340254-93-5

Upstream product

• 340254-88-8 1-hydro-5-carbaphosphatrane 
• 74-88-4 methyl iodide 
• 423774-54-3 5,5',5''-tri-tert-butyl-2,2',2''-trimethoxytriphenylmethanol 
• 340254-90-2 5,5',5''-tri-tert-butyl-2,2',2''-trimethoxytriphenylmethane 
• 340254-96-8 4-tert-butyl-2-(3,6-di-tert-butyl-9a-thioxo-9,10-dioxa-9aλ⁵-phospha-indeno[1,2-a]inden-4b-yl)-phenol 
• 340254-92-4 5-tert-butyl-3,3-bis-(5-tert-butyl-2-methoxy-phenyl)-3H-benzo[d][1,2]oxaphosphole 2-oxide 
• 41280-65-3 2-bromo-4-tert-butylanisole 

Relevant academic research and scientific papers

Reactivity of 1-hydro-5-carbaphosphatrane based on tautomerization between pentavalent phosphorane and trivalent cyclic phosphonite

The reaction behavior of 1-hydro-5-carbaphosphatrane (1a) was examined. Treatment of 1a with oxidants such as 3-chloroperoxybenzoic acid (mCPBA) and tBuOCl gave cyclic phosphonate 2 and 1-chloro-5-carbaphosphatrane (4), respectively, via cyclic phosphonit

Synthesis, structure, and bonding properties of 5-carbaphosphatranes: A new class of main group atrane

1-Hydro-5-carbaphosphatrane (1) and 1-methyl-5-carbaphosphatrane (2), the first 5-carbon analogues of phosphatranes, were synthesized by a demethylation reaction of cyclic phosphinate 3. X-ray analysis revealed that 1 has a typical trigonal bipyramidal st