Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Benjamin D. Sherry"'
Autor:
Ben W. H. Turnbull, Feng Peng, Andrew J. Neel, Tamas Benkovics, Zhuqing Liu, Cheol K. Chung, Zhiguo Jake Song, Lushi Tan, Khateeta M. Emerson, Chengqian Xiao, Yi Zhang, Benjamin D. Sherry
Publikováno v:
Organic Process Research & Development. 27:448-457
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33ab1b411fa50fe0ce8e4fbc7655b708
https://doi.org/10.1021/acs.oprd.2c00397
https://doi.org/10.1021/acs.oprd.2c00397
Autor:
Tamas Benkovics, Feng Peng, Eric M. Phillips, Chihui An, Rachel S. Bade, Cheol K. Chung, Zachary E. X. Dance, Patrick S. Fier, Jacob H. Forstater, Zhijian Liu, Zhuqing Liu, Peter E. Maligres, Nicholas M. Marshall, Nastaran Salehi Marzijarani, John A. McIntosh, Steven P. Miller, Jeffrey C. Moore, Andrew J. Neel, Jennifer V. Obligacion, Weilan Pan, Michael T. Pirnot, Marc Poirier, Mikhail Reibarkh, Benjamin D. Sherry, Zhiguo Jake Song, Lushi Tan, Ben W. H. Turnbull, Deeptak Verma, Jacob H. Waldman, Lu Wang, Tao Wang, Matthew S. Winston, Feng Xu
Publikováno v:
Journal of the American Chemical Society. 144:5855-5863
As practitioners of organic chemistry strive to deliver efficient syntheses of the most complex natural products and drug candidates, further innovations in synthetic strategies are required to facilitate their efficient construction. These aspiratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2857eb6c7a9763b83124f43fd6446213
https://doi.org/10.1021/jacs.1c12106
https://doi.org/10.1021/jacs.1c12106
Autor:
Feiyue Wu, Adam J. Fine, Jungchul Kim, Feng Peng, Anna V. Jenks, Khateeta M. Emerson, Benjamin D. Sherry, Marco Euclide Armenante, Roman Kats-Kagan, Anil R. Ekkati, Feng Xu, Tetsuji Itoh, Andrew Brunskill, Zachary E. X. Dance, Zhijian Liu, Debra J. Wallace, Jacob H. Waldman, Jennifer V. Obligacion, Patrick S. Fier
Publikováno v:
Organic Process Research & Development. 25:2249-2259
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18959ed2cbfceb5c2111d431508e88f5
https://doi.org/10.1021/acs.oprd.1c00149
https://doi.org/10.1021/acs.oprd.1c00149
Autor:
John A. McIntosh, Zhijian Liu, Brian M. Andresen, Nastaran Salehi Marzijarani, Jeffrey C. Moore, Nicholas M. Marshall, Margie Borra-Garske, Jennifer V. Obligacion, Patrick S. Fier, Feng Peng, Jacob H. Forstater, Matthew S. Winston, Chihui An, Wonsuk Chang, Jongwon Lim, Mark A. Huffman, Steven P. Miller, Fuh-Rong Tsay, Michael D. Altman, Charles A. Lesburg, Dietrich Steinhuebel, B. Wesley Trotter, Jared N. Cumming, Alan Northrup, Xiaodong Bu, Benjamin F. Mann, Mirlinda Biba, Kaori Hiraga, Grant S. Murphy, Joshua N. Kolev, Amanda Makarewicz, Weilan Pan, Iman Farasat, Rachel S. Bade, Kevin Stone, Da Duan, Oscar Alvizo, Donovan Adpressa, Erik Guetschow, Erik Hoyt, Erik L. Regalado, Steve Castro, Nelo Rivera, Joseph P. Smith, Fengqiang Wang, Alejandro Crespo, Deeptak Verma, Stephanus Axnanda, Zachary E. X. Dance, Paul N. Devine, David Tschaen, Keith A. Canada, Paul G. Bulger, Benjamin D. Sherry, Matthew D. Truppo, Rebecca T. Ruck, Louis-Charles Campeau, David Jonathan Bennett, Guy R. Humphrey, Kevin R. Campos, Matthew L. Maddess
Publikováno v:
Nature. 603(7901)
The introduction of molecular complexity in an atom- and step-efficient manner remains an outstanding goal in modern synthetic chemistry. Artificial biosynthetic pathways are uniquely able to address this challenge by using enzymes to carry out multi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33a99659551d71437d1bb960c572370b
https://pubmed.ncbi.nlm.nih.gov/35296845
https://pubmed.ncbi.nlm.nih.gov/35296845
Autor:
Zhiyan Song, Nastaran Salehi Marzijarani, Yining Ji, Ji Qi, Yu-hong Lam, Benjamin D. Sherry, Artis Klapars, Xiao Wang, Zhijian Liu
Publikováno v:
Journal of the American Chemical Society. 142(47)
An efficient synthesis of nucleoside 5'-monothiophosphates under mild reaction conditions using commercially available thiophosphoryl chloride was achieved with a cinchona alkaloid catalyst. A detailed mechanistic study of the reaction was undertaken
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ecb9800e39a40f45c301272e8fa9f38
https://pubmed.ncbi.nlm.nih.gov/33180475
https://pubmed.ncbi.nlm.nih.gov/33180475
Publikováno v:
ACS Symposium Series ISBN: 9780841298644
ACS Symposium Series
ACS Symposium Series
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::157f089803e52e76573c057948c3fa44
https://doi.org/10.1021/bk-2020-1369.ch008
https://doi.org/10.1021/bk-2020-1369.ch008
Autor:
Benjamin D. Sherry, Joseph Kukura, Jonathan P. McMullen, Glenn Spencer, Christopher H. Marton, Natalie S. Eyke
Publikováno v:
Organic Process Research & Development. 22:1208-1213
Examples of continuous flow reactions in the laboratory setting are becoming commonplace in pharmaceutical drug substance research. Developing these processes for robust commercialization and ident...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a16c61d4faaafab7a577fd1d3f3a75f
https://doi.org/10.1021/acs.oprd.8b00192
https://doi.org/10.1021/acs.oprd.8b00192
Autor:
Benjamin D. Sherry, Nobuyoshi Yasuda, Mark Weisel, Yining Ji, Feng Xu, Debra J. Wallace, Jinchu Liu, Jianguo Yin, Zhijian Liu
Publikováno v:
Organic Process Research & Development. 22:273-277
Previous methods to prepare a bicyclic N-hydroxyl urea intermediate in the synthesis of the potent β-lactamase inhibitor relebactam were effective, but deemed unsuitable for long-term use. Therefore, we developed an in situ protection protocol durin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c5bb8ae70b2df359c104f045b7ed527
https://doi.org/10.1021/acs.oprd.7b00381
https://doi.org/10.1021/acs.oprd.7b00381
Autor:
Danielle M. Schultz, Benjamin D. Sherry, Huaming Sheng, François Lévesque, Ian W. Davies, James F. Dropinski, Leo A. Joyce, Yining Ji, Daniel A. DiRocco, Mikhail Reibarkh
Publikováno v:
Angewandte Chemie (International ed. in English). 56(48)
Aliphatic amines, oxygenated at remote positions within the molecule, represent an important class of synthetic building blocks to which there are currently no direct means of access. Reported herein is an efficient and scalable solution that relies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d29f0a3fad9ff921657812dfe8544ab
https://pubmed.ncbi.nlm.nih.gov/29044797
https://pubmed.ncbi.nlm.nih.gov/29044797
Autor:
Ahmed F. Abdel-Magid, Jaan A. Pesti, Rajappa Vaidyanathan, Debra J. Wallace, Ian Mangion, Paul Coleman, Seb Caille, John G. Allen, Xianglin Shi, William F. Kiesman, Donald G. Walker, Hidenori Takahashi, Alessandra Bartolozzi, Thomas Simpson, Keith Fandrick, Jason Mulder, Jean-Nicolas Desrosiers, Nitin Patel, Xingzhong Zeng, Daniel Fandrick, Carl A. Busacca, Jinhua J. Song, Chris H. Senanayake, Timothy P. Heffron, Andrew McClory, Andreas Stumpf, Jason D. Burch, Benjamin D. Sherry, Donald R. Gauthier, Louis-Charles Campeau, Jessica E. Reed, Jeff B. Smaill, Shu Yu, Olivier Dirat, Jed L. Hubbs, Nathan O. Fuller, Wesley F. Austin, Ruichao Shen, Brian S. Bronk, Gerald J. Tanoury, Stephen Eastham, Cristian L. Harrison, Benjamin J. Littler, Piero L. Ruggiero, Zhifeng Ye, Anne-Laure Grillo