860617-73-8

Basic information

• Product Name: N-[(1S)-1-(1-benzenesulfonyl-3,4-dihydroxycyclopentylmethyl)-2-(1-methyl-1H-indol-3-yl)ethyl]-4-methylbenzenesulfonamide
• Synonyms: N-[(1S)-1-(1-benzenesulfonyl-3,4-dihydroxycyclopentylmethyl)-2-(1-methyl-1H-indol-3-yl)ethyl]-4-methylbenzenesulfonamide
• CAS NO: 860617-73-8
• Molecular Weight: 582.742
• Mol File: 860617-73-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-[(1S)-1-(1-benzenesulfonyl-3,4-dihydroxycyclopentylmethyl)-2-(1-methyl-1H-indol-3-yl)ethyl]-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(1S)-1-(1-benzenesulfonyl-3,4-dihydroxycyclopentylmethyl)-2-(1-methyl-1H-indol-3-yl)ethyl]-4-methylbenzenesulfonamide(860617-73-8)
• EPA Substance Registry System: N-[(1S)-1-(1-benzenesulfonyl-3,4-dihydroxycyclopentylmethyl)-2-(1-methyl-1H-indol-3-yl)ethyl]-4-methylbenzenesulfonamide(860617-73-8)

Safety Data

• Hazardous Substances Data: 860617-73-8(Hazardous Substances Data)

Upstream product

• 860438-74-0 N-[(1S)-1-(1-benzenesulfonylcyclopent-3-enylmethyl)-2-(1-methyl-1H-indol-3-yl)ethyl]-4-methylbenzenesulfonamide 
• 21339-55-9 1-methyl-L-tryptophan 
• 860438-73-9 1-methyl-3-[(2S)-1-(toluene-4-sulfonyl)aziridin-2-ylmethyl]-1H-indole 

Downstream Products

• 860438-75-1 (1S,12S)-3-methyl-14-[[phenylsulfonyl]-18-oxoethyl]-16-(toluene-4-sulfonyl)-3,16-diazatetracyclo[10.3.1.0^2,10.0^4,9]hexadeca-2⁽¹⁰⁾,4,6,8-tetraene 

Relevant articles and documents

4-(Phenylsulfonyl)-4-lithiocyclopentene as a nucleophilic 2-pentene-1,5-dial synthetic equivalent. An aziridine-based synthetic approach to (-)-alstonerine

Reaction of 4-lithio-4-(phenylsulfonyl)cyclopentene with an l-tryptophan-derived N-tosylaziridine provides an adduct. Oxidative cleavage of the cyclopentene double bond provides a dialdehyde, which enters into acid-catalysed Pictet-Spengler-type bicyclisation to give a tetracyclic aldehyde. Completely regioselective silyl dienol ether formation followed by completely stereoselective hetero-Diels-Alder reaction with monomeric formaldehyde gives a late-stage intermediate in a planned total synthesis of the macroline-related alkaloid (-)-alstonerine.