Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Thomas D. Caputo"'
Publikováno v:
Tetrahedron. 56:2397-2401
A highly stereoselective method for the synthesis of (E)-β-halogeno Baylis–Hillman adducts has been developed. The new method involves a tandem α-hydroxyalkylation/β-chlorination of α,β-acetylenic ketones by using TiCl4 as the chlorine source
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ccadfc929e5994de420b9eff81440c4
https://doi.org/10.1016/s0040-4020(00)00151-4
https://doi.org/10.1016/s0040-4020(00)00151-4
Publikováno v:
Tetrahedron Letters. 41:1-5
TiCl4-Mediated Baylis–Hillman and aldol reactions were developed without the direct use of a Lewis base. These processes involve the conjugate addition of TiCl4 to α,β-unsaturated substrates followed by carbonyl coupling. Baylis–Hillman olefins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfbb064cb1262c63c97f3b6eac7a7ef9
https://doi.org/10.1016/s0040-4039(99)01992-9
https://doi.org/10.1016/s0040-4039(99)01992-9
Autor:
Jeffrey A. Rossmann, David G. Kerns, Garth R. Griffiths, James B. Barnes, Michael A. E. Ramsay, Thomas D. Caputo, M. Miles Beach, Paul Ezzo, Brad Crump, Benjamin Meyrat, Barnett Bookatz
Publikováno v:
Proceedings (Baylor University. Medical Center). 24(3)
Brain function monitors have improved safety and efficiency in general anesthesia; however, they have not been adequately tested for guiding conscious sedation for periodontal surgical procedures. This study evaluated the patient state index (PSI) ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ecaa607cbe65ee416af4b9154863baf
https://pubmed.ncbi.nlm.nih.gov/21738291
https://pubmed.ncbi.nlm.nih.gov/21738291
Publikováno v:
ChemInform. 31
TiCl4-Mediated Baylis–Hillman and aldol reactions were developed without the direct use of a Lewis base. These processes involve the conjugate addition of TiCl4 to α,β-unsaturated substrates followed by carbonyl coupling. Baylis–Hillman olefins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2f31be8040fd635cb557db96828254e
https://doi.org/10.1002/chin.200010083
https://doi.org/10.1002/chin.200010083
Publikováno v:
ChemInform. 31
A highly stereoselective method for the synthesis of (E)-β-halogeno Baylis–Hillman adducts has been developed. The new method involves a tandem α-hydroxyalkylation/β-chlorination of α,β-acetylenic ketones by using TiCl4 as the chlorine source
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40a5914f1cb2d53a057e0e432223fa3a
https://doi.org/10.1002/chin.200030044
https://doi.org/10.1002/chin.200030044