367954-21-0Relevant articles and documents
Palladium Catalyzed Stereoselective Arylation of Biocatalytically Derived Cyclic 1,3-Dienes: Chirality Transfer via a Heck-Type Mechanism
Dun?s, Petter,Kann, Nina,Kociok-K?hn, Gabriele,Lewis, Simon E.,Norrby, Per-Ola,Paterson, Andrew J.,Rahm, Martin
supporting information, p. 2464 - 2469 (2020/08/05)
Microbial arene oxidation of benzoic acid with Ralstonia eutropha B9 provides a chiral highly functionalized cyclohexadiene, suitable for further structural diversification. Subjecting this scaffold to a Pd-catalyzed Heck reaction effects a regio-and ster
Synthesis of a broad array of highly functionalized, enantiomerically pure cyclohexanecarboxylic acid derivatives by microbial dihydroxylation of benzoic acid and subsequent oxidative and rearrangement reactions
Myers, Andrew G.,Siegel, Dionicio R.,Buzard, Daniel J.,Charest, Mark G.
, p. 2923 - 2926 (2007/10/03)
(equation presented) We have found that the 1,2-dihydroxylation of benzoic acid with Alcaligenes eutrophus strain B9, first reported in 1971 by Reiner and Hegeman, is readily adapted for the preparation of tens to hundreds of grams of (1S,2R)-1,2-dihydrox