✦ LIBER ✦

Improved synthesis of 24-epibrassinolide from ergosterol

✍ Scribed by McMorris, Trevor C.; Patil, Prakash A.

Book ID: 121440999
Publisher: American Chemical Society
Year: 1993
Tongue: English
Weight: 262 KB
Volume: 58
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo00060a063

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of tritium labelled 24-epibras

Synthesis of tritium labelled 24-epibrassinolide

✍ A. Kolbe; V. Marquardt; G. Adam 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 French ⚖ 252 KB

## Abstract Deuterium and tritium 5,7,7‐tris‐labelled 24‐epibrassinolide were prepared by base catalyzed exchange reaction using 24‐epicastasterone tetraacetate 1 or bis‐isopropylidenedioxy‐24‐epicastasterone 8 and labelled water. Baeyer‐Villiger oxidation of the obtained labelled 6‐ketones 2 and 3

Synthesis of fatty acyl derivatives of 2

Synthesis of fatty acyl derivatives of 24-epibrassinolide

✍ Khripach, Vladimir A.; Zhabinskii, Vladimir N.; Tsavlovskii, Dmitrii V. 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 434 KB

New synthetic strategy for the synthesis

New synthetic strategy for the synthesis of 24-epibrassinolide

✍ Carme Brosa; Rita Puig; Xavier Comas; Cristina Fernández 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 364 KB

Synthesis of 24-epiteasterone, 24-epityp

Synthesis of 24-epiteasterone, 24-epityphasterol and their B-homo-6a-oxalactones from ergosterol

✍ Brunhilde Voigt; Jürgen Schmidt; Günter Adam 📂 Article 📅 1996 🏛 Elsevier Science 🌐 French ⚖ 502 KB

Synthesis of (22R,23R)- and (22S,23S)-[4

Synthesis of (22R,23R)- and (22S,23S)-[4-14C]-24-EPIBRASSINOLIDE

✍ S. Seo; T. Nagasaki; Y. Katsuyama; F. Matsubara; T. Sakata; M. Yoshioka; Y. Maki 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 French ⚖ 545 KB

ChemInform Abstract: Synthesis of 24-Epi

ChemInform Abstract: Synthesis of 24-Epiteasterone, 24-Epityphasterol and Their B-Homo-6a- Oxalactones from Ergosterol.

✍ B. VOIGT; J. SCHMIDT; G. ADAM 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB