149953-08-2

Upstream product

• 149859-24-5 <1R-(1α,2α,3α)>-1--N-(p-methoxybenzyl)hydroxycarboxamido>-3-(2-propyl)cyclopropane-2-carboxaldehyde 
• 105-13-5 4-Methoxybenzyl alcohol 
• 149859-31-4 <1R-(1α,2α,3α)>-2-(hydroxymethyl)-1--N-(p-methoxybenzyl)hydroxycarboxamido>-3-(2-propyl)cyclopropane 
• 149859-29-0 4-methyl-2(Z)-pentenyl diazoacetate 
• 149859-30-3 (1R-(1α,5α,6α))-6-(2-propyl)-3-oxabicyclo[3.1.0]hexan-2-one 
• 5555-64-6 N-(p-methoxybenzyl)-O-(p-methoxybenzyl)hydroxylamine 
• 21038-22-2 O-(4-methoxybenzyl)hydroxylamine 
• 82290-65-1 (Z)-4-methylpent-2-en-1-ol 

Downstream Products

• 149891-77-0 <1R-(1α,2β,3α)>-1--N-(p-methoxybenzyl)hydroxycarboxamido>-3-(2-propyl)cyclopropane-2-carboxylic acid 
• 149859-26-7 N-<(1R-(1α,2β,3α))-1--N'-(p-methoxybenzyl)hydroxycarboxamido>-3-(2-propyl)-2-cyclopropanoyl>-O-methyl-L-tyrosine-N-methylamide 

Relevant academic research and scientific papers

CYCLOPROPANES AS CONFORMATIONALLY RESTRICTED PEPTIDE ISOSTERES. DESIGN AND SYNTHESIS OF NOVEL COLLAGENASE INHIBITORS

The 1,2,3-trisubstituted cyclopropane derivatives 9 and 10 were prepared as conformationally constrained analogues of the known collagenase inhibitor 8.The syntheses of 9 and 10 featured the highly enantioselective Rh24 catalyzed cyclization of th