A stereocontrolled synthesis of (2,3,5,13,14)- (+)-Aplidiasphingosine, a marine terpenoid
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Aplidiasphingosine, an antimicrobial and antitumor terpenoid from an Aplidium species (marine tunicate)
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3. Stereochemistry of aplidiasphingosine as proposed by the asymmetric synthesis and 13c-nmr study of sphingosine relatives
4. Absolute configuration of (−)-4-methylheptan-3-ol, a pheromone of the smaller european elm bark beetle, as determined by the synthesis of its (3R,4R)-(+)- and (3S,4R)-(+)-isomers
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2. Ascidians (Tunicates)-2;Encyclopedia of Marine Natural Products;2014-08-07
3. Optically pure γ-butyrolactones and epoxy esters via two stereocentered HKR of 3-substituted epoxy esters: a formal synthesis of (−)-paroxetine, Ro 67-8867 and (+)-eldanolide;Organic & Biomolecular Chemistry;2013
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5. The Synthesis of Insect Pheromones, 1979-1989;Total Synthesis of Natural Products;2007-02-20
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