Synthesis of a ribofuranosyl cation mimic

被引：35

作者：

Bols, M ^{[1
]}

机构：

[1] TECH UNIV DENMARK,DEPT ORGAN CHEM,DK-2800 LYNGBY,DENMARK

来源：

关键词：

D O I：

10.1016/0040-4039(96)00202-X

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

(3S,4S)-3,4-dihydroxy-3-hydroxymethylpyrrolidine was prepared and found to be a transitionstate analogue for beta-D-ribofuranosyl cleavage.

引用

页码：2097 / 2100

页数：4

共 9 条

[1] Halvorson H., 1966, Methods in Enzymology, V8, P559, DOI 10.1016/0076-6879(66)08101-1
[2] BRANCHED-CHAIN SUGARS REACTION OF FURANOSES WITH FORMALDEHYDE - SIMPLE SYNTHESIS OF D-APIOSE AND L-APIOSE
HO, PT
[J]. CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1979, 57 (04): : 381 - 383
[3] Hughes N.A., 1965, CARBOHYD RES, V1, P176, DOI DOI 10.1016/S0008-6215(00)80921-0
[4] FACILE SYNTHESIS OF GLUCOSE-TYPE 1-N-IMINOSUGARS - NEW INHIBITOR OF GLYCOLIPID BIOSYNTHESIS
ICHIKAWA, M
IGARASHI, Y
ICHIKAWA, Y
[J]. TETRAHEDRON LETTERS, 1995, 36 (11) : 1767 - 1770
[5] AN EXTREMELY POTENT INHIBITOR FOR BETA-GALACTOSIDASE
ICHIKAWA, Y
IGARASHI, Y
[J]. TETRAHEDRON LETTERS, 1995, 36 (26) : 4585 - 4586
[6] ISOFAGOMINE, A POTENT, NEW GLYCOSIDASE INHIBITOR
JESPERSEN, TM
DONG, WL
SIERKS, MR
SKRYDSTRUP, T
LUNDT, I
BOLS, M
[J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1994, 33 (17): : 1778 - 1779
[7] RAYMOND JL, 1991, ANGEW CHEM, V103, P1690
[8] Schmidt O.T., 1963, METHODS CARBOHYDRATE, V2, P318
[9] Stoeckler J D, 1978, Methods Enzymol, V51, P530