Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Matthew Del Bel"'
Autor:
Rebecca A. Gallego, Louise Bernier, Hui Chen, Sujin Cho-Schultz, Loanne Chung, Michael Collins, Matthew Del Bel, Jeff Elleraas, Cinthia Costa Jones, Ciaran N. Cronin, Martin Edwards, Xu Fang, Timothy Fisher, Mingying He, Jacqui Hoffman, Ruiduan Huo, Mehran Jalaie, Eric Johnson, Ted W. Johnson, Robert S. Kania, Manfred Kraus, Jennifer Lafontaine, Phuong Le, Tongnan Liu, Michael Maestre, Jean Matthews, Michele McTigue, Nichol Miller, Qiming Mu, Xulong Qin, Shijian Ren, Paul Richardson, Allison Rohner, Neal Sach, Li Shao, Graham Smith, Ruirui Su, Bin Sun, Sergei Timofeevski, Phuong Tran, Shuiwang Wang, Wei Wang, Ru Zhou, Jinjiang Zhu, Sajiv K. Nair
Publikováno v:
Journal of Medicinal Chemistry. 66:4888-4909
Autor:
Jin-Xin, Zhao, Yu-Xuan, Chang, Chi, He, Benjamin J, Burke, Michael R, Collins, Matthew, Del Bel, Jeff, Elleraas, Gary M, Gallego, T Patrick, Montgomery, James J, Mousseau, Sajiv K, Nair, Matthew A, Perry, Jillian E, Spangler, Julien C, Vantourout, Phil S, Baran
Publikováno v:
Proc Natl Acad Sci U S A
The development of a versatile platform for the synthesis of 1,2-difunctionalized bicyclo[1.1.1]pentanes to potentially mimic ortho/meta-substituted arenes is described. The syntheses of useful building blocks bearing alcohol, amine, and carboxylic a
Autor:
Phil S. Baran, Matthew Del Bel, Gary M. Gallego, Michael R. Collins, Matthew A. Perry, Jin-Xin Zhao, Sajiv Krishnan Nair, Yu-Xuan Chang, Benjamin J. Burke, T Patrick Montgomery, Jeff Elleraas, James J. Mousseau, Chi He, Julien C. Vantourout, Jillian E. Spangler
Publikováno v:
Proceedings of the National Academy of Sciences. 118
The development of a versatile platform for the synthesis of 1,2-difunctionalized bicyclo[1.1.1]pentanes to potentially mimic ortho/meta-substituted arenes is described. The syntheses of useful building blocks bearing alcohol, amine, and carboxylic a
Autor:
Matthew Del Bel, Jin-Xin Zhao, Sajiv Krishnan Nair, Jeff Elleraas, Michael R. Collins, JamesJ. Mousseau, Matthew A. Perry, Julien C. Vantourout, Phil S. Baran, Yu-Xuan Chang, Jillian E. Spangler, Gary M. Gallego, T Patrick Montgomery
The development of a versatile platform for the synthesis of 1,2-difunctionalized bicyclo[1.1.1]pentanes to potentially mimic ortho/meta-substituted arenes is described. The synthesis of useful building blocks bearing alcohol, amine, and carboxylic a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34fbb3e9b83f925bb8b356a84d386376
https://doi.org/10.26434/chemrxiv.13120283.v1
https://doi.org/10.26434/chemrxiv.13120283.v1
Autor:
Jinbao Xiang, Ming Shang, Yu Kawamata, Helena Lundberg, Solomon Reisberg, Miao Chen, Pavel Mykhailiuk, Gregory Beutner, Michael Collins, Alyn Davies, Matthew Del Bel, Gary Gallego, Jillian Spangler, Jeremy T. Starr, Shouliang Yang, Donna Blackmond, Phil Baran
Hindered ethers represent an underexplored area of chemical space due to the difficulty and inoperability associated with conventional reactions, despite the high-value of such structural motifs in a variety of societal applications. Demonstrated her
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ffbc16c64c698859d534d7ba2285def
https://doi.org/10.26434/chemrxiv.8144294
https://doi.org/10.26434/chemrxiv.8144294
Autor:
Helena Lundberg, Gary M. Gallego, Alyn Davies, Matthew Del Bel, Jinbao Xiang, Pavel K. Mykhailiuk, Miao Chen, Phil S. Baran, Shouliang Yang, Michael R. Collins, Jeremy T. Starr, Gregory L. Beutner, Ming Shang, Donna G. Blackmond, Solomon H. Reisberg, Yu Kawamata, Jillian E. Spangler
Publikováno v:
Nature. 573(7774)
Hindered ethers are of high value for various applications; however, they remain an underexplored area of chemical space because they are difficult to synthesize via conventional reactions1,2. Such motifs are highly coveted in medicinal chemistry, be
Publikováno v:
Journal of the American Chemical Society. 139(20)
Herein we describe concise enantioselective chemical syntheses of (−)-viridin and (−)-viridiol. Our convergent approach couples two achiral fragments of similar complexity and employs an enantioselective intramolecular Heck reaction to set the ab
Autor:
Phil S. Baran, Matthew Del Bel, Ryan Gianatassio, Yuta Fujiwara, Victoriano Domingo, Ian B. Seiple
Publikováno v:
Journal of the American Chemical Society. 133:3292-3295
A direct functionalization of a variety of quinones with several boronic acids has been developed. This scalable reaction proceeds readily at room temperature in an open flask using inexpensive reagents: catalytic silver(I) nitrate in the presence of
Publikováno v:
ChemInform. 45
Herein, we describe a two-step method for the cyclopentannulation of conjugated enones using methyl 3-(tert-butyldimethylsilyloxy)-2-diazo-3-butenoate (1) as a bifunctional reagent. The enol silane and stabilized diazoalkane functionalities are explo
Publikováno v:
Journal of the American Chemical Society. 135(33)
Herein, we describe a two-step method for the cyclopentannulation of conjugated enones using methyl 3-(tert-butyldimethylsilyloxy)-2-diazo-3-butenoate (1) as a bifunctional reagent. The enol silane and stabilized diazoalkane functionalities are explo