88408-99-5Relevant academic research and scientific papers
Synthetic studies toward potent cytotoxic agents amphidinolides: Synthesis of the C1-C18 moiety of amphidinolides G, H and L
Chakraborty,Suresh
, p. 9109 - 9112 (2007/10/03)
Stereoselective synthesis of the (8S, 9S, 11R, 16S)-C1-C18 segment 1 of amphidinolides G, H and L, bearing the unique trisubstituted 's-cis-1,3- diene' moiety (C(28(29))=C13-C14=C15), has been achieved for the first time following a highly efficient convergent strategy.
Total synthesis of archaeal 36-membered macrocyclic diether lipid
Eguchi, Tadashi,Arakawa, Kenji,Terachi, Takumi,Kakinuma, Katsumi
, p. 1924 - 1933 (2007/10/03)
Total synthesis of archaeal 36-membered macrocyclic diether lipid 2 is reported. The synthesis is based upon stereoselective preparation of functionalized isoprenoid chains, ether-linkage formation between the isoprenoid chains with a glycerol derivative,
Convergent synthesis of a key intermediate for hypocholesterolemic agent 1233A, starting from methyl 3-hydroxy-2-methylpropanoate and asymmetrized bis(hydroxymethyl)acetaldehyde (BHYMA*)
Guanti, Giuseppe,Banfi, Luca,Schmid, Giovanna
, p. 4239 - 4242 (2007/10/02)
Compound 2, which is a known intermediate for the total synthesis of hypocholesterolemic agent 1233A 1, has been synthesized in good overall yield through a convergent approach, employing 3-hydroxy-2-methylpropanoate 6 and BHYMA* 5 as chiral building bloc
The First Synthesis of an Archaebacterial 36-Membered Macrocyclic Diether Lipid
Eguchi, Tadashi,Terachi, Takumi,Kakinuma, Katsumi
, p. 137 - 138 (2007/10/02)
The archaebacterial macrocyclic diether lipid featuring of 36-membered ring is synthesized by the McMurry coupling as a key step.
