Hyeung-geun Park and co-workers at Seoul National University have reported in Organic Letters on the synthesis of isonitramine.
Archive for the ‘Dieckmann condensation’ Category
An intramolecular Claisen reaction of a 1,6-diester to yield beta-ketoesters.
Isonitramine synthesis
Posted by naturalproductman on January 17, 2012
Posted in Alkaloids, Asymmetric, Dieckmann condensation, Methodology, Named Reactions, Total Synthesis | Leave a Comment »
Stemonamide Synthesis
Posted by naturalproductman on December 7, 2010
Fu-Min Zhang and co-workers at Lanzhou University have published in Chem Comm on a synthesis of stemonamide where a Schmidt reaction was used to access the 5,7-A,B-ring system.
Posted in Aldol, Alkaloids, Dieckmann condensation, Methodology, Named Reactions, Schmidt, Spirocyclic centers, Titanium, Transition Metal | Leave a Comment »
Synthesis of Streptolydigin
Posted by naturalproductman on September 29, 2010
Sergey Kozmin and co-worker from the University of Chicago have published in JACS on the total synthesis of streptolydigin.
Posted in Antibiotics, Cascade Reactions, Dieckmann condensation, Horner-Wadsworth-Emmons olefination, Methodology, Named Reactions, Polyenes, Spirocycles, Spiroketals | Leave a Comment »
Lactonamycin Synthesis
Posted by naturalproductman on September 20, 2010
Kuniaki Tatsuta and co-workers from Waseda University have published in Tetrahedron Letters on the total synthesis of lactonamycin.
Posted in Antibiotics, Cancer, Cascade Reactions, Dieckmann condensation, Methodology, Michael, Named Reactions, Polyketides | Leave a Comment »
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