76741-12-3Relevant academic research and scientific papers
The C2 selective nucleophilic substitution reactions of 2,3-epoxy alcohols mediated by trialkyl borates: The first endo-mode epoxide-opening reaction through an intramolecular metal chelate
Sasaki, Minoru,Tanino, Keiji,Hirai, Atsushi,Miyashita, Masaaki
, p. 1789 - 1791 (2007/10/03)
(Matrix presented) Highly efficient C2 selective substitution reactions of 2,3-epoxy alcohols with nucleophiles were developed by using NaN 3-(CH3O)3B, NaSPh-(CH3O) 3B, or NaCN-(C2H5/
Synthesis of (-)-Invictolide, the Pheromone Component of the Red Imported Fire Ant
Senda, Shuji,Mori, Kenji
, p. 1379 - 1384 (2007/10/02)
(-)-Invictolide was synthesized in 16 steps from 2-methylpentanal.
SYNTHESIS OF BOTH THE ENANTIOMERS OF INVICTOLIDE, A PHEROMONE COMPONENT OF THE RED IMPORTED FIRE ANT
Mori, Kenji,Nakazono, Yutaka
, p. 6459 - 6464 (2007/10/02)
Both the enantiomers of invictolide were synthesized in 17 steps from propargyl alcohol.
PREPARATION OF THE BOTH ENANTIOMERS OF THREO-2-AMINO-3-METHYLHEXANOIC ACID BY ENZYMATIC. RESOLUTION AND THEIR CONVERSION TO OPTICALLY ACTIVE FORMS OF THREO-4-METHYLHEPTAN-3-OL, A PHEROMONE COMPONENT OF THE SMALLER EUROPEAN ELM BARK BEETLE
Mori, Kenji,Iwasawa, Hiroko
, p. 2209 - 2213 (2007/10/02)
The both enantiomers of threo-2-amino-3-methylhexanoic acid were prepared by resolving its racemic N-acetate with Aspergillus acylase.The amino acid enantiomers were converted to optically active forms of threo-4-methylheptan-3-ol, a pheromone component of Scolytus multistriatus.
