Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Barton, Donald"'
Autor:
Barton, Donald W.
Publikováno v:
American Journal of Botany, 1950 Oct 01. 37(8), 639-643.
Externí odkaz:
https://www.jstor.org/stable/2437875
Autor:
Barton, Donald C.
Publikováno v:
The Military Engineer, 1932 Sep 01. 24(137), 489-497.
Externí odkaz:
https://www.jstor.org/stable/44566408
Autor:
Barton, Donald C.
Publikováno v:
The Journal of Geology, 1928 Oct 01. 36(7), 615-629.
Externí odkaz:
https://www.jstor.org/stable/30059964
Autor:
Barton, Donald C.
Publikováno v:
The Journal of Geology, 1918 May 01. 26(4), 361-374.
Externí odkaz:
https://www.jstor.org/stable/30066351
Autor:
Barton, Donald C.
Publikováno v:
The Journal of Geology, 1916 May 01. 24(4), 382-393.
Externí odkaz:
https://www.jstor.org/stable/30079379
Autor:
Barton, Donald C.
Publikováno v:
The Journal of Geology, 1916 Jul 01. 24(5), 417-449.
Externí odkaz:
https://www.jstor.org/stable/30081332
Autor:
Barton, Donald C.
Publikováno v:
The Journal of Geology, 1933 Apr 01. 41(3), 225-242.
Externí odkaz:
https://www.jstor.org/stable/30058835
Autor:
Barton, Donald
Publikováno v:
The Journal of Geology, 1938 Jan 01. 46(1), 109-111.
Externí odkaz:
https://www.jstor.org/stable/30079590
Autor:
Stephen M. Stefanick, Margaret M. Lam, Seymour D. Levine, Sergio Cesco-Cancian, Charles Francis Kasulanis, Conley Richard A, Arthur C. Fabian, Barton Donald L, Stephen Currey, Gregory C. Lindabery
Publikováno v:
Journal of Heterocyclic Chemistry. 32:761-770
Several methods for the synthesis of bemarinone, 5,6-dimethoxy-4-methyl-2(1H)-quinazolinone, were explored with the most successful being a directed metalation route. Details of the lithiation and the subsequent reaction with electrophiles of 3′,4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80420d7ea61a1fdc3b65b175c19375a6
https://doi.org/10.1002/jhet.5570320312
https://doi.org/10.1002/jhet.5570320312
Publikováno v:
ChemInform. 24
The choice of base and solvent has a dramatic effect on the attack of nitrogen nucleophiles on enantiomerically enriched glycidyl sulfonates 8. Under the proper conditions attack can be largely limited to displacement of the sulfonate moiety thus ret
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d9a447dcc8755a958d00292cbf0fbdf
https://doi.org/10.1002/chin.199303065
https://doi.org/10.1002/chin.199303065