The Journal of Organic Chemistry · 2007 · 44 citations · 43 references
Natural SciencesChemistryMedicinal ChemistryOrganic ChemistryGlycosidic Bond FormationOrganic SynthesisRetrosynthetic AnalysisCross CouplingGlycoside SynthesisGlycosidic Bond StereochemistryGlycosylation StereochemistryHydroboration Of AlkynesReaction CouplingStereoselective GlycosylationSuzuki - Miyaura Coupling
A synthesis of the C(1)-C(11) fragment of apoptolidin A has been accomplished by a convergent route involving the stereoselective glycosidation of 9 and the Suzuki cross-coupling reaction of bromodienoate 7 and the vinylborane generated via chemoselective hydroboration of diyne 6 with diisopinocampheylborane.
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N-methoxy-n-methylamides as effective acylating agents
Steven Nahm, Steven M. Weinreb · Tetrahedron Letters · 1981 · 1.8K citations
Karl‐Josef Haack, Shohei Hashiguchi, Akio Fujii et al. · Angewandte Chemie International Edition in English · 1997 · 1K citations