Zobrazeno 1 - 10
of 12
pro vyhledávání: '"K. E. Starbuck"'
Publikováno v:
Tetrahedron Letters. 37:4113-4116
By using a benzyl copper reagent (e.g. 10→11) in combination with titanium enolate chemistry (e.g. 12→13) a concise sequence has been developed for the rapid introduction of functionality found in the cytochalasin HIV protease inhibitor (1).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::460b8bb9d84816237bca328f4627e13f
https://doi.org/10.1016/0040-4039(96)00778-2
https://doi.org/10.1016/0040-4039(96)00778-2
Publikováno v:
ChemInform. 23
Versatile and concise routes to both racemic and chiral cyclopentane analogs of valinol are described. These compounds are constrained analogs of a key amino acid found in the aspartyl protease inhibitors of HIV-1.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a50e4363027c34047f4e4a3dbc314d98
https://doi.org/10.1002/chin.199229122
https://doi.org/10.1002/chin.199229122
Publikováno v:
ChemInform. 27
By using a benzyl copper reagent (e.g. 10→11) in combination with titanium enolate chemistry (e.g. 12→13) a concise sequence has been developed for the rapid introduction of functionality found in the cytochalasin HIV protease inhibitor (1).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb12a1eee36b37f337b901dc3e41dc8d
https://doi.org/10.1002/chin.199637171
https://doi.org/10.1002/chin.199637171
Publikováno v:
Tetrahedron Letters. 32:6851-6854
Versatile and concise routes to both racemic and chiral cyclopentane analogs of valinol are described. These compounds are constrained analogs of a key amino acid found in the aspartyl protease inhibitors of HIV-1.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ba8faca58c0dc697db39918089d2586
https://doi.org/10.1016/0040-4039(91)80423-4
https://doi.org/10.1016/0040-4039(91)80423-4
Autor:
Cheng YY; Wöhler Research Institute for Sustainable Chemistry (WISCh), Georg-August-Universität Göttingen, Tammannstraße 2, Göttingen, 37077, Germany., Xu J; Wöhler Research Institute for Sustainable Chemistry (WISCh), Georg-August-Universität Göttingen, Tammannstraße 2, Göttingen, 37077, Germany., Lin Z; Wöhler Research Institute for Sustainable Chemistry (WISCh), Georg-August-Universität Göttingen, Tammannstraße 2, Göttingen, 37077, Germany., Li Y; Wöhler Research Institute for Sustainable Chemistry (WISCh), Georg-August-Universität Göttingen, Tammannstraße 2, Göttingen, 37077, Germany., Ackermann L; Wöhler Research Institute for Sustainable Chemistry (WISCh), Georg-August-Universität Göttingen, Tammannstraße 2, Göttingen, 37077, Germany.
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2024 Oct 23; Vol. 30 (59), pp. e202402333. Date of Electronic Publication: 2024 Oct 07.
Publikováno v:
Greene's Protective Groups in Organic Synthesis (9781118057483); 2014, p895-1193, 299p
Autor:
Wuts, Peter G. M., Greene, Theodora W.
Publikováno v:
Greene's Protective Groups in Organic Synthesis; 2006, p696-926, 231p
This is the eBook of the printed book and may not include any media, website access codes, or print supplements that may come packaged with the bound book. Presents Social Gerontology from Multiple Perspectives Aging Matters illuminates cultural, bio
Autor:
Peter G. M. Wuts
An indispensable reference for any practicing synthetic organic or medicinal chemist, this book continues the tradition of Greene's as comprehensive in the overall scope of coverage, providing the most relevant and useful examples to illustrate each
Autor:
Peter G. M. Wuts, Theodora W. Greene
The Fourth Edition of Greene's Protective Groups in Organic Synthesis continues to be an indispensable reference for controlling the reactivity of the most common functional groups during a synthetic sequence. This new edition incorporates the signif