✦ LIBER ✦

Stereoselective total synthesis of racemic (3S,4R/3R,4S)- and a diastereoisomeric mixture of (6E, 10Z)-3,4,7,11-tetramethyl-trideca-6,10-dienal (faranal); the trail pheromone of the Pharaoh's ant

✍ Scribed by Baker, Raymond; Billington, David C.; Ekanayake, Neelakanthie

Book ID: 121524205
Publisher: Royal Society of Chemistry
Year: 1983
Weight: 989 KB
Category: Article
ISSN: 1472-7781
DOI: 10.1039/P19830001387

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Pheromone synthesis, CLXX. A new synthes

Pheromone synthesis, CLXX. A new synthesis of faranal [(3S,4R,6E,10Z)-3,4,7,11-tetramethyl-6,10-tridecadienal], the trail pheromone of the pharaoh's ant,Monomorium pharaonis

✍ Mori, Kenji ;Murata, Noriaki 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 352 KB 👁 1 views

## Abstract Faranal (1), the trail‐following pheromone of the worker of Pharaoh's ant (__Monomorium pharaonis__), was synthesized by the coupling reaction of the iododiene 3 with the chiral building block 8 as the key step. The geometrically pure iododiene 3 was prepared by the zirconocene‐mediated

ChemInform Abstract: Pheromone Synthesis

ChemInform Abstract: Pheromone Synthesis. Part 170. A New Synthesis of Faranal ((3S,4R,6E, 10Z)-3,4,7,11-Tetramethyl-6,10-tridecadienal), the Trail Pheromone of the Pharaoh′s Ant, Monomorium pharaonis.

✍ K. MORI; N. MURATA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB

Synthesis of (3S*,4R*,6E,10Z )-3,4,7,11-

Synthesis of (3S*,4R*,6E,10Z )-3,4,7,11-tetramethyltrideca-6,10-dienal (faranal) using stereospecific 1,4-cis-hydrogenation of conjugated double bonds

✍ Vasil’ev, Andrei A.; Engman, Lars; Serebryakov, Edward P. 📂 Article 📅 2000 🏛 Royal Society of Chemistry ⚖ 143 KB

ChemInform Abstract: Synthesis of (3S*,4

ChemInform Abstract: Synthesis of (3S*,4R*,6E,10Z)-3,4,7,11-Tetramethyltrideca-6,10-dienal (Faranal) Using Stereospecific 1,4-cis-Hydrogenation of Conjugated Double Bonds.

✍ Andrei A. Vasil'ev; Lars Engman; Edward P. Serebryakov 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 39 KB 👁 1 views

Total synthesis of natural products havi

Total synthesis of natural products having 1,3-syn-polyol, δ-lactone of (2Z,5S,7S,9R,11R)-tetrahydroxyhexacos-2-enoic acid and 4,6,8,10,12,14,16,18,20-all-syn-nonamethoxy-1-pentacosene

✍ Tadashi Nakata; Toshiro Suenaga; Koichi Nakashima; Takeshi Oishi 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 261 KB

Synthesis and Structure of [Sn4Se11]6–,

Synthesis and Structure of [Sn4Se11]6–, 3.0.CO;2-M/asset/equation/tex2gif-stack-1.gif?v=1&t=h5l55r5t&s=b439cdb160594bc76a5be3d9bf20c7c44cb6e3bd" class="inlineGraphic"> [Sn2Se52–], and 3.0.CO;2-M/asset/equation/tex2gif-stack-2.gif?v=1&t=h5l55r5t&s=155c1d4a988fd3c89485d09b17a5955efa65189b" class="inlineGraphic"> [Sn3Se72–] – Model Anions for the Solventothermal Reaction Pathway to Lamellar Selenidostannates(IV)

✍ Anja Loose; William S. Sheldrick 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 German ⚖ 205 KB 👁 2 views

Reaction of A 2 CO 3 (A = K, Rb) with Sn and Se in an H 2 O/CH 3 OH mixture at 115±130 °C affords the isotypic selenidostannates(IV) A 6 Sn 4 Se 11 ´x H 2 O (A = K, x = 8) 1 and 2 whose discrete [Sn 4 Se 11 ] 6± anions each contain two corner-bridged ditetrahedral [Sn 2 Se 6 ] 4± species. Similar re