Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mary K. Balmer"'
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[563-63-3] C2H3AgO2 (MW 166.92) InChI = 1S/C2H4O2.Ag/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1 InChIKey = CQLFBEKRDQMJLZ-UHFFFAOYSA-M (nucleophilic substitutions;5 cyclizations;1 couplings;14 disulfide cleavage13) Alternate Names: silver acetate; silver monoa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cc6152004301c05fec532799f99d481
https://doi.org/10.1002/047084289x.rs013m.pub3
https://doi.org/10.1002/047084289x.rs013m.pub3
Autor:
Thomas Albert, and Mary K. Balmer, Lee A. Reif, David P. Sawick, Hemantkumar H. Patel, Ramesh R. Patel, Sanjay R. Chemburkar, Bhadra Shelat
Publikováno v:
Organic Process Research & Development. 1:294-299
The evolution and development of a commercially viable synthesis of fenleuton, a second-generation 5-lipoxygenase inhibitor, is discussed. Special emphasis is given to the challenges and operational issues encountered on scale-up in the pilot plant.
Publikováno v:
Tetrahedron. 51:11043-11062
A method has been developed which allows for the large scale preparation of biarylmethanes This method involves the initial formation of biarylmethanols via reaction of aryl Grignards with carbonyl compounds followed by a subsequent reduction with io
Publikováno v:
ChemInform. 27
A method has been developed which allows for the large scale preparation of biarylmethanes This method involves the initial formation of biarylmethanols via reaction of aryl Grignards with carbonyl compounds followed by a subsequent reduction with io