반응 #569389

ord-fd907b13486c4e71af8262b14973c3b2

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The reaction was quenched by addition of 2 volumes of acetone
  2. 2
    기타The precipitated protein was removed by centrifugation
  3. 3
    기타After removal of the solvent under reduced pressure

실험 절차

The acceptor aldehyde, 3-thioglyceraldehyde (Compound 3), was prepared by the method of Effenberger. [Effenberger Tetrahedron Lett., 33:5157 (1992)]. DERA (400U) was added to a 10 mL solution containing the acceptor aldehyde (100 mM Compound 3) and donor aldehyde (300 mM acetaldehyde), triethanolamine buffer (100 mM, pH 7.3) and EDTA (1 mM). This reaction is shown in Scheme 1. The resulting solution was stirred in the dark for 2 days under a N2 atmosphere. The reaction was quenched by addition of 2 volumes of acetone and cooling to 0° C. for 20 minutes. The precipitated protein was removed by centrifugation. After removal of the solvent under reduced pressure, a 33 percent yield of Compound 4 was obtained (characterized as 2-deoxy-5-thio-1,3,4-tri-O-acetyl-D-erythro-pentose). Compound 4 was purified from the residue by preparative TLC on silica (methanol/chloroform/hexane, 1:90:10).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05795749uspto-grants-1998_08