282735-71-1

Basic information

• Product Name: (2'S,3S,4'R,5'R)-1,2-dihydro-2'-(2-methoxy-2-methylpropyl)-2-oxo-5'-[[(2R)-2-[(phenylmethoxy)carbonyl]-1-pyrrolidinyl]carbonyl]spiro[3H-indole-3,3'-pyrrolidine]-4'-carboxylic acid ethyl ester
• Synonyms: (2'S,3S,4'R,5'R)-1,2-dihydro-2'-(2-methoxy-2-methylpropyl)-2-oxo-5'-[[(2R)-2-[(phenylmethoxy)carbonyl]-1-pyrrolidinyl]carbonyl]spiro[3H-indole-3,3'-pyrrolidine]-4'-carboxylic acid ethyl ester
• CAS NO: 282735-71-1
• Molecular Weight: 577.678
• Mol File: 282735-71-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2'S,3S,4'R,5'R)-1,2-dihydro-2'-(2-methoxy-2-methylpropyl)-2-oxo-5'-[[(2R)-2-[(phenylmethoxy)carbonyl]-1-pyrrolidinyl]carbonyl]spiro[3H-indole-3,3'-pyrrolidine]-4'-carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2'S,3S,4'R,5'R)-1,2-dihydro-2'-(2-methoxy-2-methylpropyl)-2-oxo-5'-[[(2R)-2-[(phenylmethoxy)carbonyl]-1-pyrrolidinyl]carbonyl]spiro[3H-indole-3,3'-pyrrolidine]-4'-carboxylic acid ethyl ester(282735-71-1)
• EPA Substance Registry System: (2'S,3S,4'R,5'R)-1,2-dihydro-2'-(2-methoxy-2-methylpropyl)-2-oxo-5'-[[(2R)-2-[(phenylmethoxy)carbonyl]-1-pyrrolidinyl]carbonyl]spiro[3H-indole-3,3'-pyrrolidine]-4'-carboxylic acid ethyl ester(282735-71-1)

Safety Data

• Hazardous Substances Data: 282735-71-1(Hazardous Substances Data)

Upstream product

• 181134-54-3 3-methoxy-3-methylbutanal 
• 91-56-5 indole-2,3-dione 
• 56539-66-3 solfit 
• 282735-67-5 (3S,3'S,4'R,6'S,8'R,8'aR)-1,2,3',4',8',8a'-hexahydro-6'-(2-methoxy-2-methylpropyl)-1',2-dioxo-3',4'-diphenylspiro[3H-indole-3,7'(6'H)-[1H]pyrrolo[2,1-c][1,4]oxazine]-8'-carboxylic acid ethyl ester 
• 21728-28-9 (E)-(2-oxo-1,2-dihydroindol-3-ylidene)acetic acid ethyl ester 
• 64472-06-6 (R)-proline benzyl ester 
• 473896-06-9 (2'S,3'S,4'R,5'R)-2'-(2-Methoxy-2-methyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3'-pyrrolidine]-4',5'-dicarboxylic acid 4'-ethyl ester 

Relevant articles and documents

Asymmetric, stereocontrolled total synthesis of (+) and (-)-spirotryprostatin B via a diastereoselective azomethine ylide [1,3]-dipolar cycloaddition reaction

The asymmetric, stereocontrolled total syntheses of (+) and (-)-spirotryprostatin B (2) are described. Formation of the core pyrrolidine ring was accomplished via a diastereoselective asymmetric [1,3]-dipolar cycloaddition reaction. Addition of 3-methoxy-