Zobrazeno 1 - 10
of 106
pro vyhledávání: '"Noah Z. Burns"'
Autor:
Yanan Li, Ting Yu, Xi Feng, Bo Zhao, Huahui Chen, Huan Yang, Xing Chen, Xiao-Hua Zhang, Hayden R. Anderson, Noah Z. Burns, Fuxing Zeng, Lizhi Tao, Zhirui Zeng
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-9 (2024)
Abstract Archaea possess characteristic membrane-spanning lipids that are thought to contribute to the adaptation to extreme environments. However, the biosynthesis of these lipids is poorly understood. Here, we identify a radical S-adenosyl-L-methio
Externí odkaz:
https://doaj.org/article/2f89ffe94c9d420681d868d1666fb774
Autor:
Benjamin R. Boswell, Carl M. F. Mansson, Gabrielle E. Cabrera, Calvin R. Hansen, Allen G. Oliver, Noah Z. Burns
Publikováno v:
Journal of the American Chemical Society. 145:5631-5636
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59cd47b93a4e0ade7529f721840ba231
https://doi.org/10.1021/jacs.3c01591
https://doi.org/10.1021/jacs.3c01591
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
Autor:
Sajan C. Patel, Noah Z. Burns
Publikováno v:
Journal of the American Chemical Society. 144:17797-17802
A longstanding challenge in fundamental functional group interconversion has been the direct transformation of benzene into pyridine via nitrogen insertion and carbon deletion. Herein, we report a protocol for the transformation of aryl azides, easil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dae16e6f0c7f10ead9e6325c509b3f9
https://doi.org/10.1021/jacs.2c08464
https://doi.org/10.1021/jacs.2c08464
Autor:
Frederick J. Seidl, Noah Z. Burns
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 1361-1365 (2016)
The scope of a recently reported method for the catalytic enantioselective bromochlorination of allylic alcohols is expanded to include a specific homoallylic alcohol. Critical factors for optimization of this reaction are highlighted. The utility of
Externí odkaz:
https://doaj.org/article/a0838d2da08f42618abdb170591dd492
Autor:
Carl M. F. Mansson, Noah Z. Burns
Publikováno v:
Journal of the American Chemical Society. 144(43)
The Kochi-Salomon reaction is the only photochemical [2+2] cycloaddition capable of combining two electronically unactivated olefins into a cyclobutane. Yet, the reaction has remained largely unexplored and suffers many drawbacks, most notably an int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fb4a0343e1533aa0bae0f12e6c41b7d
https://pubmed.ncbi.nlm.nih.gov/36269089
https://pubmed.ncbi.nlm.nih.gov/36269089
Publikováno v:
Organic Letters. 23:6530-6535
Cyclobutenes are highly useful synthetic intermediates as well as important motifs in bioactive small molecules. Herein, we report a regio-, chemo-, and enantioselective synthesis of cyclobutenes from olefins using N-sulfonyl-1,2,3-triazoles as vicin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44bfd295bfd5cfeb9e5a0c5622e5e084
https://doi.org/10.1021/acs.orglett.1c02331
https://doi.org/10.1021/acs.orglett.1c02331
Autor:
Benjamin R. Boswell, André Eberhard, Noah Z. Burns, Pascal Friederich, Jingbai Li, Patrick Reiser, Steven A. Lopez
Publikováno v:
Chemical Science, 12 (14), 5302-5314
Chemical Science
Chemical Science
Photochemical reactions are widely used by academic and industrial researchers to construct complex molecular architectures via mechanisms that often require harsh reaction conditions. Photodynamics simulations provide time-resolved snapshots of mole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c45a8c13b09d11e72db82267a17fc52a
https://doi.org/10.1039/d0sc05610c
https://doi.org/10.1039/d0sc05610c
Autor:
Gabrielle E. Cabrera, Tristen A. Reid, Eric C. Johnson, Joshua A. Orlicki, Noah Z. Burns, Jesse J. Sabatini
Publikováno v:
ChemPlusChem. 87
The synthesis of 3-(nitratoethyl-N-nitramino)-5-(nitratomethyl) isoxazole (C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::767ebc060d05b22af428f6312cb2640a
https://doi.org/10.1002/cplu.202200096
https://doi.org/10.1002/cplu.202200096
Autor:
Joseph A. H. Romaniuk, Noah Z. Burns, Jordan M. Cox, Carl M. F. Mansson, Yan Xia, Kurt P. Lindquist, Zexin Jin, Lynette Cegelski, Steven A. Lopez, Benjamin R. Boswell
Publikováno v:
Nature Chemistry. 13:41-46
Polymer mechanochemistry has traditionally been employed to study the effects of mechanical force on chemical bonds within a polymer backbone or to generate force-responsive materials. It is under-exploited for the scalable synthesis of wholly new ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::963e0210275afb80dbd3115837f69771
https://doi.org/10.1038/s41557-020-00608-8
https://doi.org/10.1038/s41557-020-00608-8