Lehnhoff, Stefan, Goebel, Matthias, Karl, Rosa Maria, Klösel, Roland, Ugi, Ivar (1995) Stereoselektive Synthesen von Peptidderivaten mit 2-Acetamido-3,4,6-tri-O-acetyl-1-amino-2-desoxy-β-D-glucopyranose durch Vierkomponentenkondensation. Angewandte Chemie, 107 (10). 1208-1211 doi:10.1002/ange.19951071017

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Reference Type	Journal (article/letter/editorial)
Title	Stereoselektive Synthesen von Peptidderivaten mit 2-Acetamido-3,4,6-tri-O-acetyl-1-amino-2-desoxy-β-D-glucopyranose durch Vierkomponentenkondensation
Journal	Angewandte Chemie
Authors	Lehnhoff, Stefan		Author
	Goebel, Matthias		Author
	Karl, Rosa Maria		Author
	Klösel, Roland		Author
	Ugi, Ivar		Author
Year	1995 (May 15)	Volume	107
Issue	10
Publisher	Wiley
DOI	doi:10.1002/ange.19951071017Search in ResearchGate
	Generate Citation Formats
Mindat Ref. ID	7291741	Long-form Identifier	mindat:1:5:7291741:9
GUID	0
Full Reference	Lehnhoff, Stefan, Goebel, Matthias, Karl, Rosa Maria, Klösel, Roland, Ugi, Ivar (1995) Stereoselektive Synthesen von Peptidderivaten mit 2-Acetamido-3,4,6-tri-O-acetyl-1-amino-2-desoxy-β-D-glucopyranose durch Vierkomponentenkondensation. Angewandte Chemie, 107 (10). 1208-1211 doi:10.1002/ange.19951071017
Plain Text	Lehnhoff, Stefan, Goebel, Matthias, Karl, Rosa Maria, Klösel, Roland, Ugi, Ivar (1995) Stereoselektive Synthesen von Peptidderivaten mit 2-Acetamido-3,4,6-tri-O-acetyl-1-amino-2-desoxy-β-D-glucopyranose durch Vierkomponentenkondensation. Angewandte Chemie, 107 (10). 1208-1211 doi:10.1002/ange.19951071017
In	(1995, May) Angewandte Chemie Vol. 107 (10) Wiley

	OGURI, S., TEJIMA, S. (1981) ChemInform Abstract: A NEW SYNTHESIS OF 2-ACETAMIDO-4-O-(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-β-D-GLUCOPYRANOSYL# )-1,3,6-TRI-O-ACETYL-2-DEOXY-α-D-GLUCOPYRANOSE (CHITOBIOSE OCTAACETATE) Chemischer Informationsdienst, 12 (21) doi:10.1002/chin.198121342
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	ANTONENKO, T. S., ZURABJAN, S. E., CHORLIN, A. JA. (1970) ChemInform Abstract: HERST. VON 2-O-(2-ACETAMIDO-2-DESOXY-BETA-D-GLUCOPYRANOSYL)-GLYCERIN UND 2-ACETAMIDO-3-O-(2-ACETAMIDO-2-DESOXY-BETA-D-GLUCOPYRANOSYL)-2-DESOXY-D-GLUCOPYRANOSE NACH DER OXAZOLIN-METHODE. Chemischer Informationsdienst. Organische Chemie, 1. doi:10.1002/chin.197037388
	KOTO, S., MORISHIMA, N., SATO, H., SATO, Y., ZEN, S. (1985) ChemInform Abstract: SYNTHESIS OF O-β-D-GLUCOPYRANOSYL-(1 → 2)-O-β-D-GLUCOPYRANOSYL-(1 → 6)-D-GLUCOPYRANOSE; DEHYDRATIVE β-D-GLUCOSYLATION USING 2-O-ACETYL-3,4,6-TRI-O-BENZYL-D-GLUCOPYRANOSE. Chemischer Informationsdienst, 16 (29) doi:10.1002/chin.198529337
	Stein, Andreas, Kula, Maria-Regina, Elling, Lothar, Verseck, Stefan, Klaffke, Werner (1995) Synthesen von dTDP-6-Desoxy-4-ketoglucose und deren Analoga mit nativer und rekombinanter dTDP-Glucose-4,6-dehydratase. Angewandte Chemie, 107 (16). 1881-1883 doi:10.1002/ange.19951071615
	*Dömling, Alexander, Starnecker, Manfred, Ugi, Ivar (1995) β-Lactam-Nucleosid-Chimäre. Angewandte Chemie, 107 (20). 2465-2467 doi:10.1002/ange.19951072031*
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	Cherevatskaya, Maria, Neumann, Matthias, Füldner, Stefan, Harlander, Christoph, Kümmel, Susanne, Dankesreiter, Stephan, Pfitzner, Arno, Zeitler, Kirsten, König, Burkhard (2012) Stereoselektive Alkylierung mit sichtbarem Licht durch Kombination von heterogener Photokatalyse mit Organokatalyse. Angewandte Chemie, 124 (17). 4138-4142 doi:10.1002/ange.201108721
	Koto, Shinkiti, Morishima, Naohiko, Sato, Hiroko, Sato, Yuko, Zen, Shonosuke (1985) Synthesis ofO-β-D-Glucopyranosyl-(1→2)-O-β-D-glucopyranosyl-(1→6)-D-glucopyranose; Dehydrative β-D-Glucosylation Using 2-O-Acetyl-3,4,6-tri-O-benzyl-D-glucopyranose. Bulletin of the Chemical Society of Japan, 58 (1). 120-122 doi:10.1246/bcsj.58.120
	Bolli, Martin, Leumann, Christian (1995) Tripelhelixbildung von Oligonucleotiden mit [(3′S,5′R)-2′-Desoxy-3′,5′-ethano-β-D-ribofuranosyl]nucleosid(„Bicyclodesoxynucleosid”)-Bausteinen. Angewandte Chemie, 107 (6). 740-742 doi:10.1002/ange.19951070622
	Schwerdtfeger, Jörg, Hoppe, Dieter (1992) Stereoselektive Erzeugung von 1-Acyloxy-2-amino-Carbanionen durch Deprotonierung; Synthese von enantio- und diastereomerenreinen β-Aminoalkoholen. Angewandte Chemie, 104 (11). 1547-1549 doi:10.1002/ange.19921041137

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