✦ LIBER ✦

ChemInform Abstract: Synthetic Microbial Chemistry. Part 36. Synthesis and Absolute Configuration of (-)-Neuchromenin (I), a Neurotrophic Metabolite of Eupenicillium javanicum var. meloforme, and Its Enantiomer.

✍ Scribed by Yoshihisa Tanada; Kenji Mori

Publisher: John Wiley and Sons
Year: 2010
Weight: 27 KB
Volume: 33
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200209236

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and Absolute Configuration of

Synthesis and Absolute Configuration of (−)-Neuchromenin, a Neurotrophic Metabolite of Eupenicillium javanicum var. meloforme, and Its Enantiomer

✍ Yoshihisa Tanada; Kenji Mori 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 270 KB

Both the enantiomers of neuchromenin 1 (2,3-dihydro-8,9-dihydroxy-2-methyl-4H,5H-pyrano[3,2-c][1]benzopyran-4-one) were synthesized starting from the enantiomers of ethyl 3- [ ‡] Synthetic Microbial Chemistry, XXXVI.

ChemInform Abstract: Synthetic Microbial

ChemInform Abstract: Synthetic Microbial Chemistry. Part 32. Synthesis and Absolute Configuration of Hongoquercin A, an Antibacterial Sesquiterpene-Substituted Orsellinic Acid Isolated as a Fungal Metabolite.

✍ Hisayuki Tsujimori; Masahiko Bando; Kenji Mori 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB

ChemInform Abstract: Synthetic Microbial

ChemInform Abstract: Synthetic Microbial Chemistry. Part 37. Synthesis and Absolute Configuration of Nocardione A and B, Furano-o-naphthoquinone-Type Metabolites of Nocardia sp. with Antifungal, Cytotoxic, and Enzyme Inhibitory Activities.

✍ Yoshihisa Tanada; Kenji Mori 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 views