2,3: 5,6-Di-O-isopropylidene-3,5-di-C-methyl-L-mannono-1,4-lactone

被引：6
|
作者：
Booth, Kathrine V.
Jenkinson, Sarah F.
Fleet, George W. J.
Watkin, David J.
机构：
[1] Univ Oxford, Chem Res Lab, Dept Organ Chem, Oxford OX1 3TA, England
[2] Univ Oxford, Chem Res Lab, Dept Chem Crystallog, Oxford OX1 3TA, England
来源：
ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE | 2007年 / 63卷
关键词：
D O I：
10.1107/S1600536807014584
中图分类号：
O7 [晶体学];
学科分类号：
0702 ; 070205 ; 0703 ; 080501 ;
摘要：
The relative configuration at C-2 of the title lactone, C14H22O6, which exists in the five-membered ring form, was unequivocally established by X-ray crystallographic analysis. The absolute configuration was determined by the use of 2,4-di-C-methyl-L-arabinose as the starting material.
引用
收藏
页码：O2204 / O2206
页数：3
相关论文
共 50 条
  • [1] 3,5-Di-C-methyl-5,6-O-isopropylidene-L-mannono-1,4-lactone
    Booth, Kathrine V.
    Jenkinson, Sarah F.
    Fleet, George J. W.
    Watkin, David J.
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2007, 63 : O2427 - O2429
  • [2] An efficient synthesis of L-allono-1,4-lactone from 2,3:5,6-di-O-isopropylidene-D-mannono-1,4-lactone
    Shih, TL
    Tseng, JH
    TETRAHEDRON LETTERS, 2004, 45 (08) : 1789 - 1791
  • [3] 3,5-Di-C-methyl-5,6-O-isopropylidene-L-glucono-1,4-lactone
    Booth, Kathrine V.
    Jenkinson, Sarah F.
    Fleet, George W. J.
    Watkin, David J.
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2007, 63 : O2424 - O2426
  • [4] 5,6-O-isopropylidene-3-C-methyl-D-mannono-1,4-lactone
    Curran, Louise A.
    Jones, Nigel A.
    Jenkinson, Sarah F.
    Watkin, David J.
    Fleet, George W. J.
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2007, 63 : O3416 - U2605
  • [5] 2,3:5,6-di-O-isopropylidene-2-C-hydroxy-methyl-D-talono-1,4-lactone
    Shallard-Brown, HA
    Harding, CC
    Watkin, DJ
    Soengas, R
    Skytte, UP
    Fleet, GWJ
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2004, 60 : O2163 - O2164
  • [6] 2-C-Benzyloxymethyl-2,3:5,6-di-O-isopropylidene-D-allono-1,4-lactone
    Watkin, DJ
    Parry, LL
    Soengas, R
    Izumori, K
    Fleet, GWJ
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2005, 61 : O2955 - O2957
  • [7] HYDROXYMETHYLATION OF 2,3-5,6-DI-O-ISOPROPYLIDENE-D-MANNONO-1,4-LACTONE - SYNTHESIS OF D-MANNO-HEPTULOSE
    KAMPF, A
    DIMANT, E
    CARBOHYDRATE RESEARCH, 1974, 32 (02) : 380 - 382
  • [8] SYNTHESIS OF C-GLYCOSYL COMPOUNDS .1. REACTION OF ETHYL ISOCYANOACETATE WITH 2,3=5,6-DI-O-ISOPROPYLIDENE-D-MANNONO-1,4-LACTONE
    HALL, RH
    BISCHOFBERGER, K
    EITELMAN, SJ
    JORDAAN, A
    JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1977, (07): : 743 - 753
  • [9] 2,2':5,6-Di-O-isopropylidene-2-C-hydroxy-methyl-D-talono-1,4-lactone
    Harding, CC
    Watkin, DJ
    Cowley, AR
    Soengas, R
    Skytte, UP
    Fleet, GWJ
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2005, 61 : O250 - O252
  • [10] Interaction of Reformatskii modified reagent with 2,3-5,6-di-O-cyclohexylidene-D-mannono-1,4-lactone
    Shchepelev, AN
    Beluzhenko, OV
    Kornilov, VI
    Zhdanov, YA
    ZHURNAL OBSHCHEI KHIMII, 1996, 66 (11): : 1933 - 1934
12345