Nicolai Cramer
Cramer, Nicolai 1977-
Cramer, N.
Cramer, N. (Nicolai)
Cramer, Nikolai, Chemist
VIAF ID: 312881921 (Personal)
Permalink: http://viaf.org/viaf/312881921
Preferred Forms
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100 1 _ ‡a Cramer, N.
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100 1 _ ‡a Cramer, N. ‡q (Nicolai)
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100 1 _ ‡a Cramer, Nicolai ‡d 1977-
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100 0 _ ‡a Nicolai Cramer
4xx's: Alternate Name Forms (5)
5xx's: Related Names (4)
- 510 2 _
‡a
Institute of Chemical Sciences and Engineering (Lausanne)
- 510 2 _
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Institute of Chemical Sciences and Engineering
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Lausanne
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affi
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https://d-nb.info/standards/elementset/gnd#affiliation
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Affiliation
- 510 2 _
‡a
Springer-Verlag (Berlin)
- 551 _ _
‡a
Stuttgart
‡4
ortg
‡4
https://d-nb.info/standards/elementset/gnd#placeOfBirth
Works
Title | Sources |
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The 44 th EUCHEMS Conference on Stereochemistry (Bürgenstock Conference 2009) |
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The 4th Young Faculty Meeting - Science and Funding in its Different Varieties. |
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Aromatic homologation by non-chelate-assisted Rh(III)-catalyzed C-H functionalization of arenes with alkynes |
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Asymmetric Alkenyl C-H Functionalization by Cpx RhIII forms 2H-Pyrrol-2-ones through [4+1]-Annulation of Acryl Amides and Allenes |
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Asymmetric synthesis of isoindolones by chiral cyclopentadienyl-rhodium |
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Biomimetic synthesis of (+)-ledene, (+)-viridiflorol, (-)-palustrol, (+)-spathulenol, and psiguadial A, C, and D via the platform terpene (+)-bicyclogermacrene |
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C-C bond activation |
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Catalysis: Gold unleashes the power of three. |
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Catalytic asymmetric functionalization of inert bonds and synthesis of bioactive natural products |
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Catalytic enantioselective reductive Eschenmoser-Claisen rearrangements |
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Catalytic Enantioselective Transformations Involving C-H Bond Cleavage by Transition-Metal Complexes. |
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Chiral 1,3,2-Diazaphospholenes as Catalytic Molecular Hydrides for Enantioselective Conjugate Reductions. |
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Chiral Cp-rhodium(III)-catalyzed asymmetric hydroarylations of 1,1-disubstituted alkenes. |
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Chiral cyclopentadienyl ligands as stereocontrolling element in asymmetric C-H functionalization. |
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Chiral monodentate phosphines and bulky carboxylic acids: cooperative effects in palladium-catalyzed enantioselective C(sp3)-H functionalization |
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Concise total synthesis of (+/-)-marcfortine B. |
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Cooperative Effects between Chiral Cpx -Iridium |
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Cyclobutanes in catalysis |
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Cylindramid und Tropane: von der Naturstoffsynthese zur Synthese mit Naturstoffen |
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Diaminophosphine oxide ligand enabled asymmetric nickel-catalyzed hydrocarbamoylations of alkenes |
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Divergent Synthesis of Densely Substituted Arenes and Pyridines via Cyclotrimerization Reactions of Alkynyl Triazenes |
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Efficient Kinetic Resolution of Sulfur-Stereogenic Sulfoximines by Exploiting CpX RhIII -Catalyzed C-H Functionalization |
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Enantioselective Access to 1H-Isoindoles with Quaternary Stereogenic Centers by Palladium |
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Enantioselective Access to S-Chiral 1,2-Benzothiazines by CpxRh(III) Catalyzed C-H Functionalization of Sulfoximines |
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Enantioselective assembly of the benzo[d]xanthene tetracyclic core of anti-influenza active natural products |
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Enantioselective C-H arylation strategy for functionalized dibenzazepinones with quaternary stereocenters. |
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Enantioselective C-H Functionalization-Addition Sequence Delivers Densely Substituted 3-Azabicyclo[3.1.0]hexanes. |
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Heteroatom-nucleophile-induced C-C fragmentations: synthesis of allenes and entry to domino reactions |
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Highly enantioselective rhodium |
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Intermolecular Palladium(0)-Catalyzed Atropo-enantioselective C-H Arylation of Heteroarenes |
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Iridium-catalyzed acid-assisted asymmetric hydrogenation of oximes to hydroxylamines |
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Ligand-controlled regiodivergent pathways of rhodium(III)-catalyzed dihydroisoquinolone synthesis: experimental and computational studies of different cyclopentadienyl ligands. |
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Mild complexation protocol for chiral CpRh and Ir complexes suitable for catalysis |
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Neutral chiral cyclopentadienyl Ru(ii)Cl catalysts enable enantioselective [2+2]-cycloadditions |
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Nickel-Catalyzed Enantioselective Pyridone C-H Functionalizations Enabled by a Bulky N-Heterocyclic Carbene Ligand |
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Palladium-catalyzed arylative ring-opening reactions of norbornenols: entry to highly substituted cyclohexenes, quinolines, and tetrahydroquinolines |
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Preparation of UDP-galacturonic acid using UDP-sugar pyrophosphorylase |
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Regiodivergent cyclobutanone cleavage: switching selectivity with different Lewis acids |
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Rhodium-catalyzed C-C bond cleavage: construction of acyclic methyl substituted quaternary stereogenic centers. |
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Rhodium-catalyzed dynamic kinetic asymmetric transformations of racemic allenes by the [3+2] annulation of aryl ketimines |
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Rhodium(III)-Catalyzed Enantiotopic C-H Activation Enables Access to P-Chiral Cyclic Phosphinamides. |
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Rhodium(III)/copper(II)-promoted trans-selective heteroaryl acyloxylation of alkynes: stereodefined access to trans-enol esters |
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syn-Selective rhodium(I)-catalyzed allylations of ketimines proceeding through a directed C-H activation/allene addition sequence |
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Synthesis of Fijiolide A via an Atropselective Paracyclophane Formation. |
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Synthesis of functionalized spiroindolines via palladium-catalyzed methine C-H arylation |
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TADDOL-based phosphorus(III)-ligands in enantioselective Pd(0)-catalysed C-H functionalisations |
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Tailored trisubstituted chiral Cp x RhIII catalysts for kinetic resolutions of phosphinic amides. |
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Teaching enantioselectivity to C-H bond functionalizations: initial steps of a rather long shot. |
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Total synthesis and NMR investigations of cylindramide |
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A β-Carbon elimination strategy for convenient in situ access to cyclopentadienyl metal complexes. |
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