Canvass: A Crowd-Sourced, Natural-Product Screening Library for Exploring Biological Space

Autor: Sara E. Kearney, Gergely Zahoránszky-Kőhalmi, Kyle R. Brimacombe, Mark J. Henderson, Caitlin Lynch, Tongan Zhao, Kanny K. Wan, Zina Itkin, Christopher Dillon, Min Shen, Dorian M. Cheff, Tobie D. Lee, Danielle Bougie, Ken Cheng, Nathan P. Coussens, Dorjbal Dorjsuren, Richard T. Eastman, Ruili Huang, Michael J. Iannotti, Surendra Karavadhi, Carleen Klumpp-Thomas, Jacob S. Roth, Srilatha Sakamuru, Wei Sun, Steven A. Titus, Adam Yasgar, Ya-Qin Zhang, Jinghua Zhao, Rodrigo B. Andrade, M. Kevin Brown, Noah Z. Burns, Jin K. Cha, Emily E. Mevers, Jon Clardy, Jason A. Clement, Peter A. Crooks, Gregory D. Cuny, Jake Ganor, Jesus Moreno, Lucas A. Morrill, Elias Picazo, Robert B. Susick, Neil K. Garg, Brian C. Goess, Robert B. Grossman, Chambers C. Hughes, Jeffrey N. Johnston, Madeleine M. Joullie, A. Douglas Kinghorn, David G.I. Kingston, Michael J. Krische, Ohyun Kwon, Thomas J. Maimone, Susruta Majumdar, Katherine N. Maloney, Enas Mohamed, Brian T. Murphy, Pavel Nagorny, David E. Olson, Larry E. Overman, Lauren E. Brown, John K. Snyder, John A. Porco, Fatima Rivas, Samir A. Ross, Richmond Sarpong, Indrajeet Sharma, Jared T. Shaw, Zhengren Xu, Ben Shen, Wei Shi, Corey R.J. Stephenson, Alyssa L. Verano, Derek S. Tan, Yi Tang, Richard E. Taylor, Regan J. Thomson, David A. Vosburg, Jimmy Wu, William M. Wuest, Armen Zakarian, Yufeng Zhang, Tianjing Ren, Zhong Zuo, James Inglese, Sam Michael, Anton Simeonov, Wei Zheng, Paul Shinn, Ajit Jadhav, Matthew B. Boxer, Matthew D. Hall, Menghang Xia, Rajarshi Guha, Jason M. Rohde

Publikováno v: ACS Central Science, Vol 4, Iss 12, Pp 1727-1741 (2018)

Externí odkaz: https://doaj.org/article/9f2975f36dd648f0b92b6e0f2b27c087

Natural product synthesis with unnatural results: Characterization of a novel fused imidazolidinone tetrahydropyrroloindole ring system by long-range1H-15N 2D-NMR

Autor: Gary E. Martin, Madeleine M. Joullie, Chad E. Hadden, David J. Richard

Publikováno v: Journal of Heterocyclic Chemistry. 40:359-362

Synthetic efforts towards the indole alkaloid natural product roquefortine C resulted in the formation of an unknown intermediate. Elucidation of the structure of this molecule relied on the use of long-range 1H-15N 2D-NMR. Computational predictions

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7aefb2040ebf6c2a525b3cdefbe8e050
https://doi.org/10.1002/jhet.5570400227

ChemInform Abstract: Analogues of the β-Turn of the Cyclodepsipeptide Didemnin B

Autor: J. M. Ramanjulu, M. M. Joullie

Publikováno v: ChemInform. 27

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5f5aa1d89f64dbd138e0eb91b0978958
https://doi.org/10.1002/chin.199617191

ChemInform Abstract: Syntheses of Acyclic Analogues of Didemnin B

Autor: M. M. Joullie, J. M. Ramanjulu, Wen Ren Li

Publikováno v: ChemInform. 28

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e592ad9cc75755c048a54fa8edd50a74
https://doi.org/10.1002/chin.199748244

ChemInform Abstract: Total Syntheses of Conformationally Constrained Didemnin B. Analogues. Replacements of N,O-Dimethyltyrosine with L-1,2,3,4-Tetrahydroisoquinoline and L-1,2,3,4-Tetrahydro-7-methoxyisoquinoline

Autor: Joullie Madeleine M. Joullie Madeleine M., James E. Tarver, Amy J. Pfizenmayer

Publikováno v: ChemInform. 33

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e9eb5a29babafda7e618a6431eca0493
https://doi.org/10.1002/chin.200216189