1984
DOI: 10.1002/9780470129692.ch4
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The Total Synthesis of Carbohydrates 1972–1980

Abstract: A Route to 3-Deoxy-4-O-methyl-D-manno-oct-2-ulosonic Acid (4-O-Methyl-KDO) and Its D-gluco Isomer Derivatives.-Starting with the gluconic acid derivative (I) via the Barton ester the α,β-unsaturated ketoester (III) is prepared. Its methoxymercuration leads to the title compounds (V) and (VI). -(PAKULSKI

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Cited by 20 publications
(6 citation statements)
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“…A further important result is that the normalization of the main sequence evolves strongly over the redshift range of our sample; the median SFR at fixed M ⋆ evolves downwards by a factor of 3, measured at 10 11 M ⊙ , from the our highest (median z = 0.98) to our lowest (median z = 0.36) redshift bin. Importantly, it appears that the whole of the main sequence shifts downwards with time, rather than just the upper envelope decreasing, which was also reported by a recent GALEX study at z = 0.7 (Zamojski et al 2007). A straightforward interpretation of these observations is that normal star-forming galaxies possess a limited range of SFR at a given M ⋆ and z, which is presumably set by whatever physical processes regulate SF in quiescent disks.…”
Section: Resultssupporting
confidence: 74%
“…A further important result is that the normalization of the main sequence evolves strongly over the redshift range of our sample; the median SFR at fixed M ⋆ evolves downwards by a factor of 3, measured at 10 11 M ⊙ , from the our highest (median z = 0.98) to our lowest (median z = 0.36) redshift bin. Importantly, it appears that the whole of the main sequence shifts downwards with time, rather than just the upper envelope decreasing, which was also reported by a recent GALEX study at z = 0.7 (Zamojski et al 2007). A straightforward interpretation of these observations is that normal star-forming galaxies possess a limited range of SFR at a given M ⋆ and z, which is presumably set by whatever physical processes regulate SF in quiescent disks.…”
Section: Resultssupporting
confidence: 74%
“…The Spitzer-IRAC depths are those expected at 5σ in a 3 ′′ aperture for observations taken in 2006. The GALEX depths are from Zamojski et al (2007). transmission, telescope reflectivity, instrument optical transmission, filter transmission and detector sensitivity are plotted in Figures 1 & 2 in units of relative detector quantum efficiency normalized to 1 at the peak.…”
Section: Observations and Data Reductionmentioning
confidence: 99%
“…The ACS data acquisition and reduction are detailed in Koekemoer et al (2007), and a monochromatic catalog based only on the HST-ACS observations is presented in Leauthaud et al (2007). Observations at other wavelengths consist of: X-ray observations with XMM (Hasinger et al 2007), ultraviolet (UV) observations with GALEX (Zamojski et al 2007), mid-infrared observations with the Spitzer Space Telescope (Sanders et al 2007), sub-mm observations from the Caltech Sub-mm Observatory (CSO) (Aguirre et al 2007) and Institut de Radioastronomie Millimétrique (IRAM) 30m telescope (Bertoldi et al 2007), and radio observations with the Very Large Array (VLA) (Schinnerer et al 2004(Schinnerer et al , 2007.…”
Section: Introductionmentioning
confidence: 99%
“…The optically active S‐enantiomer of 1‐(2‐furyl) ethanol is used as an important building block for the synthesis of various natural products such as flavonoids, polyketide antibiotics, and carbohydrate derivatives . Kobayashi et al reported the enantioselective synthesis of natural product macrosphelides A and B, which act as anti‐adhesion compounds and effectively inhibit the adhesion of human leukemia HL‐60 cells to human‐umbilical‐vein endothelial cells, using S‐1‐(2‐furyl) ethanol as the starting precursor .…”
Section: Introductionmentioning
confidence: 99%
“…12,13 The optically active S-enantiomer of 1-(2-furyl) ethanol is used as an important building block for the synthesis of various natural products such as flavonoids, polyketide antibiotics, and carbohydrate derivatives. [14][15][16] Kobayashi et al reported the enantioselective synthesis of natural product macrosphelides A and B, which act as anti-adhesion compounds and effectively inhibit the adhesion of human leukemia HL-60 cells to human-umbilical-vein endothelial cells, using S-1-(2-furyl) ethanol as the starting precursor. 17 There are a few studies reported on the synthesis of the single enantiomer of 1-(2-furyl) ethanol by asymmetric reduction using baker's yeast, asymmetric chemical catalysts, or lipase-catalyzed kinetic resolution.…”
Section: Introductionmentioning
confidence: 99%