126655-21-8Relevant articles and documents
Stereocomplementary routes to hydroxylated nitrogen heterocycles: Total syntheses of casuarine, Australine, and 7-epi-Australine
Parmeggiani, Camilla,Cardona, Francesca,Giusti, Leonardo,Reissig, Hans-Ulrich,Goti, Andrea
, p. 10595 - 10604 (2013)
Addition of lithiated 1-benzyloxyallene to a D-arabinose-derived cyclic nitrone occurred with perfect diastereoselectivity furnishing a bicyclic 1,2-oxazine derivative, which is an excellent precursor for pyrrolizidine alkaloids hydroxylated at C-7 with o
Asymmetric synthesis of ( - )-7-epiaustraline and (+)-1,7-diepiaustraline
Tang, Minyan,Pyne, Stephen G.
, p. 7818 - 7824 (2007/10/03)
A diastereoselective and modular approach to the synthesis of the 3-hydroxymethyl-2,3,5,6,7,7a-hexahydro-1H-pyrrolizine-1,2,7-triol structure, characteristic of several natural pyrrolizidine natural products, has been developed. This approach culminated i
Synthesis of (1R,2R,3R,7R,7aR)-hexahydro. 3-(hydroxymethyl)- 1H- pyrrolizine-1,2,7-triol: 7-Epiaustraline [6]
Denmark,Herbert
, p. 7357 - 7358 (2007/10/03)
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