Results 81 to 90 of about 17,027 (206)

Electrophilic Substitutions of Indoles and Pyrroles: [PDF]

open access: yes, 2007
The kinetics of the electrophilic substitutions of indoles and pyrroles have been investigated and new sythetic applications (i.e. electrophilic allylations and benzylations of indoles and regio- and stereoselective ring opening reactions of epoxides ...
Westermaier, Martin
core  

Controlled Oxidation of Pyrroles: Synthesis of Highly Functionalized γ‑Lactams [PDF]

open access: yes, 2016
The oxidation of pyrroles usually leads to uncontrolled polymerization and decomposition. To overcome this problem, the controlled oxidation of substituted pyrroles with Dess-Martin periodinane is reported.
James K. Howard (1973647)   +3 more
core   +1 more source

Preparation and functionalization of regioselectively substituted pyrroles/ [PDF]

open access: yes, 1993
The reaction of 1-substituted vinamidinium salts with sarcosine ethyl ester produced 2,3-disubstituted pyrroles; a similar reaction with glycine ethyl ester gave 2,5-disubstituted pyrroles.
Smith, Lana L.
core  

Lewis acid-catalyzed synthesis of functionalized pyrroles [PDF]

open access: yes, 2009
The synthesis of highly functionalized pyrroles is described. The sequence involves the preliminary preparation of alpha-aminohydrazones by Michael addition of primary amines to 1,2-diaza-1,3-butadienes.
GIORGI G   +13 more
core   +1 more source

The intricacies of the stacking interaction in a pyrrole–pyrrole system [PDF]

open access: yesStructural Chemistry, 2016
Extensive calculations of potential energy surfaces for parallel-displaced configurations of pyrrole–pyrrole systems have been carried out by the use of a dispersion-corrected density functional. System geometries associated with the energy minima have been found. The minimum interaction energy has been calculated as −5.38 kcal/mol.
openaire   +1 more source

Catalytic Asymmetric Hydrogenation of 2,3,5-Trisubstituted Pyrroles [PDF]

open access: yes, 2016
Catalytic asymmetric hydrogenation of N-Boc-protected pyrroles proceeded with high enantioselectivity by using a ruthenium catalyst modified with a trans-chelating chiral bisphosphine PhTRAP.
Masato Ohsumi (2458024)   +3 more
core   +1 more source

Efficient Synthesis of Highly Functionalised 5-oxo-4,5-Dihydro-1H-Pyrroles and 5-Oxo-2,5-Dihydro-1H-Pyrroles Derivatives [PDF]

open access: yes, 2010
Methyl 2-(2-benzoylphenylamino)-2-oxoacetate and dimethyl 2,2′-(4,4′-methylenebis(4,1- phenylene)bis(azanediyl)) bis(2-oxoacetate) undergo a smooth reaction with triphenylphosphine and dialkyl acetylenedicarboxylates to produce corresponding highly ...
Ali Reza Dadrass   +2 more
core   +1 more source

New synthetic strategies towards indolizines and pyrroles [PDF]

open access: yes, 2015
Indolizines and pyrroles are considered as “privileged” structures since their skeletons were found in many biologically active natural products and they possess a wide range of pharmaceutical properties.
Kücükdisli, Murat
core   +4 more sources

Gold(I)-Catalyzed Intra- and Intermolecular Alkenylations of β‑Yne-pyrroles: Facile Formation of Fused Cycloheptapyrroles and Functionalized Pyrroles [PDF]

open access: yes, 2016
An efficient gold­(I)-catalyzed alkenylation of β-alkyne-substituted pyrroles is reported. The intramolecular reaction gives straightforward access to different types of seven-membered-ring-fused pyrroles with endo-selectivity, and the intermolecular ...
Bin Pan (742525)   +5 more
core   +1 more source

Regioselective modification of pyrroles : applications towards lamellarins & pyrrolidine analogues [PDF]

open access: yes, 2010
In the past few decades, an extensive family of structurally intriguing and biologically active pyrrolic natural products were recognised. Many of these compounds were isolated from marine organisms and show potent biological activity, and as such have ...
Ng, SMY (15928025)
core   +1 more source

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