71939-43-0Relevant 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.
Total synthesis of (+)-obtusenyne
Fujiwara, Kenshu,Awakura, Daisuke,Tsunashima, Misa,Nakamura, Akira,Honma, Teruki,Murai, Akio
, p. 2616 - 2617 (2007/10/03)
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