1365533-56-7

Basic information

• Product Name: (S)-2-(((tert-butyldimethylsilyl)oxy)methyl)-1-tosylindoline
• Synonyms: (S)-2-(((tert-butyldimethylsilyl)oxy)methyl)-1-tosylindoline
• CAS NO: 1365533-56-7
• Molecular Weight: 417.645
• Mol File: 1365533-56-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-(((tert-butyldimethylsilyl)oxy)methyl)-1-tosylindoline(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-(((tert-butyldimethylsilyl)oxy)methyl)-1-tosylindoline(1365533-56-7)
• EPA Substance Registry System: (S)-2-(((tert-butyldimethylsilyl)oxy)methyl)-1-tosylindoline(1365533-56-7)

Safety Data

• Hazardous Substances Data: 1365533-56-7(Hazardous Substances Data)

Upstream product

• 938069-18-2 2-bromo-L-phenylalanine methyl ester 
• 1365533-54-5 (S)-methyl 3-(2-bromophenyl)-2-(p-toluenylsulfonamido)propanoate 
• 1365533-55-6 (S)-N-(1-(2-bromophenyl)-3-((tert-butyldimethylsilyl)oxy)propan-2-yl)-p-toluenesulfonamide 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant articles and documents

Asymmetric induction in domino Heck-aza-Michael reactions

Domino Heck-aza-Michael reactions are an efficient method for the rapid synthesis of functionalised N-heterocycles. An asymmetric version of this domino process has been developed to access chiral 1,3-disubstituted N-heterocycles from amino acid precursors in excellent yields (68-81%) with moderate to high diastereoselectivity (up to 92% de).