876760-57-5

Basic information

• Product Name: (1S,7R)-10,10-Dimethyl-3-(toluene-4-sulfonyl)-3,4-diaza-tricyclo[5.2.1.0^1,5]dec-4-en-2-one
• Synonyms: (1S,7R)-10,10-Dimethyl-3-(toluene-4-sulfonyl)-3,4-diaza-tricyclo[5.2.1.0^1,5]dec-4-en-2-one
• CAS NO: 876760-57-5
• Molecular Weight: 332.423
• Mol File: 876760-57-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,7R)-10,10-Dimethyl-3-(toluene-4-sulfonyl)-3,4-diaza-tricyclo[5.2.1.0^1,5]dec-4-en-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,7R)-10,10-Dimethyl-3-(toluene-4-sulfonyl)-3,4-diaza-tricyclo[5.2.1.0^1,5]dec-4-en-2-one(876760-57-5)
• EPA Substance Registry System: (1S,7R)-10,10-Dimethyl-3-(toluene-4-sulfonyl)-3,4-diaza-tricyclo[5.2.1.0^1,5]dec-4-en-2-one(876760-57-5)

Safety Data

• Hazardous Substances Data: 876760-57-5(Hazardous Substances Data)

Upstream product

• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 464-78-8 (1S)-(+)-ketopinic acid 
• 876760-56-4 2-(2-tosylhydrazono)-7,7-dimethylbicyclo[2.2.1]heptane-1-carboxylic acid 

Downstream Products

• 876760-62-2 1-(1-Acetyl-1H-indol-3-yl)-2-[(1S,5R,7R)-10,10-dimethyl-2-oxo-3-(toluene-4-sulfonyl)-3,4-diaza-tricyclo[5.2.1.0^1,5]dec-4-yl]-ethane-1,2-dione 
• 876760-60-0 1-[(1S,5R,7R)-10,10-Dimethyl-2-oxo-3-(toluene-4-sulfonyl)-3,4-diaza-tricyclo[5.2.1.0^1,5]dec-4-yl]-2-phenyl-ethane-1,2-dione 
• 876760-61-1 1-[(1S,5R,7R)-10,10-Dimethyl-2-oxo-3-(toluene-4-sulfonyl)-3,4-diaza-tricyclo[5.2.1.0^1,5]dec-4-yl]-2-thiophen-2-yl-ethane-1,2-dione 
• 876760-63-3 1-[(1S,5R,7R)-10,10-Dimethyl-2-oxo-3-(toluene-4-sulfonyl)-3,4-diaza-tricyclo[5.2.1.0^1,5]dec-4-yl]-butane-1,2-dione 
• 876760-58-6 (1S,5R,7R)-10,10-Dimethyl-3-(toluene-4-sulfonyl)-3,4-diaza-tricyclo[5.2.1.0^1,5]decan-2-one 

Relevant articles and documents

Diastereoselective allylation of α-ketoamides bearing camphor N-tosylpyrazolidinone auxiliary: Efficient synthesis of highly optically active two stereoisomers

Complementary allylation conditions were developed for the synthesis of both diastereomers of tertiary homoallylic alcohols. Treatment of camphor N-tosylpyrazolidinone derived α-ketoamides with allyltributylstannane afforded both the individual homoallyli