel Adu Ampratwum grad student 2010-2016 Ohio State
Li Xiao grad student 2012-2017 Ohio State
Kedwin Rosa Pagan grad student 2012-2018 Ohio State
Nathaniel Thomas Kenton grad student 2013-2018 Ohio State
Bo Wang post-doc 2007-2011 Ohio State

Collaborators

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Publications

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Itskanov S, Wang L, Junne T, et al. (2023) A common mechanism of Sec61 translocon inhibition by small molecules. Nature Chemical Biology
Okumu AA, Forsyth CJ. (2019) Synthesis of the C1-C19 Domain of Azaspiracid-34. Organic Letters
Kenton NT, Adu‐Ampratwum D, Okumu AA, et al. (2018) Total Synthesis of (6 R ,10 R ,13 R ,14 R ,16 R ,17 R ,19 S ,20 R ,21 R ,24 S , 25 S ,28 S ,30 S ,32 R ,33 R ,34 R ,36 S ,37 S ,39 R )‐Azaspiracid‐3 Reveals Non‐Identity with the Natural Product Angewandte Chemie. 130: 805-809
Kenton NT, Adu-Ampratwum D, Okumu AA, et al. (2017) Total Synthesis of (6R,10R,13R,14R,16R,17R,19S,20R,21R,24S, 25S,28S,30S,32R,33R,34R,36S,37S,39R)-Azaspiracid-3 Reveals Non-Identity with the Natural Product. Angewandte Chemie (International Ed. in English)
Kenton NT, Adu-Ampratwum D, Okumu AA, et al. (2017) Stereochemical Definition of the Natural Product (6R,10R,13R, 14R,16R,17R,19S,20S,21R,24S,25S,28S,30S,32R,33R,34R,36S,37S,39R)-Azaspiracid-3 by Total Synthesis and Comparative Analyses. Angewandte Chemie (International Ed. in English)
Akwaboah DC, Wu D, Forsyth CJ. (2017) Stereoselective Synthesis of the C1-C9 and C11-C25 Fragments of Amphidinolides C, C2, C3, and F. Organic Letters
Twiner MJ, Doucette GJ, Pang Y, et al. (2016) Structure-Activity Relationship Studies Using Natural and Synthetic Okadaic Acid/Dinophysistoxin Toxins. Marine Drugs. 14
Line N, Burns A, Butler S, et al. (2016) Total Synthesis of (-)-Salvinorin A. Chemistry (Weinheim An Der Bergstrasse, Germany)
Zhang Z, Chen Y, Adu-Ampratwum D, et al. (2016) Synthesis of the C22-C40 Domain of the Azaspiracids. Organic Letters
Samdal IA, Løvberg KE, Briggs LR, et al. (2015) Development of an ELISA for the Detection of Azaspiracids. Journal of Agricultural and Food Chemistry. 63: 7855-61
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