192725-91-0

Upstream product

• 192725-90-9 tert-butyl 2-(prop-2-en-1-yl)hydrazinecarboxylate 
• 13139-17-8 N-(Benzyloxycarbonyloxy)succinimide 
• 57699-88-4 1-tert-butoxycarbonyl-2-carbobenzyloxyhydrazine 
• 106-95-6 allyl bromide 

Downstream Products

• 627908-61-6 C₂₀H₂₈N₂O₄ 
• 706808-56-2 C₁₉H₂₆N₂O₄ 
• 706808-60-8 C₁₉H₂₄N₂O₄ 
• 192725-92-1 N^β-(benzyloxycarbonyl)-N^α-(tert-butoxycarbonyl)-N^β-(formylmethyl)hydrazide 
• 706808-77-7 1,4-dihydro-phthalazine-2,3,5,6-tetracarboxylic acid 3-benzyl ester 2-tert-butyl ester 5,6-dimethyl ester 
• 706808-74-4 1,4,4a,7-tetrahydro-phthalazine-2,3,5,6-tetracarboxylic acid 3-benzyl ester 2-tert-butyl ester 5,6-dimethyl ester 
• 706808-71-1 4-vinyl-3,6-dihydro-pyridazine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester 
• 627908-62-7 4,7-dihydro-3H-[1,2]diazepine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester 
• 706808-63-1 3,6-dihydro-pyridazine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester 
• 140200-92-6 3,6-Dihydro-2H-pyridazine-1-carboxylic acid benzyl ester 

Relevant academic research and scientific papers

Synthesis of cyclic hydrazines by ring-closing metathesis of dienes and enynes tethered by an N-N bond

Ring-closing metathesis of dienes and enynes tethered by an N-N bond produced 6- to 10-membered cyclic 1,2-diaza compounds. The enyne RCM adducts were further transformed by Diels-Alder reaction into aromatic compounds.

Retroviral protease inhibiting compounds

A compound comprising a substituent of the formula (II) is disclosed as an HIV protease inhibitor. Intermediates for making such compounds and processes for making such intermediates are also disclosed.

RETROVIRAL PROTEASE INHIBITING COMPOUNDS

A compound of the formula: STR1 is disclosed as an HIV protease inhibitor. Methods and compositions for inhibiting an HIV infection are also disclosed.