Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Elias Picazo"'
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-8 (2024)
Abstract Donor-acceptor Stenhouse adducts (DASAs) are molecular photoswitches spurring wide interest because of their dynamic photophysical properties, complex photoswitching mechanism, and diverse applications. Despite breakthroughs in modularity fo
Externí odkaz:
https://doaj.org/article/8870e26b6ef247c195a3ee2e5a659ac7
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:
Elias Picazo
Publikováno v:
Journal of Biological Chemistry. 299:103252
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cf4c4ded758aa14e43ec350600c11d3
https://doi.org/10.1016/j.jbc.2023.103252
https://doi.org/10.1016/j.jbc.2023.103252
Autor:
Rajarshi Guha, Anton Simeonov, Jesus Moreno, Min Shen, Yi Tang, James Inglese, Jared T. Shaw, Jimmy Ming-Tai Wu, Samir A. Ross, Tobie D. Lee, Surendra Karavadhi, Dorian M. Cheff, Susruta Majumdar, Adam Yasgar, Richard E. Taylor, Sam Michael, Zhengren Xu, Wei Sun, Lucas A. Morrill, David A. Vosburg, Wei Zheng, Corey R. J. Stephenson, Noah Z. Burns, Michael J. Iannotti, Carleen Klumpp-Thomas, Richard T. Eastman, Ohyun Kwon, Armen Zakarian, Yufeng Zhang, Matthew D. Hall, Sara E. Kearney, Ya Qin Zhang, Tongan Zhao, Ken Cheng, Indrajeet Sharma, Nathan P. Coussens, Ruili Huang, Derek S. Tan, Paul Shinn, Michael J. Krische, Caitlin Lynch, Jon Clardy, Larry E. Overman, Kanny K. Wan, Chambers C. Hughes, Madeleine M. Joullié, Thomas J. Maimone, Matthew B. Boxer, Jason A. Clement, A. Douglas Kinghorn, Peter A. Crooks, Brian C. Goess, Robert B. Susick, Gergely Zahoránszky-Kőhalmi, Alyssa L. Verano, Danielle Bougie, Jacob S. Roth, Ben Shen, Dorjbal Dorjsuren, Elias Picazo, Jinghua Zhao, John K. Snyder, Rodrigo B. Andrade, Wei Shi, Jin K. Cha, Brian T. Murphy, Fatima Rivas, William M. Wuest, Jake Ganor, Robert B. Grossman, Pavel Nagorny, Emily Mevers, Enas I. Mohamed, David E. Olson, John A. Porco, Neil K. Garg, Srilatha Sakamuru, Jason M. Rohde, M. Kevin Brown, Menghang Xia, Tianjing Ren, Steve Titus, Christopher Dillon, Mark J. Henderson, Zhong Zuo, Regan J. Thomson, David G. I. Kingston, Lauren E. Brown, Jeffrey N. Johnston, Katherine N. Maloney, Richmond Sarpong, Zina Itkin, Gregory D. Cuny, Ajit Jadhav, Kyle R. Brimacombe
Publikováno v:
ACS Central Science
ACS Central Science, Vol 4, Iss 12, Pp 1727-1741 (2018)
ACS Central Science, Vol 4, Iss 12, Pp 1727-1741 (2018)
Natural products and their derivatives continue to be wellsprings of nascent therapeutic potential. However, many laboratories have limited resources for biological evaluation, leaving their previously isolated or synthesized compounds largely or com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04c15680292ccf77cdc7f1e4318e2861
http://europepmc.org/articles/PMC6311695
http://europepmc.org/articles/PMC6311695
Autor:
Elias Picazo, Daiki Kanayama, Jason V. Chari, Thomas B. Kakule, Sarah M. Anthony, K. N. Houk, Cooper S. Jamieson, Masao Ohashi, Joyann S. Barber, Dan Tan, Neil K. Garg, Yujuan Cai, Jiahai Zhou, Yi Tang, Shugeng Cao, Man-Cheng Tang
Publikováno v:
Nature, vol 586, iss 7827
Nature
Nature
An ongoing challenge in chemical research is to design catalysts that select the outcomes of the reactions of complex molecules. Chemists rely on organocatalysts or transition metal catalysts to control stereoselectivity, regioselectivity and perisel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46749750c563de0e8ad08b4d61f1c010
https://escholarship.org/uc/item/38z9m9gr
https://escholarship.org/uc/item/38z9m9gr
Publikováno v:
J Am Chem Soc
A precisely designed chiral squaramide derivative is shown to promote the highly enantioselective addition of trimethylsilyl bromide (TMSBr) to a broad variety of 3-substituted and 3,3-disubstituted oxetanes. The reaction provides direct and general
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6240720ce364489f73436a8e75b20d06
https://pubmed.ncbi.nlm.nih.gov/32364378
https://pubmed.ncbi.nlm.nih.gov/32364378
Publikováno v:
Journal of the American Chemical Society. 140:6483-6492
The akuammiline alkaloids are a structurally diverse class of bioactive natural products isolated from plants found in various parts of the world. A particularly challenging subset of akuammiline alkaloids are those that contain a methanoquinolizidin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76f70f17cd21e9d00dff87ec750b2c29
https://doi.org/10.1021/jacs.8b03404
https://doi.org/10.1021/jacs.8b03404
Publikováno v:
Synlett. 28:1-11
This account provides an overview of our laboratory’s studies of an unusual variant of the Fischer indolization reaction. We describe the discovery of the so-called ‘interrupted Fischer indolization’ and the development of the reaction from a m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7001f7ad2d6b2f764f00d616cadaf903
https://doi.org/10.1055/s-0036-1588372
https://doi.org/10.1055/s-0036-1588372
Publikováno v:
Journal of the American Chemical Society, vol 138, iss 4
The akuammiline alkaloids are a family of natural products that have been widely studied for decades. Although notable synthetic achievements have been made recently, akuammilines that possess a methanoquinolizidine core have evaded synthetic efforts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3424fe9b30c44ecf1f8a81538809cead
https://doi.org/10.1021/jacs.5b12880
https://doi.org/10.1021/jacs.5b12880
Publikováno v:
Tetrahedron letters, vol 56, iss 23
A computational study using DFT methods was performed for an array of mono and disubstituted benzynes and indolynes. The inherent distortion present in the geometry-optimized structures predicts the regioselectivity of aryne trapping by nucleophiles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36e9ba0adf84ab1ec21d759940fddef9
https://doi.org/10.1016/j.tetlet.2015.01.022
https://doi.org/10.1016/j.tetlet.2015.01.022