UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Selective Carbon-Carbon Bond Cleavage of Cyclopropylamine Derivatives

Chemical reviews, 2021-01, Vol.121 (1), p.80-109

2021

Volltextzugriff (PDF)

Stereocontrolled Synthesis of Fluorinated Isochromans via Iodine(I)/Iodine(III) Catalysis

Angewandte Chemie International Edition, 2022-07, Vol.61 (30), p.e202205277-n/a

International ed. in English, 2022

Volltextzugriff (PDF)

Branch-Selective Alkene Hydroarylation by Cooperative Destabilization: Iridium-Catalyzed ortho-Alkylation of Acetanilides

Angewandte Chemie (International ed.), 2015-12, Vol.54 (49), p.14866-14870

International ed. in English, 2015

Volltextzugriff (PDF)

An endo‐Directing‐Group Strategy Unlocks Enantioselective (3+1+2) Carbonylative Cycloadditions of Aminocyclopropanes

Angewandte Chemie International Edition, 2022-08, Vol.61 (32), p.e202205007-n/a

International ed. in English, 2022

Volltextzugriff (PDF)

Biochemical Properties of a Promising Milk-Clotting Enzyme, Moose (Alces alces) Recombinant Chymosin

Foods, 2023-10, Vol.12 (20), p.3772

2023

Volltextzugriff (PDF)

Carbonylative C–C Bond Activation of Aminocyclopropanes Using a Temporary Directing Group Strategy

Journal of the American Chemical Society, 2020-11, Vol.142 (45), p.19006-19011

2020

Volltextzugriff (PDF)

Modular Access to Eight‐Membered N‐Heterocycles by Directed Carbonylative C−C Bond Activation of Aminocyclopropanes

Angewandte Chemie International Edition, 2019-12, Vol.58 (52), p.18844-18848

International ed. in English, 2019

Volltextzugriff (PDF)

An endo‐Directing‐Group Strategy Unlocks Enantioselective (3+1+2) Carbonylative Cycloadditions of Aminocyclopropanes

Angewandte Chemie, 2022-08, Vol.134 (32), p.n/a

2022

Volltextzugriff (PDF)

Stereokontrollierte Synthese von fluorierten Isochromanen durch Iod(I)/Iod(III)‐Katalyse

Angewandte Chemie, 2022-07, Vol.134 (30), p.n/a

2022

Volltextzugriff (PDF)

Branch-Selective Alkene Hydroarylation by Cooperative Destabilization: Iridium-Catalyzed ortho-Alkylation of Acetanilides

Angewandte Chemie, 2015-12, Vol.127 (49), p.15079-15083

2015

Volltextzugriff (PDF)

Fast highly efficient 'on-solvent' non catalytic cascade transformation of benzaldehydes and 4-hydroxycoumarin into bis(4-hydroxycoumarinyl)arylmethanes

ARKIVOC free online journal of organic chemistry, 2017-05, Vol.2017 (3), p.121-129

2017

Volltextzugriff (PDF)

Electrocatalytic Cascade Reaction of Aldehydes and 4-Hydroxy-6-methyl-2H-pyran-2-one

Electrocatalysis, 2018-09, Vol.9 (5), p.602-607

2018

Volltextzugriff (PDF)

Catalyst-free tandem Knoevenagel-Michael reaction of aldehydes and pyrazolin-5-one: fast and convenient approach to medicinally relevant 4,4′-(arylmethylene)bis(1H-pyrazol-5-ol)s

Heterocyclic communications, 2015-04, Vol.21 (2), p.97-101

2015

Volltextzugriff (PDF)

Modular Access to Eight‐Membered N‐Heterocycles by Directed Carbonylative C−C Bond Activation of Aminocyclopropanes

Angewandte Chemie, 2019-12, Vol.131 (52), p.19020-19024

2019

Volltextzugriff (PDF)

C–C Bond Activations of Minimally Activated Cyclopropanes

Synlett, 2022-11, Vol.34 (12), p.1317-1326

2022

Volltextzugriff (PDF)

Efficient non-catalytic synthesis of substituted 2,3,4,9-tetrahydro-1H-xanthen-1-ones from salicylaldehydes and dimedone

Mendeleev communications, 2015-01, Vol.25 (1), p.19-20

2015

Volltextzugriff (PDF)

A Comparison of the Dynamics of S100B, S100A1, and S100A6 mRNA Expression in Hippocampal CA1 Area of Rats during Long-Term Potentiation and after Low-Frequency Stimulation

Cardiovascular Psychiatry and Neurology, 2010, Vol.2010 (2010), p.1-6

2010

Volltextzugriff (PDF)

Electrocatalysis in MIRC reaction strategy: facile stereoselective approach to medicinally relevant spirocyclopropylbarbiturates from barbituric acids and activated olefins

RSC advances, 2012-01, Vol.2 (10), p.4444

2012

Volltextzugriff (PDF)

Non-catalytic multicomponent rapid and efficient approach to 10-(2,4,6-trioxohexahydropyrimidin-5-yl)-3,3-dimethyl-2,3,4,9-tetrahydro-1H-xanthen-1-ones from salicylaldehydes, dimedone, and barbituric acids

Monatshefte für Chemie, 2015-10, Vol.146 (10), p.1689-1694

2015

Volltextzugriff (PDF)

Stereoselective synthesis of medicinally relevant furo[2,3-d]pyrimidine framework by thermal rearrangement of spirocyclic barbiturates

RSC advances, 2015, Vol.5 (115), p.94986-94989

2015

Volltextzugriff (PDF)

ChemInform Abstract: Branch‐Selective Alkene Hydroarylation by Cooperative Destabilization: Iridium‐Catalyzed ortho‐Alkylation of Acetanilides

ChemInform, 2016-03, Vol.47 (15), p.no-no

2016

Volltextzugriff (PDF)

ChemInform Abstract: Stereoselective Synthesis of Medicinally Relevant Furo[2,3‐d]pyrimidine Framework by Thermal Rearrangement of Spirocyclic Barbiturates

ChemInform, 2016-03, Vol.47 (12), p.no-no

2016

Volltextzugriff (PDF)

ChemInform Abstract: Non‐catalytic Multicomponent Rapid and Efficient Approach to 10‐(2,4,6‐Trioxohexahydropyrimidin‐5‐yl) ‐3,3‐dimethyl‐2,3,4,9‐tetrahydro‐1H‐xanthen‐1‐ones from Salicylaldehydes, Dimedone, and Barbituric Acids

ChemInform, 2016-03, Vol.47 (14), p.no-no

2016

Volltextzugriff (PDF)

Stereoselective synthesis of medicinally relevant furo[2,3-d]pyrimidine framework by thermal rearrangement of spirocyclic barbituratesElectronic supplementary information (ESI) available. CCDC 1423220. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5ra19169f

2015-11

Volltextzugriff (PDF)

ChemInform Abstract: Efficient Non-Catalytic Synthesis of Substituted 2,3,4,9-Tetrahydro-1H-xanthen-1-ones from Salicylaldehydes and Dimedone

ChemInform, 2015-06, Vol.46 (24), p.no-no

2015

Volltextzugriff (PDF)

1 – 25 von 113

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(96)
Mit Volltextzugriff
(90)

Publikationsform

Sprache

Englisch
(110)
Japanisch
(11)
Russisch
(11)
Spanisch
(2)
Deutsch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Selective Carbon-Carbon Bond Cleavage of Cyclopropylamine Derivatives

Stereocontrolled Synthesis of Fluorinated Isochromans via Iodine(I)/Iodine(III) Catalysis

Branch-Selective Alkene Hydroarylation by Cooperative Destabilization: Iridium-Catalyzed ortho-Alkylation of Acetanilides

An endo‐Directing‐Group Strategy Unlocks Enantioselective (3+1+2) Carbonylative Cycloadditions of Aminocyclopropanes

Biochemical Properties of a Promising Milk-Clotting Enzyme, Moose (Alces alces) Recombinant Chymosin

Carbonylative C–C Bond Activation of Aminocyclopropanes Using a Temporary Directing Group Strategy

Modular Access to Eight‐Membered N‐Heterocycles by Directed Carbonylative C−C Bond Activation of Aminocyclopropanes

An endo‐Directing‐Group Strategy Unlocks Enantioselective (3+1+2) Carbonylative Cycloadditions of Aminocyclopropanes

Stereokontrollierte Synthese von fluorierten Isochromanen durch Iod(I)/Iod(III)‐Katalyse

Branch-Selective Alkene Hydroarylation by Cooperative Destabilization: Iridium-Catalyzed ortho-Alkylation of Acetanilides

Fast highly efficient 'on-solvent' non catalytic cascade transformation of benzaldehydes and 4-hydroxycoumarin into bis(4-hydroxycoumarinyl)arylmethanes

Electrocatalytic Cascade Reaction of Aldehydes and 4-Hydroxy-6-methyl-2H-pyran-2-one

Catalyst-free tandem Knoevenagel-Michael reaction of aldehydes and pyrazolin-5-one: fast and convenient approach to medicinally relevant 4,4′-(arylmethylene)bis(1H-pyrazol-5-ol)s

Modular Access to Eight‐Membered N‐Heterocycles by Directed Carbonylative C−C Bond Activation of Aminocyclopropanes

C–C Bond Activations of Minimally Activated Cyclopropanes

Efficient non-catalytic synthesis of substituted 2,3,4,9-tetrahydro-1H-xanthen-1-ones from salicylaldehydes and dimedone

A Comparison of the Dynamics of S100B, S100A1, and S100A6 mRNA Expression in Hippocampal CA1 Area of Rats during Long-Term Potentiation and after Low-Frequency Stimulation

Electrocatalysis in MIRC reaction strategy: facile stereoselective approach to medicinally relevant spirocyclopropylbarbiturates from barbituric acids and activated olefins

Non-catalytic multicomponent rapid and efficient approach to 10-(2,4,6-trioxohexahydropyrimidin-5-yl)-3,3-dimethyl-2,3,4,9-tetrahydro-1H-xanthen-1-ones from salicylaldehydes, dimedone, and barbituric acids

Stereoselective synthesis of medicinally relevant furo[2,3-d]pyrimidine framework by thermal rearrangement of spirocyclic barbiturates

ChemInform Abstract: Branch‐Selective Alkene Hydroarylation by Cooperative Destabilization: Iridium‐Catalyzed ortho‐Alkylation of Acetanilides

ChemInform Abstract: Stereoselective Synthesis of Medicinally Relevant Furo[2,3‐d]pyrimidine Framework by Thermal Rearrangement of Spirocyclic Barbiturates

ChemInform Abstract: Non‐catalytic Multicomponent Rapid and Efficient Approach to 10‐(2,4,6‐Trioxohexahydropyrimidin‐5‐yl) ‐3,3‐dimethyl‐2,3,4,9‐tetrahydro‐1H‐xanthen‐1‐ones from Salicylaldehydes, Dimedone, and Barbituric Acids

Stereoselective synthesis of medicinally relevant furo[2,3-d]pyrimidine framework by thermal rearrangement of spirocyclic barbituratesElectronic supplementary information (ESI) available. CCDC 1423220. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5ra19169f

ChemInform Abstract: Efficient Non-Catalytic Synthesis of Substituted 2,3,4,9-Tetrahydro-1H-xanthen-1-ones from Salicylaldehydes and Dimedone

Suchergebnisse filtern