Zobrazeno 1 - 8
of 8
pro vyhledávání: '"John A. Colapret"'
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[78-94-4] C4H6O (MW 70.10) [59120-04-6] InChI = 1S/C4H6O/c1-3-4(2)5/h3H,1H2,2H3 InChIKey = FUSUHKVFWTUUBE-UHFFFAOYSA-N InChI = 1/C4H6O/c1-3-4(2)5/h3H,1H2,2H3 InChIKey = FUSUHKVFWTUUBE-UHFFFAOYAV (reagent for attachment of 3-oxobutyl side chains, i.e.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1315a9ad93aec01caa4943b76bbb5198
https://doi.org/10.1002/047084289x.rm276.pub2
https://doi.org/10.1002/047084289x.rm276.pub2
Autor:
Mark J. Benvenga, Richard L Wynn, John A. Colapret, Michael H. Ossipov, Theodore C. Spaulding, Nhora Lucia Lalinde, Frieda G. Rudo, Jerome R. Bagley, Bao-Shang Huang, Bor-Sheng Lin, Thomas P. Jerussi, Linas V. Kudzma, Brian M. Doorley, Spencer H Kenneth
Publikováno v:
Medicinal research reviews. 11(4)
The findings reviewed herein have been the results of a five-year project undertaken by Anaquest to discover new therapeutically superior analgesics. The need to provide an analgesic for severe to moderate pain in the perioperative and nonsurgical en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df53c38c2f926282b72a17017699d966
https://pubmed.ncbi.nlm.nih.gov/1875771
https://pubmed.ncbi.nlm.nih.gov/1875771
Publikováno v:
The Journal of Organic Chemistry. 54:2209-2216
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48f85c8960df080b5fb6d47d493392da
https://doi.org/10.1021/jo00270a035
https://doi.org/10.1021/jo00270a035
Publikováno v:
The Journal of Organic Chemistry. 44:3391-3396
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c0fd4000d3914e0da7a8bd0550aa098
https://doi.org/10.1021/jo01333a025
https://doi.org/10.1021/jo01333a025
Publikováno v:
Journal of the American Chemical Society. 102:5866-5872
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a07a1bd9bc251e1443571297efef252
https://doi.org/10.1021/ja00538a027
https://doi.org/10.1021/ja00538a027
Publikováno v:
The Journal of Organic Chemistry. 50:201-205
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa1dd6b3ca744643ab44dae55d023838
https://doi.org/10.1021/jo00202a012
https://doi.org/10.1021/jo00202a012
Publikováno v:
Chemischer Informationsdienst. 16
Par transposition oxyanionique de Cope, l'addition du cyclopentene-1yl lithium avec les methyl-7 vinyl-7 bicyclo [3.2.0] heptene-2ones-6(7R) conduit aux derives du dicyclopenta [a,d] cyclooctane tout cis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::457f42c95e090baa8eb132f3c1d4d7b3
https://doi.org/10.1002/chin.198526158
https://doi.org/10.1002/chin.198526158