17554-22-2Relevant academic research and scientific papers
Phosphorus pentoxide for amide and peptide bond formation with minimal by-products
Erapalapati, Venkataramana,Hale, Umatai A.,Madhavan, Nandita
supporting information, (2019/11/21)
Phosphorus pentoxide and DMAP are used for amide bond formation from carboxylic acids and amines. Dipeptides and amides have been synthesized using this reagent in 42–77% yields and >99% ees. The protocol is attractive as it occurs at ambient temperature, the formation of organic by-products is minimal and the reagent can be readily quenched using water. Furthermore, excellent enantioselectivities are observed without the use of harsh triazole based additives.
Practical Peptide Synthesis Mediated by a Recyclable Hypervalent Iodine Reagent and Tris(4-methoxyphenyl)phosphine
Zhang, Chi,Liu, Shan-Shan,Sun, Bo,Tian, Jun
supporting information, p. 4106 - 4109 (2015/09/01)
6-(3,5-Bis(trifluoromethyl)phenyl)-1H,4H-2aλ3-ioda-2,3-dioxacyclopenta[hi]indene-1,4-dione (p-BTFP-iodosodilactone, 1a) was synthesized and demonstrated to be an efficient hypervalent iodine(III) reagent for the synthesis of dipeptides from various standard amino acids, including sterically hindered amino acids, in good to high yields within 30 min in the presence of tris(4-methoxyphenyl)phosphine. In addition, the combined system of 1a/(4-MeOC6H4)3P was used to synthesize the pentapeptide leu-enkephalin in protected form. It is worth noting that 1a can be regenerated readily after reaction.
ONE-STEP STEREOSPECIFIC SYNTHESIS OF α,β-DEHYDROAMINO ACIDS AND DEHYDROPEPTIDES
Berti, Federico,Ebert, Cynthia,Gardossi, Lucia
, p. 8145 - 8148 (2007/10/02)
Dehydroamino acids and dehydropeptides were prepared by a one-pot reaction employing diethyl chlorophosphate in the presence of sodium hydride.The reaction is stereospecific and proceeds without racemization.
