67217-83-8Relevant articles and documents
Intramolecular nitrone dipolar cycloadditions: Control of regioselectivity and synthesis of naturally-occurring spirocyclic alkaloids
Hodges, Alastair J.,Bond, Andrew D.,Holmes, Andrew B.,Roughley, Stephen D.,Smith, Catherine J.,Adams, Joseph P.,Ryan, John H.,Saubern, Simon,Newton, Annabella F.,Press, Neil J.,Turnbull, Michael D.
, p. 8963 - 8974,12 (2012/12/12)
The intramolecular nitrone dipolar cycloaddition of in situ-generated nitrones such as compound 26 has been used for the synthesis of cyclic isoxazolidines 27 and 29. The regioselectivity of the intramolecular cycloaddition depends on the nature of the terminal substituent on the dipolarophile. The influence of the substituent on the regioselectivity of the cycloaddition has been examined using several model systems and two methods of nitrone formation. These studies demonstrated that the cyano-substituent plays a special role in favouring the formation of the 6,6,5-ring fused adduct 27 under thermodynamically controlled conditions. The utility of the cyclo-adduct 57 (see Scheme 12) as a precursor for the naturally occurring histrionicotoxins is illustrated by the synthesis of three "unsymmetrical" (i.e. with each side chain bearing different functional groups) members of the histrionicotoxin family HTX-259A, HTX-285C and HTX-285E (2, 3 and 4 respectively).
The total synthesis of alkaloids (-)-histrionicotoxin 259A, 285C and 285E.
Smith, Catherine J,Holmes, Andrew B,Press, Neil J
, p. 1214 - 1215 (2007/10/03)
The first total syntheses of three "unsymmetrical" (i.e. different terminal groups in the side chains) members of the histrionicotoxin family of alkaloids have been accomplished via stepwise introduction of the two side chain moieties onto a common tricyc
