158348-12-0

Upstream product

• 96-22-0 pentan-3-one 
• 89-67-8 α-D-glucoheptonic γ-lactone 

Downstream Products

• 158348-25-5 {(3aR,4R,5aS,8R,9aS,9bS)-4-[(E)-(S)-5-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxy)-4-oxo-pent-2-enyl]-2,2-diethyl-octahydro-[1,3]dioxolo[4,5-d]pyrano[3,2-b]pyran-8-yl}-acetic acid methyl ester 
• 870700-32-6 [6-(6-{5-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-4-methylene-tetrahydro-furan-2-yl}-4-oxo-1-triethylsilanyloxy-hex-2-enyl)-7,8-bis-triethylsilanyloxy-octahydro-pyrano[3,2-b]pyran-2-yl]-acetic acid methyl ester 
• 934715-99-8 N-benzyl-5-O-tert-butyldimethylsilyl-1,4-dideoxy-2,3:6,7-di-O-diethyliden-1,4-imino-D-glycero-L-talo-heptitol 
• 934716-01-5 N-benzyl-5-O-tert-butyldimethylsilyl-1,4-dideoxy-2,3-O-diethyliden-1,4-imino-D-glycero-L-talo-heptitol 
• 934716-02-6 N-benzyl-1,4-imino-D-glycero-L-talo-heptitol 
• 934716-03-7 N-benzyl-1,4-dideoxy-1,4-imino-L-mannitol 

Relevant academic research and scientific papers

Halichondrin B: Synthesis of the C(1)-C(15) subunit

A short and efficient synthesis of the C(1)-C(15) subunit of halichondrin B in its natural configuration is described. The polycyclic caged ketal 3, containing nine asymmetric centers, is prepared in 14 steps from α-D-glucoheptonic acid γ-lactone (7). Key steps in the two similar routes described include EtMgBr-promoted pinacol ring expansions of hydrory mesylates 23 and 34. intramolecular Michael additions of 29 and 37, and a one-pot, HF-induced conversion of 4 to 3 involving in situ silyl ether cleavage, acetal hydrolysis, Michael addition, and caged ketal formation. Alternative protocols for carbinol inversion at C(11), one early and one late in the synthetic sequence, are also described.