𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A chiron approach to (1R,2R,5S,7S)-2-hydroxy-exo-brevicomin: a component of the volatiles produced by the male mountain pine beetle, Dendroctonus ponderosae

✍ Scribed by D. Naveen Kumar; B. Venkateswara Rao; G.S. Ramanjaneyulu

Book ID
108283935
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
120 KB
Volume
16
Category
Article
ISSN
0957-4166

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Pheromone Synthesis, CLXXXIII. Synthesis
Pheromone Synthesis, CLXXXIII. Synthesis of (1R,2R,5S,7R)- and (1R,2S,5S,7R)-2-hydroxy-exo-Brevicomin, the Components of the Male-Produced Volatiles of the Mountain Pine Beetle,dendroctonus ponderosae
✍ Takikawa, Hirosato ;Shimbo, Ken-Ichiro ;Mori, Kenji 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 441 KB

## Abstract Both (2__R__)‐ and (2__S__)‐hydroxy derivatives of (+)‐exo‐brevicomin {5‐methyl‐6,8‐dioxabicyclo[3.2.1]octan‐2‐ol; 1 and 2} were synthesized by employing Sharpless asymmetric dihydroxylation as the key reaction.

ChemInform Abstract: Pheromone Synthesis
ChemInform Abstract: Pheromone Synthesis. Part 183. Synthesis of (1R,2R,5S,7R)- and (1R,2S, 5S,7R)-2-Hydroxy-exo-brevicomin, the Components of the Male-Produced Volatiles of the Mountain Pine Beetle, Dendroctonus ponderosae.
✍ H. TAKIKAWA; K. SHIMBO; K. MORI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

Pheromone Synthesis. Part 183. Synthesis of (1R,2R,5S,7R)-and (1R,2S, 5S,7R)-2-Hydroxy-exo-brevicomin, the Components of the Male-Produced Volatiles of the Mountain Pine Beetle, Dendroctonus ponderosae. -Both title compounds (V) and (VI) are synthesized via asymmetric dihydroxylation as the key ste

Pheromone Synthesis, CLXXXII. Synthesis
Pheromone Synthesis, CLXXXII. Synthesis of (1R,1′R,5′R,7′R)- and (1S,1′R,5′R,7′R)- 1-hydroxy-exo-Brevicomin, the Components of the Male-Produced Volatiles of the Mountain Pine Beetle,dendroctonus ponderosae
✍ Yokoyama, Yūsuke ;Mori, Kenji 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 491 KB

## Abstract Both (1__R__)‐ and (1__S__)‐hydroxy derivatives of (+)‐exo‐brevicomin {(1__R__,1′__R__,5′__R__,7′__R__)‐1‐(5′‐methyl‐6′,8′‐dioxabicyclo[3.2.1]‐octyl)ethanol (1) and its (1__S__)‐isomer (2)} were synthesized by employing Sharpless asymmetric dihydroxylation as the key reaction.