guanacastepene A

An efficient intramolecular Diels-Alder (IMDA) strategy for the construction of the [5-7-6] tricyclic core (18) of… Expand

[reaction: see text] The stereoselectivity of the key epoxidation step in the synthesis of guanacastepene A is shown to be… Expand

[reaction: see text] The goal of the total synthesis of guanacastepene A served as a focus to bring together several chemical… Expand

The hydroazulene core of guanacastepene A has been synthesized in five steps from commercially available starting materials using… Expand

[reaction: see text] An approach to the highly functionalized tricyclic core of guanacastepene A has been developed using a… Expand

Studies aimed towards the total synthesis of the diterpene antibiotic, guanacastepene A, of current interest and displaying… Expand

[reaction: see text] A synthesis of the tricyclic [5-7-6] skeleton of guanacastepene A is described. The six-membered ring of… Expand

[reaction: see text] As a part of studies aimed toward the total synthesis of biologically important natural product… Expand

Studies directed towards the total synthesis of the diterpene antibiotic, guanacastepene A, of current interest and displaying… Expand

Commercially available tribromoethylene has been converted to ketoepoxide 15, an advanced intermediate in the total synthesis of… Expand