Thomson, Jennifer E.; Kyle, Andrew F.; Ling, Kenneth B.; Smith, Siobhan R.; Slawin, Alexandra M. Z.; Smith, Andrew D. published the artcile< Applications of NHC-mediated O- to C-carboxyl transfer: synthesis of (±)-N-benzyl-coerulescine and (±)-horsfiline>, Recommanded Product: (9Z,12Z)-Methyl octadeca-9,12-dienoate, the main research area is coerulescine horsfiline oxindole alkaloid synthesis carboxyl transfer rearrangement.
N-Heterocyclic carbene (NHC) promoted O- to C-carboxyl transfer of 3-allylindolyl Ph carbonates generated 3-allyl-3-phenoxycarbonyloxindoles with good catalytic efficiency, which were readily converted into (±)-N-benzylcoerulescine (I) and (±)-horsfiline (II).
Tetrahedron published new progress about Oxindole alkaloids Role: SPN (Synthetic Preparation), PREP (Preparation). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Recommanded Product: (9Z,12Z)-Methyl octadeca-9,12-dienoate.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics