876064-57-2Relevant articles and documents
Synthesis of (+)-obtusenyne
Mak, S.Y. Frankie,Curtis, Neil R.,Payne, Andrew N.,Congreve, Miles S.,Wildsmith, Andrew J.,Francis, Craig L.,Davies, John E.,Pascu, Sofia I.,Burton, Jonathan W.,Holmes, Andrew B.
experimental part, p. 2867 - 2885 (2009/06/17)
An enantioselective synthesis of the halogenated medium-ring ether natural product (+)-obtusenyne is reported which uses the ring expansion of a seven-membered ketene acetal by means of a Claisen rearrangement to construct the core nine-membered oxygen he
A synthesis of (+)-obtusenyne
Frankie Mak,Curtis, Neil R.,Payne, Andrew N.,Congreve, Miles S.,Francis, Craig L.,Burton, Jonathan W.,Holmes, Andrew B.
, p. 3199 - 3201 (2007/10/03)
A synthesis of the halogenated medium-ring ether natural product (+)-obtusenyne is reported utilizing a Claisen rearrangement and an intramolecular hydrosilation as key steps. Georg Thieme Verlag Stuttgart.
