Works matching Johann Joachim Becher
Results: 579
Hans Egede (1686–1758) and the alchemical tradition in Denmark-Norway.
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- Science in Context (0269-8897), 2019, v. 32, n. 3, p. 285, doi. 10.1017/S0269889719000267
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Seckendorff as an Economist in Comparison with Contemporary Writers.
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- European Journal of Law & Economics, 2005, v. 19, n. 3, p. 235, doi. 10.1007/s10657-005-6635-9
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The "Subtile Aereal Spirit of Fountains": Mineral Waters and the History of Pneumatic Chemistry.
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- Early Science & Medicine, 2016, v. 21, n. 4, p. 303, doi. 10.1163/15733823-00214p02
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Scientific Revolutions: Paradigm Shifts.
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- Lapham's Quarterly, 2014, v. 7, n. 2, p. 12
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Partial wave analysis of ψ3686→ΛΣ¯0π0 + c.c.
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- Journal of High Energy Physics, 2025, v. 2025, n. 2, p. 1, doi. 10.1007/JHEP02(2025)212
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Partial wave analysis of ψ3686→ΛΣ¯0π0 + c.c.
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- Journal of High Energy Physics, 2025, v. 2025, n. 2, p. 1, doi. 10.1007/JHEP02(2025)212
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Biologization of Allogeneic Bone Grafts with Polyphosphate: A Route to a Biomimetic Periosteum.
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- Advanced Functional Materials, 2019, v. 29, n. 44, p. N.PAG, doi. 10.1002/adfm.201905220
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The Evolution of Hemocyanin Genes in Caenogastropoda: Gene Duplications and Intron Accumulation in Highly Diverse Gastropods.
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- Journal of Molecular Evolution, 2021, v. 89, n. 9/10, p. 639, doi. 10.1007/s00239-021-10036-y
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Hemocyanins of Muricidae: New 'Insights' Unravel an Additional Highly Hydrophilic 800 kDa Mass Within the Molecule.
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- Journal of Molecular Evolution, 2021, v. 89, n. 1/2, p. 62, doi. 10.1007/s00239-020-09986-6
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Pathologie im Zeitalter der Gewalt: Mainz 1916 bis 1946.
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- Der Pathologe, 2019, v. 40, p. 288, doi. 10.1007/s00292-019-00701-x
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Bemerkung zu Einem Vergleichssatz für Gewöhnliche Lineare Differentialgleichungen.
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- Manuscripta Mathematica, 1972, v. 7, n. 1, p. 83, doi. 10.1007/BF01303538
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Integraltransformationen zu Singulären S-Hermiteschen Rand-Eigenwertproblemen.
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- Manuscripta Mathematica, 1971, v. 5, n. 2, p. 133, doi. 10.1007/BF01325023
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Possible impact of climate change on the occurrence and the epidemic development of cercospora leaf spot disease ( Cercospora beticola sacc.) in sugar beets for Rhineland-Palatinate and the southern part of Hesse.
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- Climatic Change, 2016, v. 137, n. 3/4, p. 481, doi. 10.1007/s10584-016-1697-y
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Tree mixture effects on aboveground nutrient pools of trees in an experimental plantation in Panama.
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- Plant & Soil, 2010, v. 326, n. 1/2, p. 199, doi. 10.1007/s11104-009-9997-x
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Upscaling calcite dissolution rates in a tight reservoir sandstone.
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- Environmental Earth Sciences, 2022, v. 81, n. 11, p. 1, doi. 10.1007/s12665-022-10399-5
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The CLU-files: disentanglement of a mystery.
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- Biomolecular Concepts, 2016, v. 7, n. 1, p. 1, doi. 10.1515/bmc-2015-0026
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A numerical compass for experiment design in chemical kinetics and molecular property estimation.
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- Journal of Cheminformatics, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13321-024-00825-0
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Carbohydrates as Chiral Auxiliaries in Stereoselective Synthesis. New Synthetic Methods (90).
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- Angewandte Chemie International Edition, 1993, v. 32, n. 3, p. 336, doi. 10.1002/anie.199303361
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β-Alkyl and β-Alkyl-α-Hydroxy Carboxylic Acid Derivatives from Radical or Ionic 1,4 Addition of Dialkylaluminum Chlorides to α,β-Unsaturated N-Acyl Urethanes.
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- Angewandte Chemie International Edition, 1991, v. 30, n. 6, p. 694, doi. 10.1002/anie.199106941
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The 3-(3-Pyridyl)allyloxycarbonyl (Paloc) Moiety-a Stable, Amino-Protecting Group for Peptide Syntheses in Organic Media and in Water That Is Cleavable under Neutral Conditions.
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- Angewandte Chemie International Edition, 1990, v. 29, n. 12, p. 1457, doi. 10.1002/anie.199014571
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From the Bicyclo[3.3.0]octane Framework to Multiply Bridged [12]Annulenes and Semibulvanes.
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- Angewandte Chemie International Edition, 1989, v. 28, n. 10, p. 1343, doi. 10.1002/anie.198913431
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Carbohydrates as Chiral Templates: Stereoselective Synthesis of β-Amino Acids.
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- Angewandte Chemie International Edition, 1989, v. 28, n. 8, p. 1068, doi. 10.1002/anie.198910681
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Carbohydrates as Chiral Templates: Stereoselective Tandem Mannich-Michael Reactions for the Synthesis of Piperidine Alkaloids.
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- Angewandte Chemie International Edition, 1989, v. 28, n. 8, p. 1067, doi. 10.1002/anie.198910671
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Bis-Stilbene Systems: Reduction to the Tetraanions.
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- Angewandte Chemie International Edition, 1989, v. 28, n. 7, p. 904, doi. 10.1002/anie.198909041
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The p-Nitrocinnamyloxycarbonyl (Noc) Moiety-an Acid-stable Amino-protecting Group Removable under Neutral Conditions for Peptide and Glycopeptide Synthesis.
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- Angewandte Chemie International Edition, 1988, v. 27, n. 10, p. 1375, doi. 10.1002/anie.198813751
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(Mesityl)<sub>2</sub>Ge(fluorenylidene)-Stabilization of a Ge-C Double Bond by Charge Transfer into an Aromatic System.
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- Angewandte Chemie International Edition, 1988, v. 27, n. 6, p. 828, doi. 10.1002/anie.198808281
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Amino Acid Methyl Esters as Chiral Auxiliaries in Aza-Diels-Alder Reactions in Aqueous Solution.
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- Angewandte Chemie International Edition, 1988, v. 27, n. 2, p. 274, doi. 10.1002/anie.198802741
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Polystannanes Ph<sub>3</sub>Sn-.
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- Angewandte Chemie International Edition, 1987, v. 26, n. 12, p. 1255, doi. 10.1002/anie.198712551
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A Non-Stereospecific Diels-Alder Reaction.
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- Angewandte Chemie International Edition, 1987, v. 26, n. 10, p. 1046, doi. 10.1002/anie.198710461
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New Reductive Transformations of Unsaturated Cyclic Hydrocarbons [New Synthetic Methods (66)].
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- Angewandte Chemie International Edition, 1987, v. 26, n. 3, p. 204, doi. 10.1002/anie.198702041
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Poly(anthrylenetrimethylene) and 9,10-Bridged Anthracenes by Reductive Alkylation.
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- Angewandte Chemie International Edition, 1986, v. 25, n. 5, p. 444, doi. 10.1002/anie.198604441
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Synthesis and Redox Properties of Compounds with Several Separated Anthracene Electrophores.
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- Angewandte Chemie International Edition, 1986, v. 25, n. 5, p. 443, doi. 10.1002/anie.198604431
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Synthesis of O-Glycopeptides of the Tumor-Associated T<sub>N</sub>- and T-Antigen Type and Their Binding to Bovine Serum Albumin.
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- Angewandte Chemie International Edition, 1986, v. 25, n. 4, p. 360, doi. 10.1002/anie.198603601
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Synthesis of the all- L-Configurated Cyclotetradepsipeptide cyclo[- L-Val- L-Lac-]<sub>2</sub> by the Combined Protection/Activation Method with the 2,4-Bis(methylthio)phenoxycarbonyl Group.
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- Angewandte Chemie International Edition, 1986, v. 25, n. 2, p. 170, doi. 10.1002/anie.198601701
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Photoreactions of N-(1-Pyridinio)amidates in Monolayers and Liposomes.
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- Angewandte Chemie International Edition, 1985, v. 24, n. 10, p. 882, doi. 10.1002/anie.198508821
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Construction of Disaccharide N-Glycopeptides-Synthesis of the Linkage Region of the Transmembrance-Neuraminidase of an Influenza Virus.
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- Angewandte Chemie International Edition, 1985, v. 24, n. 10, p. 883, doi. 10.1002/anie.198508831
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A Nucleolipid with Antiviral Acycloguanosine as Head Group-Synthesis and Liposome Formation.
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- Angewandte Chemie International Edition, 1985, v. 24, n. 6, p. 501, doi. 10.1002/anie.198505011
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2-(Pyridyl)ethyl Esters as Secure yet Readily Removable Polarophilic Carboxy-Protection in Peptide Synthesis.
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- Angewandte Chemie International Edition, 1984, v. 23, n. 9, p. 716, doi. 10.1002/anie.198407161
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Isolation of the ( E)-Enols of β-Ketocarboxylic Acid Derivatives.
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- Angewandte Chemie International Edition, 1985, v. 24, n. 4, p. 350, doi. 10.1002/anie.198503501
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'Dimers' of Aldosterone.
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- Angewandte Chemie International Edition, 1985, v. 24, n. 2, p. 130, doi. 10.1002/anie.198501301
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(C<sub>6</sub>H<sub>5</sub>Sb)<sub>6</sub>·(1,4-dioxane), the First Cyclohexastibane.
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- Angewandte Chemie International Edition, 1985, v. 24, n. 1, p. 72, doi. 10.1002/anie.198500721
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Synthesis of the all- L-Configurated Cyclohexadepsipeptide cyclo-[ L-Val- L-Lac]<sub>3</sub> by the Peoc/Acid Chloride Method.
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- Angewandte Chemie International Edition, 1984, v. 23, n. 10, p. 808, doi. 10.1002/anie.198408081
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The Allyloxycarbonyl (Aloc) Moiety-Conversion of an Unsuitable into a Valuable Amino Protecting Group for Peptide Synthesis.
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- Angewandte Chemie International Edition, 1984, v. 23, n. 6, p. 436, doi. 10.1002/anie.198404361
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Ring Expansion of Benzothiete to 2,3-Dihydrobenz[ d]isothiazoles.
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- Angewandte Chemie International Edition, 1984, v. 23, n. 3, p. 244, doi. 10.1002/anie.198402441
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The Allyl Group as Mildly and Selectively Removable Carboxy-Protecting Group for the Synthesis of Labile O-Glycopeptides.
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- Angewandte Chemie International Edition, 1984, v. 23, n. 1, p. 71, doi. 10.1002/anie.198400711
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O-Glycopeptide Synthesis using 9-Fluorenylmethoxycarbonyl (Fmoc)-Protected Synthetic Units.
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- Angewandte Chemie International Edition, 1983, v. 22, n. 1, p. 62, doi. 10.1002/anie.198300622
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Coupling of Sterically Hindered Peptide Bonds-A Renaissance of the Acid Chloride Method.
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- Angewandte Chemie International Edition, 1982, v. 21, n. 8, p. 630, doi. 10.1002/anie.198206301
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The 1,3-Dithian-2-ylmethoxycarbonyl (Dmoc) Moiety-A Protecting Group for the Amino Function in Peptide Synthesis.
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- Angewandte Chemie International Edition, 1982, v. 21, n. 4, p. 292, doi. 10.1002/anie.198202921
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Der 1,3-Dithian-2-yl-methoxycarbonyl-(Dmoc-) Rest, eine Sicherheitsschutzgruppe für die Aminofunktion bei der Peptid-syntheses.
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- Angewandte Chemie International Edition, 1982, v. 21, n. S4, p. 702, doi. 10.1002/anie.198207020
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Dodecamethyl-1λ<sup>3</sup>,4λ<sup>3</sup>-diphospha-2,3,5,6,7,8-hexastannabicyclo[2.2.2]octane, a Highly Symmetrical Cage Molecule.
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- Angewandte Chemie International Edition, 1981, v. 20, n. 12, p. 1029, doi. 10.1002/anie.198110291
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