On May 1, 2020, Popadynec, Michael; Gibbard, Helen; Clark, J. Stephen published an article.Related Products of 2873-29-2 The title of the article was Bidirectional Synthesis of the IJK Fragment of Ciguatoxin CTX3C by Sequential Double Ring-Closing Metathesis and Tsuji-Trost Allylation. And the article contained the following:
A novel four-step bidirectional strategy has been used to synthesize the IJK fragment (I) of the marine polyether natural product CTX3C from a simple monocyclic precursor in a concise and efficient manner. The four-step bidirectional sequence involves ring-closing metathesis, alc. oxidation, enol carbonate formation, and palladium-mediated Tsuji-Trost allylation. The experimental process involved the reaction of (2R,3S,4R)-2-(Acetoxymethyl)-3,4-dihydro-2H-pyran-3,4-diyl diacetate(cas: 2873-29-2).Related Products of 2873-29-2
The Article related to ring closing metathesis oxidation palladium tsuji trost allylation diastereoselective, ciguatoxin ijk fragment stereoselective preparation, Biomolecules and Their Synthetic Analogs: Others, Including Purines, Pyrimidine Nucleic Acid Bases, Flavins, Lignans and other aspects.Related Products of 2873-29-2
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Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics