786668-40-4Relevant academic research and scientific papers
Synthesis of the ABC tricyclic fragment of the pectenotoxins via stereocontrolled cyclization of a γ-hydroxyepoxide appended to the AB spiroacetal unit
Halim, Rosliana,Brimble, Margaret A.,Merten, Joern
, p. 1387 - 1399 (2007/10/03)
The stereocontrolled synthesis of the C1-C16 ABC spiroacetal-containing tricyclic fragment of pectenotoxin-7 6 has been accomplished. The key AB spiroacetal aldehyde 9 was successfully synthesized via acid catalyzed cyclization of protected ketone precurs
Synthesis of the ABC fragment of the pectenotoxins
Halim, Rosliana,Brimble, Margaret A.,Merten, Joern
, p. 2659 - 2662 (2007/10/03)
(Chemical Equation Presented) A highly stereocontrolled synthesis of the C1-C16 ABC spiroacetal-containing fragment 5 of PTX7 (4) has been achieved. Appendage of the C ring to the AB fragment involved Wittig reaction of spiroacetal aldehyde 8 with a stabi
Access to both anomers of pectenotoxin spiroketals by kinetic spiroketalization
Pihko, Petri M.,Aho, Jatta E.
, p. 3849 - 3852 (2007/10/03)
A concise synthesis of both AB ring spiroisomers of the pectenotoxins is described. The nonanomeric AB spiroketal ring system of the pectenotoxins-1, -2, -3, and -6 is formed under very mild, kinetic spiroketalization conditions, along with the anomeric i
