About: Stereoselective Synthesis ofmyo-Inositol via Ring-Closing Metathesis: A Building Block for Glycosylphosphatidylinositol (GPI) Anchor Synthesis

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About: Stereoselective Synthesis ofmyo-Inositol via Ring-Closing Metathesis: A Building Block for Glycosylphosphatidylinositol (GPI) Anchor Synthesis Goto Sponge NotDistinct Permalink

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scientific article published on 01 April 2002

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 2002 (uk) im April 2002 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'abril de 2002 (ast) scientific article published on 01 April 2002 (en)
publication date	wds:Q57369032-BC2BA73D-6153-49D8-B4C5-866AB583BE1A
publication date	2002-04-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57369032-52BCDB1E-9F91-4FB5-A653-BA6516B8C272
language of work or name	English
cites work	wds:Q57369032-00C3992C-86A0-49E7-94E2-3D84335823EA wds:Q57369032-071B6F42-B863-4A26-A899-580D83AC2E3E wds:Q57369032-23D2EE52-40CE-4E9D-AE77-E4F4FC01DEA8 wds:Q57369032-2D1D8FF8-FE9A-45F0-A1B9-66122C5CF0A1 wds:Q57369032-3FBC9E59-4C5A-4D90-B881-925F18253CF4 wds:Q57369032-55005BBD-91E0-4CB4-8F96-C9EE58D5B6B9 wds:Q57369032-551539A7-5695-4BAE-A488-F67D3FFCB5B7 wds:Q57369032-6A880BCB-F5B9-4F4F-BB34-C835CA58C715 wds:Q57369032-70542141-9DB6-4295-9606-E6A2BC7F5B85 wds:Q57369032-799A34EF-947C-406B-953E-F110FD180B0E wds:Q57369032-7CE2B1E0-7383-4670-9B6E-DA89A11C5A28 wds:Q57369032-7D1462CE-EFB6-478F-82F1-C0A0A90452B0 wds:Q57369032-7D5D6E37-8179-4EDE-8218-C4B82E9FFBB5 wds:Q57369032-80A8E457-E002-42E0-8FDE-05BBD811146A wds:Q57369032-8D89BFD7-71DE-478E-B10B-482F17306630 wds:Q57369032-B23FF8DE-503C-416A-BBEF-61FC03DAD5CC wds:Q57369032-E14DAE31-08A2-43E8-AA79-717A1BD357F9 wds:Q57369032-E3D30F52-0A2D-4460-B74C-5AA10101788A wds:Q57369032-E990C07E-1270-4D1A-B068-B2CB695AC7E0 wds:Q57369032-FE8353AF-B886-411E-AF8F-BC237FB20179
cites work	Cholesterol and sphingolipid enhance the Triton X-100 insolubility of glycosylphosphatidylinositol-anchored proteins by promoting the formation of detergent-insoluble ordered membrane domains High-resolution FRET microscopy of cholera toxin B-subunit and GPI-anchored proteins in cell plasma membranes Lipid domain structure of the plasma membrane revealed by patching of membrane components Functional rafts in cell membranes GPI-anchored proteins and glycoconjugates segregate into lipid rafts in Kinetoplastida The structure, biosynthesis and function of glycosylated phosphatidylinositols in the parasitic protozoa and higher eukaryotes CD1d-restricted immunoglobulin G formation to GPI-anchored antigens mediated by NKT cells Spontaneous incorporation of the glycosyl-phosphatidylinositol-linked protein Thy-1 into cell membranes Synthesis and activity of a new generation of ruthenium-based olefin metathesis catalysts coordinated with 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene ligands Possible roles of glycosphingolipids in lipid rafts. Microdomains in lymphocyte signalling: beyond GPI-anchored proteins Both sphingolipids and cholesterol participate in the detergent insolubility of alkaline phosphatase, a glycosylphosphatidylinositol-anchored protein, in mammalian membranes. Acyl and alkyl chain length of GPI-anchors is critical for raft association in vitro Rapid Assembly of Oligosaccharides: Total Synthesis of a Glycosylphosphatidylinositol Anchor of Trypanosoma brucei Glycosyl Inositol Derivatives Related to Inositolphosphoglycan Mediators: Synthesis, Structure, and Biological Activity Preparation and structure-activity relationship of novel P1/P1'-substituted cyclic urea-based human immunodeficiency virus type-1 protease inhibitors The conversion of carbohydrate derivatives into functionalized cyclohexanes and cyclopentanes Novel synthesis of enantiomerically pure natural inositols and their diastereoisomers Membrane-Permeant 3-OH-Phosphorylated Phosphoinositide Derivatives Synthesis of a close analog of the repeating unit of the antifreeze glycoproteins of polar fish
author name string	wds:Q57369032-3192C9EB-2B14-4B3A-B92D-FF09ACB807A7 wds:Q57369032-84AB881E-3B4A-45C4-B088-F1DABDA01257
author name string	Rosemary M Conrad Michael J Grogan
rdfs:label	Stereoselective Synthesis ofmyo-Inositol via Ring-Closing Metathesis: A Building Block for Glycosylphosphatidylinositol (nl) Stereoselective Synthesis ofmyo-Inositol via Ring-Closing Metathesis: A Building Block for Glycosylphosphatidylinositol (GPI) Anchor Synthesis (en)
skos:prefLabel	Stereoselective Synthesis ofmyo-Inositol via Ring-Closing Metathesis: A Building Block for Glycosylphosphatidylinositol (nl) Stereoselective Synthesis ofmyo-Inositol via Ring-Closing Metathesis: A Building Block for Glycosylphosphatidylinositol (GPI) Anchor Synthesis (en)
name	Stereoselective Synthesis ofmyo-Inositol via Ring-Closing Metathesis: A Building Block for Glycosylphosphatidylinositol (nl) Stereoselective Synthesis ofmyo-Inositol via Ring-Closing Metathesis: A Building Block for Glycosylphosphatidylinositol (GPI) Anchor Synthesis (en)
author	wds:Q57369032-37AF15C7-B2DB-4F99-BFDE-246C290E2BA4
author	Carolyn Bertozzi
title	wds:Q57369032-A165CA36-25CA-4BA6-A4B1-CE4EC8E84285
title	Stereoselective synthesis of myo-inositol via ring-closing metathesis: a building block for glycosylphosphatidylinositol (GPI) anchor synthesis (en)
page(s)	wds:Q57369032-C6E5E8C7-A073-4D82-837C-7B6657802193
page(s)	1359-1361
instance of	wds:Q57369032-ABA33F29-3D4F-4EA6-939E-31EE6E8C48B6
instance of	scholarly article
main subject	wds:Q57369032-DEAB11B4-94D1-4B48-AE73-441F77BAE75E
main subject	stereoselectivity
PubMed ID	wds:Q57369032-125BA582-EBE5-45A2-B119-DBE107DDDBAC
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11950362
PubMed ID	11950362
published in	wds:Q57369032-2A80ACF0-6542-4F32-8286-065772467BF5
published in	Organic Letters
issue	wds:Q57369032-70175221-7FD5-4729-8F81-D542E122E0BA
volume	wds:Q57369032-9CB87627-5C52-4B66-994F-CD4D695FC371
issue	8
volume	4
DOI	wds:Q57369032-E57C3CA5-AF1E-4A79-A68D-8A5E57D4AF85
DOI	http://dx.doi.org/10.1021/OL025680K
DOI	10.1021/OL025680K
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57369032
is cites work of	The structure and mechanism of myo-inositol-1-phosphate synthase. Stereoselective α-glycosylation of C(6)-hydroxyl myo-inositols via nickel catalysis-application to the synthesis of GPI anchor pseudo-oligosaccharides. A concise synthetic route to the conduritols from pentoses Application of the Quiral Program to the Challenge of Myoinositol Synthesis Synthesis of mycobacterial triacylated phosphatidylinositol dimannoside containing an acyl lipid chain at 3-O of inositol Studies into the stereoselectivity of tartrate-derived dienophiles Common-Intermediate Strategy for Synthesis of Conduritols and Inositols via β-Hydroxy Cyclohexenylsilanes A C2-symmetric chiral pool-based flexible strategy: synthesis of (+)- and (-)-shikimic acids, (+)- and (-)-4-epi-shikimic acids, and (+)- and (-)-pinitol. A powerful reagent for synthesis of Weinreb amides directly from carboxylic acids Efficient syntheses of chiral myo-inositol derivatives--key intermediates in glycosylphosphatidylinositol (GPI) syntheses Enantio- and Diastereodivergent Synthetic Route to Multifarious Cyclitols from D-Xylose via Ring-Closing Metathesis. Regioselective Protection and Deprotection of Inositol Hydroxyl Groups Metal trifluoromethanesulfonate-catalyzed regioselective acylation of myo-inositol 1,3,5-orthoformate Chemical Synthesis of GPI Anchors and GPI-Anchored Molecules Ferrier Carbocyclization-Mediated Synthesis of Enantiopure Azido Inositol Analogues Synthesis and characterization of covalent mimics of phosphatidylinositol-4,5-bisphosphate micelles
is cites work of	wds:Q46788829-B72AFFC6-D610-4D92-A337-8C2A4C7AEE32

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