83600-35-5Relevant academic research and scientific papers
AN IMPROVED PROCEDURE FOR THE CONVERSION OF INDOLINES INTO INDOLES
Ninomiya, Ichiya,Kiguchi, Toshiko,Hashimoto, Chiyomi,Barton, Derek H. R.,Lusinchi, Xavier,Milliet, Pierre
, p. 4183 - 4186 (2007/10/02)
The addition of a sacrificial enamine (such as indole), or of a vinyl ether (like dihydropyran) to an indoline during dehydrogenation by phenylseleninic anhydride dramatically improves the yield of the corresponding indole.This is due to scavenging of Se
Formal Total Synthesis of (+/-)-Pseudomonic Acids from Dihydropyran
Jackson, Richard F. W.,Raphael, Ralf A.,Stibbard, John H. A,Tidbury, Raymond C.
, p. 2159 - 2164 (2007/10/02)
A new, convenient, and stereoselective route to a central intermediate in pseudomonic acid synthesis via the cis-fused γ-lactone, 2,7-dioxabicyclonon-4-en-8-one (3), is described.The required relative stereochemistry of the 2- and 5-side chains is established by a palladium(0)-mediated allylic substitution of the γ-lactone (3) by di-t-butylsodiomalonate.
AN APPROACH TO THE SYNTHESIS OF PSEUDOMONIC ACIDS
Raphael, Ralph A.,Stibbard, John H A,Tidbury, Raymond
, p. 2407 - 2410 (2007/10/02)
The synthesis of the cis-fused γ-lactone 2,7-dioxa-bicyclo-(4,3,O)non-4-en-8-one (3) by two routes is reported.Its stereoselective conversion to a key intermediate for pseudomonic acid synthesis is described.
