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Ken Yoshioka

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European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|June 4, 2026
A Structure-Derived Compositional Framework for Interpreting Membrane Permeability via Relative Interaction BalanceKen Yoshioka
Nature Communications|March 21, 2017
Complete diastereodivergence in asymmetric 1,6-addition reactions enabled by minimal modification of a chiral catalystDaisuke Uraguchi, Ken Yoshioka, Takashi Ooi
Chemical Communications (Cambridge, England)|May 5, 2017
Unique site-selectivity control in asymmetric Michael addition of azlactone to alkenyl dienyl ketones enabled by P-spiro chiral iminophosphorane catalysisKen Yoshioka, Kohei Yamada, Daisuke Uraguchi, et al.
Journal of the American Chemical Society|November 14, 2012
Highly regio-, diastereo-, and enantioselective 1,6- and 1,8-additions of azlactones to di- and trienyl N-acylpyrrolesDaisuke Uraguchi, Ken Yoshioka, Yusuke Ueki, et al.
Bioscience, Biotechnology, and Biochemistry|October 8, 2008
Efficient synthesis of a new L-shaped dimer of naphthalene, and its analogsKen Yoshioka, Izumi Takaishi, Kazunari Shiozawa, et al.
The Journal of Organic Chemistry|December 21, 2016
Origin of High Regio-, Diastereo-, and Enantioselectivities in 1,6-Addition of Azlactones to Dienyl N-Acylpyrroles: A Computational StudyMasahiro Yamanaka, Ken Sakata, Ken Yoshioka, et al.
Angewandte Chemie (International Ed. in English)|February 14, 2018
Catalyst-Enabled Site-Divergent Stereoselective Michael Reactions: Overriding Intrinsic Reactivity of Enynyl Carbonyl AcceptorsDaisuke Uraguchi, Ryo Shibazaki, Naoya Tanaka, et al.
Chemical & Pharmaceutical Bulletin|May 9, 2003
Analysis of the peptides (Prp106-126, MSI-78A, and Oxaldie 1) with the same biological activity by discrete Fourier transform: toward a selection rule in ligand-receptor interactionNaganori Numao, Hisashi Fujii, Yoshiyuki Fukazawa, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|June 4, 2026
A Structure-Derived Compositional Framework for Interpreting Membrane Permeability via Relative Interaction BalanceKen Yoshioka
Nature Communications|March 21, 2017
Complete diastereodivergence in asymmetric 1,6-addition reactions enabled by minimal modification of a chiral catalystDaisuke Uraguchi, Ken Yoshioka, Takashi Ooi
Chemical Communications (Cambridge, England)|May 5, 2017
Unique site-selectivity control in asymmetric Michael addition of azlactone to alkenyl dienyl ketones enabled by P-spiro chiral iminophosphorane catalysisKen Yoshioka, Kohei Yamada, Daisuke Uraguchi, et al.
Journal of the American Chemical Society|November 14, 2012
Highly regio-, diastereo-, and enantioselective 1,6- and 1,8-additions of azlactones to di- and trienyl N-acylpyrrolesDaisuke Uraguchi, Ken Yoshioka, Yusuke Ueki, et al.
Bioscience, Biotechnology, and Biochemistry|October 8, 2008
Efficient synthesis of a new L-shaped dimer of naphthalene, and its analogsKen Yoshioka, Izumi Takaishi, Kazunari Shiozawa, et al.
The Journal of Organic Chemistry|December 21, 2016
Origin of High Regio-, Diastereo-, and Enantioselectivities in 1,6-Addition of Azlactones to Dienyl N-Acylpyrroles: A Computational StudyMasahiro Yamanaka, Ken Sakata, Ken Yoshioka, et al.
Angewandte Chemie (International Ed. in English)|February 14, 2018
Catalyst-Enabled Site-Divergent Stereoselective Michael Reactions: Overriding Intrinsic Reactivity of Enynyl Carbonyl AcceptorsDaisuke Uraguchi, Ryo Shibazaki, Naoya Tanaka, et al.
Chemical & Pharmaceutical Bulletin|May 9, 2003
Analysis of the peptides (Prp106-126, MSI-78A, and Oxaldie 1) with the same biological activity by discrete Fourier transform: toward a selection rule in ligand-receptor interactionNaganori Numao, Hisashi Fujii, Yoshiyuki Fukazawa, et al.
Pageof 1