Results 11 to 20 of about 15,108 (284)

hexanes [PDF]

open access: yes, 2023
Catalytic borylations of sp3 C-H bonds occur with high selectivities for primary C-H bonds or secondary C-H bonds that are activated by nearby electron-withdrawing substituents. Catalytic borylation at tertiary C-H bonds has not been observed.
Pashenko, Alexander   +17 more
core   +1 more source

1,2-Disubstituted Bicyclo[2.1.1]hexanes as Bioisosteres of the ortho-substituted Benzene

open access: yes, 2023
1,2-Disubstitued bicyclo[2.1.1]hexanes have been designed, synthesized, and validated as a new generation of saturated bioisosteres of ortho-substituted benzenes. Incorporation of the bicyclo[2.1.1]hexane core into the structure of agrochemicals Boskalid
Iryna , Sadkova   +8 more
core   +1 more source

Bicyclo[2.1.1]hexanes by Visible Light-Driven Intramolecular Crossed [2 + 2] Photocycloadditions

open access: yes, 2022
Bicyclo[2.2.1]hexanes have become increasingly popular building blocks in medicinal chemistry as bridged scaffolds that provide unexplored chemical space.
Thorsten Bach (1397326)   +1 more
core   +2 more sources

Enantioselective photocatalytic synthesis of bicyclo[2.1.1]hexanes as orthodisubstituted benzene bioisosteres with improved biological activity

open access: yes, 2023
1,5-Disubstituted bicyclo[2.1.1]hexanes are bridged scaffolds with well-defined exit vectors that are becoming increasingly popular building blocks in medicinal chemistry since they are saturated bioisosteres of orthosubstituted phenyl rings.
Israel , Fernandez   +6 more
core   +1 more source

Development of the Lewis Acid Catalyzed Allenoate-Claisen Rearrangement. Investigations of Enantioselective Catalysis of the Allenoate-Claisen Rearrangement. Studies Towards the Total Synthesis of Erythrolide E [PDF]

open access: yes, 2004
The development of a new Lewis acid catalyzed sigmatropic reaction is described. This process, termed the allenoate-Claisen rearrangement, involves the metal-catalyzed condensation of an allenic ester with a tertiary allylic amine.
Lambert, Tristan Hayes
core   +1 more source

Chemical Profile and Biological Potential of Non-Polar Fractions from Centroceras clavulatum (C. Agardh) Montagne (Ceramiales, Rhodophyta)

open access: yesMolecules, 2011
The present study reports the Gas Chromatography-Mass Spectrometry (GC-MS) evaluation of the hexanes and dichloromethane fractions from extracts of the red alga Centroceras clavulatum (C. Agardh) Montagne. Twenty three compounds were identified, totaling
Hosana M. Debonsi   +8 more
doaj   +1 more source

Spirocyclic Acylphloroglucinol Derivatives from

open access: yesNatural Product Communications, 2014
Five spirocyclic acylphloroglucinol derivatives ( 1–5 ) have been isolated from a hexanes extract of the leaves of Hypericum pyramidatum. Pyramidatones A-D ( 1–3, 5 ) are new, and chipericumin C ( 4 ) has been previously reported. The acylphloroglucinols
Rebecca Force   +6 more
doaj   +1 more source

Dual function of active constituents from bark of Ficus racemosa L in wound healing

open access: yesBMC Complementary and Alternative Medicine, 2018
Background Different parts including the latex of Ficus racemosa L. has been used as a medicine for wound healing in the Ayurveda and in the indigenous system of medicine in Sri Lanka.
Nisansala Swarnamali Bopage   +5 more
doaj   +1 more source

Synthesis of bis-spirocyclic derivatives of 3-azabicyclo[3.1.0]hexane via cyclopropene cycloadditions to the stable azomethine ylide derived from Ruhemann's purple

open access: yesBeilstein Journal of Organic Chemistry, 2022
A reliable method for the synthesis of bis-spirocyclic derivatives of 3-azabicyclo[3.1.0]hexanes through the 1,3-dipolar cycloaddition (1,3-DC) reactions of cyclopropenes to the stable azomethine ylide – protonated form of Ruhemann's purple (PRP) has ...
Alexander S. Filatov   +4 more
doaj   +1 more source

Crystal structure of bis(3-bromomesityl)(quinolin-1-ium-8-yl)boron(III) tribromide

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2015
The title compound, C27H26.82BBr2.18N+·Br3−, is a cationic triarylborane isolated as its tribromide salt. The aryl substituents include a protonated 8-quinolyl group and two 3-bromomesityl groups.
Jungho Son   +2 more
doaj   +1 more source

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