910042-96-5Relevant articles and documents
Toward the development of a general chiral auxiliary. A total synthesis of (+)-tetronolide via a tandem ketene-trapping [4 + 2] cycloaddition strategy
Boeckman Jr., Robert K.,Shao, Pengcheng,Wrobleski, Stephen T.,Boehmler, Debra J.,Heintzelman, Geoffrey R.,Barbosa, Antonio J.
, p. 10572 - 10588 (2007/10/03)
A highly convergent, enantioselective total synthesis of the aglycone of the tetrocarcins, (+)-tetronolide, is described. The synthesis highlights the use of several new methods, including camphor auxiliary-directed asymmetric alkylation and the enantiose