934586-58-0

Basic information

• Product Name: methyl 3-(3-(2-methoxy-2-oxoethyl)-2-oxo-1-(2-(1-tosyl-1H-indol-3-yl)acetyl)piperidin-3-yl)-3-oxo-propanoate
• Synonyms: methyl 3-(3-(2-methoxy-2-oxoethyl)-2-oxo-1-(2-(1-tosyl-1H-indol-3-yl)acetyl)piperidin-3-yl)-3-oxo-propanoate
• CAS NO: 934586-58-0
• Molecular Weight: 582.631
• Mol File: 934586-58-0.mol

Chemical Properties

• CAS DataBase Reference: methyl 3-(3-(2-methoxy-2-oxoethyl)-2-oxo-1-(2-(1-tosyl-1H-indol-3-yl)acetyl)piperidin-3-yl)-3-oxo-propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-(3-(2-methoxy-2-oxoethyl)-2-oxo-1-(2-(1-tosyl-1H-indol-3-yl)acetyl)piperidin-3-yl)-3-oxo-propanoate(934586-58-0)
• EPA Substance Registry System: methyl 3-(3-(2-methoxy-2-oxoethyl)-2-oxo-1-(2-(1-tosyl-1H-indol-3-yl)acetyl)piperidin-3-yl)-3-oxo-propanoate(934586-58-0)

Safety Data

• Hazardous Substances Data: 934586-58-0(Hazardous Substances Data)

Upstream product

• 3731-16-6 3-carboethoxy-2-pyridone 
• 128742-77-8 [N-(p-toluenesulfonyl)indol-3-yl]acetic acid 
• 908003-71-4 3-(3-tert-butoxycarbonylmethyl-2-oxo-piperidin-3-yl)-3-oxo-propionic acid methyl ester 
• 908003-70-3 3-tert-butoxycarbonylmethyl-2-oxo-piperidine-3-carboxylic acid ethyl ester 
• 908003-82-7 3-{[(tert-butoxy)carbonyl]methyl}-2-oxopiperidine-3-carboxylic acid 
• 915707-12-9 methyl 3-(3-(2-methoxy-2-oxoethyl)-2-oxo-piperidin-3-yl)-3-oxo-propanoate 
• 915706-91-1 2-(1-tosyl-1H-indol-3-yl)acetyl chloride 

Downstream Products

• 934586-53-5 methyl 2-diazo-3-(3-(2-methoxy-2-oxoethyl)-2-oxo-1-(2-(1-tosyl-1H-indol-3-yl)acetyl)piperidin-3-yl)-3-oxo-propanoate 

Relevant articles and documents

A dipolar cycloaddition approach toward the kopsifoline alkaloid framework

Using a metal-catalyzed domino reaction as the key step, the heterocyclic skeleton of the kopsifoline alkaloid family was constructed by a 1,3-dipolar cycloaddition of a carbonyl ylide dipole derived from a Rh(II)-catalyzed reaction of a diazo ketoester across the indole π-bond. Ring opening of the resulting 1,3-dipolar cycloadduct followed by a reductive dehydroxylation step resulted in the formation of a critical silyl enol ether necessary for the final F-ring closure of the kopsifoline skeleton.

Cycloaddition protocol for the assembly of the hexacyclic framework associated with the kopsifoline alkaloids

(Chemical Equation Presented) An approach to the hexacyclic framework of the kopsifoline alkaloids has been developed and is based on a Rh(II)-catalyzed cyclization-cycloaddition cascade. The resulting [3+2]-cycloadduct was readily converted into the TBS