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S Baran

Showing results (111-120 of 348) with videos related to

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The Journal of Organic Chemistry|March 20, 2023
Small Change, Big Impact: Reversal of Diastereoselection in Cuprate Conjugate Additions to α,β-Unsaturated Lactams and Identification of a Competing MechanismStephen W Wright, Chulho Choi, Yu Kawamata, et al.
Angewandte Chemie (International Ed. in English)|July 4, 2001
Rapid Access to Complex Molecular Architectures via o-Azaquinones We thank Dr. D. H. Huang, G. Siuzdak, and Dr. R. Chadha for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. This work was supported financially by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from the National Science Foundation (P.S.B), and grants from ArrayBiopharma, Pfizer, Glaxo, Merck, Schering Plough, Hoffmann-La Roche, Boehringer Ingelheim, DuPont, and Abbott LaboratoriesK. C. Nicolaou, Yong-Li Zhong, Phil S. Baran, et al.
Angewandte Chemie (International Ed. in English)|May 16, 2001
New Synthetic Technology for the Construction of N-Containing Quinones and Derivatives Thereof: Total Synthesis of Epoxyquinomycin B We thank Dr. D. H. Huang, Dr. G. Siuzdak, and Dr. R. Chadha for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from the National Science Foundation (P.B.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering PloughK. C. Nicolaou, Kazuyuki Sugita, Phil S. Baran, et al.
The Journal of Antibiotics|October 7, 2010
The psychotrimine natural products have antibacterial activity against Gram-positive bacteria and act via membrane disruptionMark A Schallenberger, Timothy Newhouse, Phil S Baran, et al.
Journal of the American Chemical Society|December 4, 2008
Total syntheses of (+/-)-massadine and massadine chlorideShun Su, Ian B Seiple, Ian S Young, et al.
Journal of the American Chemical Society|September 16, 2016
Radicals: Reactive Intermediates with Translational PotentialMing Yan, Julian C Lo, Jacob T Edwards, et al.
Journal of Medicinal Chemistry|February 1, 1974
Synthesis and biological activities of substituted glycyrrhetic acidsJ S Baran, D D Langford, C Liang, et al.
Journal of the American Chemical Society|April 28, 2020
Total Synthesis of (-)-MaximiscinKyle S McClymont, Feng-Yuan Wang, Amin Minakar, et al.
Angewandte Chemie (International Ed. in English)|February 13, 2001
New Synthetic Technology for the Construction of N-Containing Quinones and Derivatives Thereof: Total Synthesis of Epoxyquinomycin B We thank Dr. D. H. Huang, Dr. G. Siuzdak, and Dr. R. Chadha for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from the National Science Foundation (P.B.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering PloughK. C. Nicolaou, Kazuyuki Sugita, Phil S. Baran, et al.
Organic Letters|September 20, 2011
Practical radical cyclizations with arylboronic acids and trifluoroboratesJonathan W Lockner, Darryl D Dixon, Rune Risgaard, et al.
Pageof 35

Showing results (111-120 of 348) with videos related to

Sort By:
Pageof 35
The Journal of Organic Chemistry|March 20, 2023
Small Change, Big Impact: Reversal of Diastereoselection in Cuprate Conjugate Additions to α,β-Unsaturated Lactams and Identification of a Competing MechanismStephen W Wright, Chulho Choi, Yu Kawamata, et al.
Angewandte Chemie (International Ed. in English)|July 4, 2001
Rapid Access to Complex Molecular Architectures via o-Azaquinones We thank Dr. D. H. Huang, G. Siuzdak, and Dr. R. Chadha for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. This work was supported financially by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from the National Science Foundation (P.S.B), and grants from ArrayBiopharma, Pfizer, Glaxo, Merck, Schering Plough, Hoffmann-La Roche, Boehringer Ingelheim, DuPont, and Abbott LaboratoriesK. C. Nicolaou, Yong-Li Zhong, Phil S. Baran, et al.
Angewandte Chemie (International Ed. in English)|May 16, 2001
New Synthetic Technology for the Construction of N-Containing Quinones and Derivatives Thereof: Total Synthesis of Epoxyquinomycin B We thank Dr. D. H. Huang, Dr. G. Siuzdak, and Dr. R. Chadha for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from the National Science Foundation (P.B.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering PloughK. C. Nicolaou, Kazuyuki Sugita, Phil S. Baran, et al.
The Journal of Antibiotics|October 7, 2010
The psychotrimine natural products have antibacterial activity against Gram-positive bacteria and act via membrane disruptionMark A Schallenberger, Timothy Newhouse, Phil S Baran, et al.
Journal of the American Chemical Society|December 4, 2008
Total syntheses of (+/-)-massadine and massadine chlorideShun Su, Ian B Seiple, Ian S Young, et al.
Journal of the American Chemical Society|September 16, 2016
Radicals: Reactive Intermediates with Translational PotentialMing Yan, Julian C Lo, Jacob T Edwards, et al.
Journal of Medicinal Chemistry|February 1, 1974
Synthesis and biological activities of substituted glycyrrhetic acidsJ S Baran, D D Langford, C Liang, et al.
Journal of the American Chemical Society|April 28, 2020
Total Synthesis of (-)-MaximiscinKyle S McClymont, Feng-Yuan Wang, Amin Minakar, et al.
Angewandte Chemie (International Ed. in English)|February 13, 2001
New Synthetic Technology for the Construction of N-Containing Quinones and Derivatives Thereof: Total Synthesis of Epoxyquinomycin B We thank Dr. D. H. Huang, Dr. G. Siuzdak, and Dr. R. Chadha for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from the National Science Foundation (P.B.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering PloughK. C. Nicolaou, Kazuyuki Sugita, Phil S. Baran, et al.
Organic Letters|September 20, 2011
Practical radical cyclizations with arylboronic acids and trifluoroboratesJonathan W Lockner, Darryl D Dixon, Rune Risgaard, et al.
Pageof 35