1327157-88-9

Basic information

• Product Name: C₂₁H₂₅NO₆S
• Synonyms: C₂₁H₂₅NO₆S
• CAS NO: 1327157-88-9
• Molecular Weight: 419.499
• Mol File: 1327157-88-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₁H₂₅NO₆S(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₁H₂₅NO₆S(1327157-88-9)
• EPA Substance Registry System: C₂₁H₂₅NO₆S(1327157-88-9)

Safety Data

• Hazardous Substances Data: 1327157-88-9(Hazardous Substances Data)

Upstream product

• 196090-72-9 Toluene-4-sulfonic acid (S)-(R)-1-(1,4-dioxa-spiro[4.5]dec-2-yl)-but-3-enyl ester 
• 98-59-9 p-toluenesulfonyl chloride 
• 200499-58-7 (R)-1-benzyloxycarbonyl-2-[(S)-1,2-dihydroxyethyl]pyrrolidine 
• 1327157-89-0 C₂₀H₂₇NO₄ 
• 1013212-24-2 (1R)-1-[(2S)-1,4-dioxaspiro[4.5]dec-2-yl]-3-butenyl azide 

Downstream Products

• 741703-35-5 phenylmethyl (2R,2'S)-2-(oxiran-2-yl)pyrrolidine-1-carboxylate 
• 1327157-87-8 (R)-benzyl 2-((R)-1-hydroxypent-4-en-1-yl)pyrrolidine-1-carboxylate 
• 1327157-86-7 C₁₆H₂₃NO₄ 
• 1327157-90-3 C₂₃H₂₉NO₆S 

Relevant articles and documents

Stereoselective synthesis of (+)-(8R,8aR)-perhydro-8-indolizidinol

A highly stereoselective total synthesis of (+)-(8R,8aR)-perhydro-8- indolizidinol is described. Key steps involved in this synthesis are diastereoselective zinc allylation, azido-olefin cyclization and reductive amination followed by cyclization which effectively constructed the indolizidine ring. This contributes a unique approach to the synthesis of indolizidine alkaloids that offers the advantages of brevity and relatively high overall yields.