✦ LIBER ✦

An improved route to a key hydroazulenone intermediate for helenanolide synthesis

✍ Scribed by Grieco, Paul A.; Ohfune, Yasufumi

Book ID: 121326159
Publisher: American Chemical Society
Year: 1980
Tongue: English
Weight: 560 KB
Volume: 45
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo01299a043

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

An improved route to an intermediate in

An improved route to an intermediate in podophyllotoxin synthesis

✍ Murphy, William S.; Wattanasin, Sompong 📂 Article 📅 1980 🏛 The Royal Society of Chemistry 🌐 English ⚖ 174 KB

Stereocontrolled route to a key intermed

Stereocontrolled route to a key intermediate for the synthesis of maytansine

✍ E.J. Corey; Mark G. Bock 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 210 KB

We have undertaken a synthesis of this substance as part of a broader program in the area of biologically active macrocyclic natural products. One attractive approach to the synthesis of maytansine involves the introduction of chiraltty at carbons 3, 4, 5, 10, and 9 after formation of the macro ring

Short and Versatile Route to a Key Inter

Short and Versatile Route to a Key Intermediate for Lactacystin Synthesis.

✍ Philip C. Bulman Page; A. Sazali Hamzah; David C. Leach; Steven M. Allin; David 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 23 KB 👁 1 views

Short and Versatile Route to a Key Inter

Short and Versatile Route to a Key Intermediate for Lactacystin Synthesis

✍ Bulman Page, Philip C.; Hamzah, A. Sazali; Leach, David C.; Allin, Steven M.; An 📂 Article 📅 2003 🏛 American Chemical Society 🌐 English ⚖ 53 KB

An improved procedure for the Blaise rea

An improved procedure for the Blaise reaction: a short, practical route to the key intermediates of the saxitoxin synthesis

✍ Hannick, Steven M.; Kishi, Yoshito 📂 Article 📅 1983 🏛 American Chemical Society 🌐 English ⚖ 465 KB

A simple route to a key intermediate for

A simple route to a key intermediate for the synthesis of 11-desoxyprostaglandins

✍ E.J. Corey; T. Ravindranathan 📂 Article 📅 1971 🏛 Elsevier Science 🌐 French ⚖ 148 KB

received in U.K. for publication 8 Iiovember 1971) 11-Desoxyproetaglandlna are of considerable current interest as possible substrates for mlcrobiological hydroxylatlon at C(ll) (pro&mold numbering) and elsewhere, as poaslble antagonlsta of the prostagl&dlns in the E and F series, and as hypotenslve