1156540-73-6

Upstream product

• 100-42-5 styrene 
• 147666-20-4 succinimidyl diazoacetate 

Downstream Products

• 1156540-88-3 (1R,2R)-morpholino(2-phenylcyclopropyl)methanone 
• 58641-87-5 (1R,2R)-trans-2-phenylcyclopropane-1-carboxamide 
• 1156540-94-1 N-((1R,2R)-2-phenylcyclopropylcarbonyl)-α-D-glucosamine 
• 1240350-17-7 (1R,2R)-N-((R)-1-hydroxy-3-methylbutan-2-yl)-2-phenylcyclopropanecarboxamide 
• 1156540-92-9 (S)-2-(2-(2-((1R,2R)-2-phenylcyclopropanecarboxamido)acetamido)acetamido)propanoic acid 
• 1156540-85-0 (1R,2R)-N-hexyl-2-phenylcyclopropanecarboxamide 
• 1156540-90-7 (1R,2R)-N-((S)-1-hydroxy-3-phenylpropan-2-yl)-2-phenylcyclopropanecarboxamide 
• 1156540-89-4 methyl (2S)-3-phenyl-2-((1R,2R)-2-phenylcyclopropanecarboxamido)propanoate 
• 1156540-86-1 (1R,2R)-N-(4-methoxyphenyl)-2-phenylcyclopropanecarboxamide 

Relevant academic research and scientific papers

Highly stereoselective Ru(ii)-Pheox catalyzed asymmetric cyclopropanation of terminal olefins with succinimidyl diazoacetate

The Ru(ii)-Pheox complex is an efficient catalyst for the intermolecular cyclopropanation of various terminal olefins with succinimidyl diazoacetate. This catalytic system can perform under mild conditions, and the desired cyclopropane products are obtain

ASYMMETRIC CYCLOPROPANATION WITH SUCCINIMIDYL DIAZOACETATE

Cobalt(ll) complexes of the D2-symmetric chiral porphyrins are effective catalysts for asymmetric cyclopropanation reactions with succinimidyl diazoacetate. The Co-catalyzed reaction is suitable for various olefins, providing the corresponding cyclopropane succinimidyl esters in high yields and excellent diastereo- and enantio-selectivity. The resulting enantioenriched cyclopropane succinimidyl esters can serve as convenient synthons for the general synthesis of optically active cyclopropyl carboxamides through mild reactions with a wide range of amine derivatives, including unprotected peptides and amino sugars

Asymmetric Co(II)-catalyzed cyclopropanation with succinimidyl diazoacetate: General synthesis of chiral cyclopropyl carboxamides

[Co(P1)] is an effective catalyst for asymmetric cyclopropanation with succinimidyl diazoacetate. The Co(II)-catalyzed reaction is suitable for various olefins, providing the desired cyclopropane succinimidyl esters in high yields and excellent diastereo-