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Total synthesis of (±)-pterocarpin and (±)-pisatin

✍ Scribed by Kenji Fukui; Mitsuru Nakayama

Book ID
104250253
Publisher
Elsevier Science
Year
1966
Tongue
French
Weight
149 KB
Volume
7
Category
Article
ISSN
0040-4039

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📜 SIMILAR VOLUMES

ChemInform Abstract: Asymmetric Total Sy
ChemInform Abstract: Asymmetric Total Synthesis of (+)-Pisatin, a Phytoalexin from Garden Peas (Pisum sativum L.).
✍ E. PINARD; M. GAUDRY; F. HENOT; A. THELLEND 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB

Asymmetric Total Synthesis of (+)-Pisatin, a Phytoalexin from Garden Peas (Pisum sativum L.). -Based on a modified Sharpless asymmetric dihydroxylation of the 2H-1-benzopyran (II) and following hydrogenenative cyclization, a short asymmetric total synthesis of (+)-pisatin (VI) is realized. -(

Syntheses of pterocarans, I. Synthesis o
Syntheses of pterocarans, I. Synthesis of both the enantiomers of pterocarpin
✍ Mori, Kenji ;Kisida, Hirosi 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 357 KB

Thc first synthesis of (-)-pterocarpin (6) was achieved by rcsolving (\*)-2, which in turn was prepared from a known isonavone (1). Unnatural (+ tpterocarpin was also synthesized. (-)-Pterocarpin (6) was first isolated by Cazeneuve in 1874 as a constituent of red sandalwood, Pterocarpus suntalinus