1361226-71-2

Upstream product

• 1361226-68-7 tert-butyl (2S,3aS,4S,5R,6R)-4,5-bis(benzyloxy)-6-[(benzyloxy)methyl]hexahydropyrrolo[1,2-b]isoxazole-2-carboxylate 
• 64-19-7 acetic acid 
• 213617-02-8 (2R,3R,4S)-3,4-bis(benzyloxy)-2-[(benzyloxy)methyl]-3,4-dihydro-2H-pyrrole 1-oxide 

Relevant academic research and scientific papers

Total synthesis of (+)-hyacinthacine A1, (+)-7a-epi- hyacinthacine A1, (6R)-6-hydroxyhyacinthacine A1 and (6S)-6-hydroxy-7a-epi-hyacinthacine A1

The total synthesis of natural (+)-hyacinthacine A1 (6), (+)-7a-epi-hyacinthacine A1 (7) and their 6-hydroxy analogues 21 and 16 was achieved using a nitrone cycloaddition strategy with D-ribose-derived cyclic nitrone 8 as the dipole