Total Synthesis of Gymnoconjugatins A and B
- 29 November 2006
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 71 (26) , 9841-9844
- https://doi.org/10.1021/jo061755c
Abstract
Convergent and efficient syntheses of the microbial natural products gymnoconjugatin A and B are reported and were based on a linchpin coupling strategy using a boron/tin hetero-bis-metallated butadiene system.Keywords
This publication has 24 references indexed in Scilit:
- Roquefortine E, a Diketopiperazine from an Australian Isolate of Gymnoascus reessiiJournal of Natural Products, 2005
- Total Synthesis of Lucilactaene, A Cell Cycle Inhibitor Active in p53-Inactive CellsJournal of the American Chemical Society, 2005
- Gymnoascolides A−C: Aromatic Butenolides from an Australian Isolate of the Soil Ascomycete Gymnoascus reessiiJournal of Natural Products, 2005
- Three pyrrolyloctatetraenyl-α-pyrones from Auxarthron conjugatumPhytochemistry, 1999
- Total Synthesis of (−)-Solanapyrone A via Enzymatic Diels−Alder Reaction of ProsolanapyroneThe Journal of Organic Chemistry, 1998
- Palladium-Catalyzed Cross-Coupling Reactions of Organoboron CompoundsChemical Reviews, 1995
- Convergent syntheses of luteoreticulin and didemethylluteoreticulinJournal of Heterocyclic Chemistry, 1995
- 5-(3-carboxymethoxyphenyl)-2-(4,5-dimethylthiazolyl)-3-(4-sulfophenyl)tetrazolium, inner salt (MTS) and related analogs of 3-(4,5-dimethylthiazolyl)-2,5-diphenyltetrazolium bromide (MTT) reducing to purple water-soluble formazans As cell-viability indicatorsBioorganic & Medicinal Chemistry Letters, 1991
- The Palladium‐Catalyzed Cross‐Coupling Reactions of Organotin Reagents with Organic Electrophiles [New Synthetic Methods (58)]Angewandte Chemie International Edition in English, 1986
- A Facile Synthesis of 6-Conjugated 2-PyronesSynthesis, 1975