Results 31 to 40 of about 2,874,801 (150)

ELECTROPHILIC CYCLIZATION OF DITERPENOIDS [PDF]

open access: yesChemistry Journal of Moldova: General, Industrial and Ecological Chemistry, 2006
A review of diterpenoid cyclization initiated by electrophilic reagents is provided. Conventional protonic and Lewis acids are examined along with superacids as initiators of cyclization cascade.
Veaceslav Kulciţki   +3 more
doaj  

Nickel-catalyzed switchable arylative/endo-cyclization of 1,6-enynes

open access: yesNature Communications
Carbo- and heterocycles are frequently used as crucial scaffolds in natural products, fine chemicals, and biologically and pharmaceutically active compounds.
Wenfeng Liu   +4 more
doaj   +1 more source

Oxidative radical ring-opening/cyclization of cyclopropane derivatives

open access: yesBeilstein Journal of Organic Chemistry, 2019
The ring-opening/cyclization of cyclopropane derivatives has drawn great attention in the past several decades. In this review, recent efforts in the development of oxidative radical ring-opening/cyclization of cyclopropane derivatives, including ...
Yu Liu   +7 more
doaj   +1 more source

A strategy for sequence control in vinyl polymers via iterative controlled radical cyclization

open access: yesNature Communications, 2016
There is a growing interest in sequence-controlled polymers toward advanced functional materials. However, control of side-chain order for vinyl polymers has been lacking feasibility in the field of polymer synthesis because of the inherent feature of ...
Yusuke Hibi, M. Ouchi, M. Sawamoto
semanticscholar   +1 more source

Synthesis and Transformations of di-endo-3-Aminobicyclo-[2.2.2]oct-5-ene-2-carboxylic Acid Derivatives

open access: yesMolecules, 2011
all-endo-3-amino-5-hydroxybicyclo[2.2.2]octane-2-carboxylic acid (13) and all-endo-5-amino-6-(hydroxymethyl)bicyclo[2.2.2]octan-2-ol (10) were prepared via dihydro-1,3-oxazine or g-lactone intermediates by the stereoselective functionalization of an N ...
Márta Palkó   +2 more
doaj   +1 more source

Nickel-catalyzed electrophiles-controlled enantioselective reductive arylative cyclization and enantiospecific reductive alkylative cyclization of 1,6-enynes

open access: yesNature Communications
Transition metal-catalyzed asymmetric cyclization of 1,6-enynes is a powerful tool for the construction of chiral nitrogen-containing heterocycles.
Wenfeng Liu   +4 more
doaj   +1 more source

Metal-Free Synthesis of N-Heterocycles via Intramolecular Electrochemical C-H Aminations

open access: yesFrontiers in Chemistry, 2022
N-heterocycles are key structural units in many drugs, biologically interesting molecules and functional materials. To avoid the residues of metal catalysts, the construction of N-heterocycles under metal-free conditions has attracted much research ...
Huiqiao Wang   +4 more
doaj   +1 more source

Efficient backbone cyclization of linear peptides by a recombinant asparaginyl endopeptidase

open access: yesNature Communications, 2015
Cyclotides are diverse plant backbone cyclized peptides that have attracted interest as pharmaceutical scaffolds, but fundamentals of their biosynthetic origin remain elusive.
K. Harris   +10 more
semanticscholar   +1 more source

Straightforward synthesis of pyrimido[4,5-e][1,4]diazepines via 6-aminopyrimidin-5-carbaldehydes

open access: yesArabian Journal of Chemistry, 2019
A high-throughput method to obtain several pyrimido[4,5-e][1,4]diazepines is described by a two-step acylation/cyclization sequence from key intermediates 6-amino-5-(amino)methylpyrimidines, which were prepared from the precursor 6-aminopyrimidin-5 ...
Jose M. de la Torre   +2 more
doaj  

SpyTag/SpyCatcher Cyclization Enhances the Thermostability of Firefly Luciferase

open access: yesPLoS ONE, 2016
SpyTag can spontaneously form a covalent isopeptide bond with its protein partner SpyCatcher. Firefly luciferase from Photinus pyralis was cyclized in vivo by fusing SpyCatcher at the N terminus and SpyTag at the C terminus.
M. Si, Qing-tao Xu, Ling Jiang, He Huang
semanticscholar   +1 more source

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