𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Formal total synthesis of (±)-herbertenediol and (±)-mastigophorenes A and B

✍ Scribed by A Srikrishna; M.Srinivasa Rao


Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
64 KB
Volume
42
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


First synthesis of mastigophorenes A and
✍ Gerhard Bringmann; Thomas Pabst; David S. Rycroft; Joseph D. Connolly 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 206 KB

The first synthesis of mastigophorenes A and B by oxidative phenolic coupling of partially protected derivatives of their joint natural monomeric half, herbertenediol, is described. The synthesis starts from this diol itself or from the corresponding aldehyde, both available by isolation from the li

ChemInform Abstract: Total Syntheses of
✍ Andrew P. Degnan; A. I. Meyers 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

Total Syntheses of (-)-Herbertenediol (I), (-)-Mastigophorene A (II), and (-)-Mastigophorene B (III). Combined Utility of Chiral Bicyclic Lactams and Chiral Aryl Oxazolines.

Synthesis of (-)-herbertenediol and (aR,
✍ Ai-Min Zhang; Guo-Qiang Lin 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 575 KB

## Abstract Total enantioselective synthesis of the natural (‐)‐Herbertenediol (1) was accomplished in eleven steps with an overall yield of 15% starting from the 2‐methoxy‐4‐methyl‐phenol. The total synthesis features asymmetric intramolecular Heck reaction and Wolff‐Kishner‐Huang reduction. (a__R