About: “Marking” the nitrogen atoms of phenyl-(2-pyridyl)-(3-pyridyl)-(4-pyridyl)-methane. Synthesis and absolute configuration of the corresponding tris(pyridine N-oxide)

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About: “Marking” the nitrogen atoms of phenyl-(2-pyridyl)-(3-pyridyl)-(4-pyridyl)-methane. Synthesis and absolute configuration of the corresponding tris(pyridine N-oxide) Goto Sponge NotDistinct Permalink

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scientific article published on 26 May 2011

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description	wetenschappelijk artikel (nl) bài báo khoa học (vi) наукова стаття, опублікована в травні 2011 (uk) article scientifique publié en 2011 (fr) im Mai 2011 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 26 May 2011 (en) artículu científicu espublizáu en mayu de 2011 (ast) 2011 മെയ് 26 നു പ്രസിദ്ധീകരിച്ച ശാസ്ത്ര ലേഖനം (ml)
publication date	wds:Q57555177-380DD93A-7A55-401D-B68A-EA198D41B016
publication date	2011-05-26 00:00:00Z (xsd:dateTime)
cites work	wds:Q57555177-0E7EFC6E-C33F-443A-8C99-2139C063E8B6 wds:Q57555177-10DD1161-047A-4E8E-93A2-02D0DF816517 wds:Q57555177-131B7C40-8FED-4411-AFF6-31B52159BF4B wds:Q57555177-1B9F828D-944D-4943-ABD8-F32B1A9C74DD wds:Q57555177-1EDACB25-37BE-4387-BAC1-5C2FD485FA2F wds:Q57555177-24959C2F-80C2-4046-8D01-158D0D4A099B wds:Q57555177-33638F2F-00E4-4A22-B9B8-BCA309AE595B wds:Q57555177-366A2A12-187A-48E0-BDE4-8EC44A67A26D wds:Q57555177-3AE0F6B9-ACA0-4DCD-8C72-FCB7F05A2B25 wds:Q57555177-5388C9F8-49AF-4112-8869-BE81B9278203 wds:Q57555177-5699ED03-F7D2-46EF-90E3-B1AAC25777F7 wds:Q57555177-65CCD95E-B095-49D0-B5E8-B532333A1593 wds:Q57555177-69D51F75-0AF7-4A3C-BE8C-F3FBC3E23527 wds:Q57555177-6F312C0D-EB62-4B62-A47F-F7C0E1DA49DC wds:Q57555177-70D63042-34BC-4BF4-AAD9-76B0582E74BA wds:Q57555177-72CC5F68-8CFD-4EF8-BFF0-ED5B7F575318 wds:Q57555177-8013CD29-28EA-4E86-8D6C-CBA9C575C809 wds:Q57555177-95718A6B-6B86-406D-8F5B-8643E6FD3AFF wds:Q57555177-A0F893ED-2CA5-49AE-A509-8C93790EB31B wds:Q57555177-A32D5ECB-0B40-4333-8F04-0134186BAE50 wds:Q57555177-A765B05D-72E3-4338-AB30-5F8A45AB0CBA wds:Q57555177-AEC87910-F094-4E79-BA6F-73A0975B23BA wds:Q57555177-B809E89A-339C-44B2-B84F-0F50ED9B14DA wds:Q57555177-BECCC83E-6452-4D15-85BC-D6EAA1336F01 wds:Q57555177-C8E8D424-2EA6-43A9-8006-703BF2F482E4 wds:Q57555177-CBFC79EB-71AB-4A18-BAD1-764AB02B70AD wds:Q57555177-CCE45776-405D-495B-9006-BE2B23927843 wds:Q57555177-D1FA224B-D9B4-4E4F-90B8-73158F0843B1 wds:Q57555177-D4650A07-82EE-4ACE-B60A-6C863B4AEDBB wds:Q57555177-DFF3FEE1-B73B-4739-A5D6-148185977DAA wds:Q57555177-E77AAF64-B011-4E89-A0E5-20F9099228BD wds:Q57555177-EE43E00B-1A8E-4773-968B-A7C6F5757CA8 wds:Q57555177-FA610C4D-BE9F-4E44-A3C0-7C3DDAAB7615 wds:Q57555177-FF0846A5-395F-4E7A-B246-6FE933EFD852 wds:Q57555177-FF149909-F982-4391-93E5-23A9CECC681D
cites work	The use of X-ray crystallography to determine absolute configuration Density-functional thermochemistry. III. The role of exact exchange Crystallographic evidence for the existence of CH...O, CH...N and CH...Cl hydrogen bonds Merck molecular force field. I. Basis, form, scope, parameterization, and performance of MMFF94 Application of electronic circular dichroism in configurational and conformational analysis of organic compounds Trityl ethers: molecular bevel gears reporting chirality through circular dichroism spectra. BINOL: a versatile chiral reagent C3 Symmetry in Asymmetric Catalysis and Chiral Recognition Hydrogen-bond control in axially chiral styrenes: selective synthesis of enantiomerically pure C2-symmetric paracyclophanes Enantioselective synthesis of silanol. Synthesis and properties of allenic natural products and pharmaceuticals An enantiomerically pure alleno-acetylenic macrocycle: synthesis and rationalization of its outstanding chiroptical response. Single-reference ab initio methods for the calculation of excited states of large molecules Metal−Bis(helicene) Assemblies Incorporating π-Conjugated Phosphole-Azahelicene Ligands: Impacting Chiroptical Properties by Metal Variation [2.2]Paracyclophane derivatives in asymmetric catalysis Computing chiroptical properties with first-principles theoretical methods: background and illustrative examples 6-31G* basis set for third-row atoms Absolute structural elucidation of natural products--a focus on quantum-mechanical calculations of solid-state CD spectra Absolute configuration of chirally deuterated neopentane Spiro skeletons: a class of privileged structure for chiral ligand design. [123]Tetramantane: parent of a new family of sigma-helicenes Development of Chiral Spiro Ligands for Metal-Catalyzed Asymmetric Reactions Chirality in the Absence of Rigid Stereogenic Elements: The Absolute Configuration of Residual Enantiomers ofC3-Symmetric Propellers Functionalized chiral ionic liquids: a new type of asymmetric organocatalysts and nonclassical chiral ligands Enantioselective and catalytic method for alpha-crotylation of aldehydes with a kinetic self-refinement of stereochemistry Chiral (2,5)pyrido[7(4)]allenoacetylenic cyclophanes: synthesis and characterization A chiral concave-bound cyclopentadienyl iron complex of sumanene. 1,1′-Bi(trishomobarrelenyl) - Synthesis and Chiroptic Properties Helical chiral pyridine N-oxides: a new family of asymmetric catalysts Preparation of C(3)-symmetric homochiral syn-trisnorbornabenzenes through regioselective cyclotrimerization of enantiopure iodonorbornenes. Axially chiral binaphthyl surrogates with an inner N-H-N hydrogen bond. Mixed electric-magnetic second-order nonlinear optical response of helicenes Enantiopure anthrylene-ethynylene cyclic tetramer and racemization via rotation of anthracene unit about acetylenic axes Phenyl-(2-pyridyl)-(3-pyridyl)-(4-pyridyl)methane: synthesis, chiroptical properties, and theoretical calculation of its absolute configuration Noncovalent interactions in the asymmetric synthesis of rigid, conjugated helical structures
author name string	wds:Q57555177-0769E55B-B92F-4854-8B12-D61762A4C17C wds:Q57555177-63B9653A-B172-4CA1-9CE5-8F68E879C318
author name string	Takuya Inagaki Kaori Miki
rdfs:label	“Marking” the nitrogen atoms of phenyl-(2-pyridyl)-(3-pyridyl)-(4-pyridyl)-methane. Synthesis and absolute configuration of the corresponding tris(pyridine N-oxide) (en) “Marking” the nitrogen atoms of phenyl- (nl)
skos:prefLabel	“Marking” the nitrogen atoms of phenyl-(2-pyridyl)-(3-pyridyl)-(4-pyridyl)-methane. Synthesis and absolute configuration of the corresponding tris(pyridine N-oxide) (en) “Marking” the nitrogen atoms of phenyl- (nl)
name	“Marking” the nitrogen atoms of phenyl-(2-pyridyl)-(3-pyridyl)-(4-pyridyl)-methane. Synthesis and absolute configuration of the corresponding tris(pyridine N-oxide) (en) “Marking” the nitrogen atoms of phenyl- (nl)
author	wds:Q57555177-64BACC6B-D413-4BE2-A66F-270EBDC5B132 wds:Q57555177-81DBA48C-1098-4B61-9CE4-90CF8435695A wds:Q57555177-84A7212C-92B5-430D-A48A-F4FF6140A703 wds:Q57555177-BB705A40-A8F0-4173-A177-EE8F3C0E6806 wds:Q57555177-D573BAAC-19DA-4597-B4B2-CB5B3B7ED230 wds:Q57555177-DCAC8F28-4303-47CD-A48A-4C2438B1B415 wds:Q57555177-E78BB5C8-1331-44AC-B876-B04469CB15F8
author	Tatsuo Nehira Gennaro Pescitelli

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