76490-22-7

Usage

InChI:InChI=1/C20H33N5O11/c1-9(23-17(31)10(2)26)16(30)25-13(20(35)36)6-7-14(27)24-12(18(32)22-8-15(28)29)5-3-4-11(21)19(33)34/h9-13,26H,3-8,21H2,1-2H3,(H,22,32)(H,23,31)(H,24,27)(H,25,30)(H,28,29)(H,33,34)(H,35,36)/t9-,10+,11+,12+,13?/m0/s1

Upstream product

• 76490-23-8 (2R,6S)-6-{(R)-4-[(S)-2-((R)-2-Acetoxy-propionylamino)-propionylamino]-4-carboxy-butyrylamino}-2-amino-6-(carboxymethyl-carbamoyl)-hexanoic acid 
• 76490-23-8 (2S,6S)-6-{(R)-4-[(S)-2-((R)-2-Acetoxy-propionylamino)-propionylamino]-4-carboxy-butyrylamino}-2-amino-6-(carboxymethyl-carbamoyl)-hexanoic acid 
• 80162-37-4 (S)-4-[(1S,5R)-5-Amino-1-(carboxymethyl-carbamoyl)-5-hydrazinocarbonyl-pentylcarbamoyl]-2-[(S)-2-((R)-2-hydroxy-propionylamino)-propionylamino]-butyric acid 
• 76490-19-2 D-lactoyl(OAc)-L-Ala-γ-L-Glu(α-OBzl)-(L)-Boc-(D)meso-A₂pm(D)-NHNHBoc-(L)-Gly 
• 80162-38-5 C₂₂H₄₃N₅O₈Si 
• 80162-37-4 (R)-4-[(1S,5R)-5-Amino-1-(carboxymethyl-carbamoyl)-5-hydrazinocarbonyl-pentylcarbamoyl]-2-[(S)-2-((S)-2-hydroxy-propionylamino)-propionylamino]-butyric acid 
• 76490-19-2 L-lactoyl(OAc)-L-Ala-γ-D-Glu(α-OBzl)-(L)-Boc-(D)meso-A₂pm(D)-NHNHBoc-(L)-Gly 
• 80162-37-4 (R)-4-[(1S,5R)-5-Amino-1-(carboxymethyl-carbamoyl)-5-hydrazinocarbonyl-pentylcarbamoyl]-2-[(R)-2-((R)-2-hydroxy-propionylamino)-propionylamino]-butyric acid 
• 76490-19-2 D-lactoyl(OAc)-D-Ala-γ-D-Glu(α-OBzl)-(L)-Boc-(D)meso-A₂pm(D)-NHNHBoc-(L)-Gly 
• 76490-23-8 (2S,6R)-6-{(R)-4-[(S)-2-((R)-2-Acetoxy-propionylamino)-propionylamino]-4-carboxy-butyrylamino}-2-amino-6-(carboxymethyl-carbamoyl)-hexanoic acid 
• 80162-37-4 (R)-4-[(1S,5R)-5-Amino-1-(carboxymethyl-carbamoyl)-5-hydrazinocarbonyl-pentylcarbamoyl]-2-[(S)-2-(2-hydroxy-propionylamino)-propionylamino]-butyric acid 
• 76489-90-2 (2S,6R)-2-Benzyloxycarbonylamino-6-tert-butoxycarbonylamino-7-(N'-tert-butoxycarbonyl-hydrazino)-7-oxo-heptanoic acid 
• 76489-82-2 (2S,6R)-2,6-Diamino-7-(N'-tert-butoxycarbonyl-hydrazino)-7-oxo-heptanoic acid 
• 80162-36-3 Boc-L-alanyl-D-glutamic acid 

Relevant academic research and scientific papers

AN EFFICIENT METHOD FOR SELECTIVE AMINO ACID PROTECTION OF meso-2,2'-DIAMINODICARBOXYLIC ACID: AN IMPROVED SYNTHESIS OF FK-156

An efficient method for selective amino acid protection with proper differentiation between the two amino acid groups in meso-2,2'-diaminopimelic acid has been achieved (7 -> 8 -> 9 -> 10 -> 11) and applied to the synthesis of FK-156 (10 -> 12 -> 14 -> 1)