Enantioselective total synthesis of macrosphelides A and E

No abstract is available for this paper.

• Publication year

  2011

• Venue

  Tetrahedron

• Publication date

  2011-06-24

• Fields of study

  Chemistry

• Identifiers
  DOI 10.1016/J.TET.2011.04.099
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

• Concise syntheses of (+)-macrosphelides A and B: studies on the macro-ring closure strategy.

  2009cited by this paper
• Mitsunobu and related reactions: advances and applications.

  2009cited by this paper
• Design, synthesis, and biological evaluation of artificial macrosphelides in the search for new apoptosis-inducing agents.

  2009cited by this paper
• Cell-adhesion Inhibitors Produced by a Sea Hare-derived Periconia sp.

  2007cited by this paper
• Synthesis of macrosphelides with a thiazole side chain: new antitumor candidates having apoptosis-inducing property.

  2006cited by this paper
• Concise syntheses of (+)-macrosphelides A and B.

  2005cited by this paper
• Total synthesis of macrosphelides A, B, and E: first application of ring-closing metathesis for macrosphelide synthesis.

  2004cited by this paper
• A combinatorial synthesis of a macrosphelide library utilizing a palladium-catalyzed carbonylation on a polymer support.

  2003cited by this paper
• New strategy for the total synthesis of macrosphelides a and B based on ring-closing metathesis.

  2003cited by this paper
• Total synthesis of macrosphelide A by way of palladium-catalyzed carbonylative esterification

  2003cited by this paper
• Absolute stereostructures of cell adhesion inhibitors, macrosphelides H and L, from Periconia byssoides OUPS-N133.

  2002cited by this paper
• The total synthesis of macrosphelides A and E from carbohydrate precursors

  2002cited by this paper
• Furan ring oxidation strategy for the synthesis of macrosphelides A and B.

  2001cited by this paper
• Absolute stereostructures of cell-adhesion inhibitors, macrosphelides C, E–G and I, produced by a Periconia species separated from an Aplysia sea hare

  2001cited by this paper
• Total syntheses of macrosphelides (+)-A, (−)-A and (+)-E

  2000cited by this paper
• Total synthesis of macrosphelides B and A

  2000cited by this paper
• New members of the macrosphelides from Microsphaeropsis sp. FO-5050 IV.

  1999cited by this paper
• Novel antitumour metabolites produced by a fungal strain from a sea hare

  1997cited by this paper
• Relative and Absolute Stereochemistries and Total Synthesis of (+)-Macrosphelides A and B, Potent, Orally Bioavailable Inhibitors of Cell−Cell Adhesion

  1997cited by this paper
• Macrosphelides C and D, novel inhibitors of cell adhesion.

  1997cited by this paper
• Macrosphelide, a novel inhibitor of cell-cell adhesion molecule. II. Physiochemical properties and structural elucidation.

  1996cited by this paper
• Macrosphelide, a novel inhibitor of cell-cell adhesion molecule. I. Taxonomy, fermentation, isolation and biological activities.

  1995cited by this paper
• Convenient method for the preparation of trityl ethers from secondary alcohols

  1992cited by this paper
• Structure-activity relationships in the 2-arylcarbapenem series: synthesis of 1-methyl-2-arylcarbapenems.

  1987cited by this paper
• The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products

  1981cited by this paper

• The Potential of Arctic Pseudogymnoascus Fungi in the Biosynthesis of Natural Products

  2023cites this paper
• Total synthesis of (+)-γ-lycorane from ethyl lactate using iterative Claisen and Overman rearrangement reactions

  2020cites this paper
• Anti-addition of Dimethylsulfoxonium Methylide to Acyclic α,β-Unsaturated Ketones and Its Application in Formal Synthesis of an Eicosanoid

  2017cites this paper
• Enantiospecific formal total synthesis of iriomoteolide 3a.

  2014cites this paper
• Total synthesis of (+)-seimatopolide A.

  2014cites this paper
• Synthetic Advances in Macrosphelides: Natural Anticancer Agents

  2014cites this paper
• Development of an Advanced Synthetic Route to Macrosphelides and Its Application to the Discovery of a More Potent Macrosphelide Derivative

  2014cites this paper
• Enantioselective synthesis of macrolactone core of the natural product Sch725674

  2014cites this paper
• Design and synthesis of a macrosphelide A-biotin chimera.

  2014cites this paper
• Update 1 of: macrolactonizations in the total synthesis of natural products.

  2013cites this paper
• Enantiospecific total synthesis of indole alkaloids (+)-eburnamonine, (−)-aspidospermidine and (−)-quebrachamine

  2013cites this paper
• Total synthesis and determination of the absolute configuration of 5,6-dihydro-α-pyrone natural product synargentolide B.

  2013cites this paper
• Total synthesis of varitriol, varioxirane, and enantiomer of the proposed biosynthetic precursor.

  2013cites this paper
• Total Synthesis of Macrosphelide M from Diacetone Glucose

  2012cites this paper
• Electronic helix theory-guided rational design of kinetic resolutions by means of the Sharpless asymmetric dihydroxylation reactions

  2012cites this paper
• Dihydroazamacrosphelides: Synthesis and Apoptosis Inducing Activities.

  2011cites this paper
• Binary fluorous tagging enables the synthesis and separation of a sixteen-stereoisomer library of macrosphelides

  2011cites this paper