Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ronan le Vezouet"'
Autor:
Aaron D. Gross, Yoshihisa Ozoe, Joel R. Coats, Jennina Taylor-Wells, Andrew K. Jones, Toshifumi Nakao, Keiji Tanaka, Takaaki Sakamoto, Takaaki Iwai, Kou Kuroda, Karin Nagasaki, Miki Akamatsu, Kazuhiko Matsuda, Shruti Sharan, Catherine A. Hill, S. Blankenburg, S. Balfanz, A. Baumann, W. Blenau, Hiroto Ohta, Kanako Mitsumasu, Toshinobu Yaginuma, Yoshiaki Tanaka, Kiyoshi Asaoka, Jia Huang, Barbara Wedel, Wolfgang von Deyn, Sebastian Soergel, Matthias Pohlman, Douglas Anspaugh, Ramani Kandasamy, Fae Malone, Daniel Houtz, Nancy Rankl, John Dorsch, Lynn Stam, Brecht London, Ronan le Vezouet, Christopher Koradin, Markus Kordes
Autor:
Matthias Pohlman, Markus Kordes, Houtz Daniel, Lynn Stam, Wolfgang von Deyn, Sebastian Soergel, Douglas D. Anspaugh, Ramani A. Kandasamy, Brecht London, Christopher Koradin, Nancy B. Rankl, Malone Fae, Ronan le Vezouet, Barbara J. Wedel, Dorsch John
Publikováno v:
ACS Symposium Series ISBN: 9780841232600
ACS Symposium Series
ACS Symposium Series
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19649bc2c5d73931d95ff1b1b88b307c
https://doi.org/10.1021/bk-2017-1265.ch008
https://doi.org/10.1021/bk-2017-1265.ch008
Autor:
Andrew J. P. White, Ronan Le Vezouet, Aleksandra Siwicka, Livio Tedeschi, Anthony G. M. Barrett, David Cuperly
Publikováno v:
Tetrahedron. 63:5903-5917
A concise and efficient synthesis of the C 13 tricyclic core of the dihydro-β-agarofuran skeleton common to the natural Celastraceae sesquiterpenoids is described. The strategy entails a Mukaiyama aldol reaction of a tetrahydronaphthalene enol silan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82f3131e0f2773d57c51dcefecbe2683
https://doi.org/10.1016/j.tet.2007.02.021
https://doi.org/10.1016/j.tet.2007.02.021
Publikováno v:
Tetrahedron. 62:12252-12263
Both (1) furan–maleimide Diels–Alder cycloaddition reaction and (2) furan–benzyne cycloaddition, Suzuki cross-coupling, boron-mediated aldol, and electrophilic aromatic substitution reactions were examined for the construction of the CDEF ring
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14deea69528a26e3fd0abd595f71bfa2
https://doi.org/10.1016/j.tet.2006.10.004
https://doi.org/10.1016/j.tet.2006.10.004
Autor:
Peter W. Seale, Richard J. Upton, David J. Williams, Stefan Stefaniak, and Andrew J. P. White, Panayiotis Alexandrou Procopiou, Anthony G. M. Barrett, Alan Joseph Hennessy, Ronan Le Vezouet
Publikováno v:
The Journal of Organic Chemistry. 69:1028-1037
The synthesis of a range of highly functionalized peptidomimetic macrocycles has been accomplished using ring-closing metathesis and enyne tandem cross-metathesis-ring-closing metathesis reactions. This approach gives access to rigidified macrocycles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::806e69f0f131596c0844f8dd57751de7
https://doi.org/10.1021/jo0352629
https://doi.org/10.1021/jo0352629