93417-23-3

Upstream product

• 93417-22-2 C₃₀H₄₂O₇ 

Downstream Products

• 93528-31-5 (4S,14S)-(-)-4,14-diphenyl-3,6,9,12,15-pentaoxa-21-azabicyclo<15.3.1>heneicosa-1(21),17,19-triene-2,16-dione 
• 93600-90-9 (4S,14S)-(-)-4,14-diphenyl-3,6,9,12,15,20-hexaoxabicyclo<15.2.1>eicosa-17,19-diene-2,16-dione 
• 93527-96-9 (4S,14S)-(+)-4,14-diphenyl-1,4,7,10,13,16-hexaoxacyclooctadecane-2,16-dione 
• 189451-77-2 (4S,14S)-19,21-Dimethoxy-4,14-diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17⁽²¹⁾,18-triene 
• 189451-78-3 (4S,14S)-19-Bromo-21-methoxy-4,14-diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17⁽²¹⁾,18-triene 
• 857682-68-9 3,3-Bis-((4S,14S)-21-allyloxy-4,14-diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17⁽²¹⁾,18-trien-19-yl)-3H-isobenzofuran-1-one 
• 189451-75-0 (4S,14S)-4,14-Diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17⁽²¹⁾,18-trien-21-ol 
• 189451-80-7 (4S,14S)-4,14-Diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17-diene-19,21-dione 
• 189451-74-9 (4S,14S)-19-Bromo-4,14-diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17⁽²¹⁾,18-trien-21-ol 
• 189451-76-1 (4S,14S)-19-Methoxy-4,14-diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17⁽²¹⁾,18-trien-21-ol 
• 189451-79-4 (4S,14S)-21-Methoxy-4,14-diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17⁽²¹⁾,18-triene 
• 189451-81-8 (4S,14S)-19-Bromo-21-methoxymethoxy-4,14-diphenyl-3,6,9,12,15-pentaoxa-bicyclo[15.3.1]henicosa-1⁽²⁰⁾,17⁽²¹⁾,18-triene 

Relevant academic research and scientific papers

Preparation of homochiral phenolic crown ethers containing para-substituted phenol moiety and chiral subunits derived from (S)-1-phenylethane-1,2-diol: Their chiral recognition behaviour in complexation with neutral amines

Crown ethers 1-6 containing two chiral subunits derived from (S)-1-phenylethane-1, 2-diol and a phenol moiety bearing an intra-annular OH group and an additional para-substituent have been prepared in enantiomerically pure forms and their enantiomer recog

The Preparation of New Chiral Diphenyl-Substituted Macrocyclic Polyether-Diester Compounds and their Enantiomeric Recognition of Chiral Organic Ammonium Salts

A series of chiral diphenyl-substituted macrocyclic polyether-diester ligands have been prepared from the chiral diphenyl-substituted tetraethylene glycol.Enantiomeric recognition by the chiral diphenyl-sunstituted pyridino-diester-18-crown-6 compound (7)