✦ LIBER ✦

First syntheses of the biologically active fungal metabolites pestalotiopsones A, B, C and F

✍ Scribed by Beekman, Andrew Michael; Castillo Martinez, Edwin; Barrow, Russell Allan

Book ID: 118747398
Publisher: Royal Society of Chemistry
Year: 2013
Tongue: English
Weight: 250 KB
Volume: 11
Category: Article
ISSN: 1477-0520
DOI: 10.1039/C2OB26904J

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Total syntheses of the fungal metabolite

Total syntheses of the fungal metabolites (±)-acremines A, B and I

✍ Goverdhan Mehta; Y.C. Sunil Kumar; Tabrez Babu Khan 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 318 KB

The cytochalasins, a new class of biolog

The cytochalasins, a new class of biologically active mould metabolites

✍ Aldridge, D. C.; Armstrong, J. J.; Speake, R. N.; Turner, W. B. 📂 Article 📅 1967 🏛 Royal Society of Chemistry ⚖ 152 KB

The First Syntheses of (±)-SDEF 678 Meta

The First Syntheses of (±)-SDEF 678 Metabolite and (±)-Speciosins A–C

✍ Daniel R. Hookins; Alan R. Burns; Richard J. K. Taylor 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 498 KB

## Abstract The epoxyquinone natural products SDEF 678 metabolite, speciosin A, speciosin B and speciosin C have been prepared for the first time via a short synthetic route based around the palladium‐catalysed coupling of a halogen‐substituted 1,4‐benzoquinone monoketal, a Diels–Alder/retro‐Diels–

Two enantioselective syntheses of a prec

Two enantioselective syntheses of a precursor of the biologically most active isomer of CGA 80000 (clozylacon)

✍ H.P. Buser; B. Pugin; F. Spindler; M. Sutter 📂 Article 📅 1991 🏛 Elsevier Science 🌐 French ⚖ 593 KB

The unchlonnated precursor 4 of CGA 80000 (lJ was synthestzed enanhoselecttvely by two conceptionally dtffetent routes a) by a "choral pool" approach stamng from L-mahc acid and b) by enanttoselecttve hydrogenahon of an enamlde mtemediate. catalyzed by chual Rh-or Ru-phosphme-complexes CGA SO000 Q)

Enantioselective total syntheses of (+)-

Enantioselective total syntheses of (+)- and (−)-ottelione A and (+)- and (−)-ottelione B. Absolute configuration of the novel, biologically active natural products

✍ Goverdhan Mehta; Kabirul Islam 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 208 KB

Following our recent total synthesis of the biologically potent natural products otteliones A and B in racemic form, we have now accomplished the total synthesis of both the enantiomers of otteliones A and B through an enantiodivergent strategy emanating from the readily available Diels-Alder adduct

Enantioselective Total Syntheses of (+)-

Enantioselective Total Syntheses of (+)- and (-)-Ottelione A and (+)- and (-)-Ottelione B. Absolute Configuration of the Novel, Biologically Active Natural Products.

✍ Goverdhan Mehta; Kabirul Islam 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 63 KB 👁 2 views