Results 141 to 150 of about 1,568 (180)
Some of the next articles are maybe not open access.

Electropolymerization of fused pyrroles as new heteroaromatic polymers

Synthetic Metals, 1989
Abstract The electro-oxidative polymerization of fused pyrroles+, i.e., DMPP[3,2-b] and PP[2,3-b] in acetonitrile solutions led to the formation of brown-black, polymeric films+ (poly-DMPP[3,2-b] and poly-PP[2,3-b]) on the electrode surfaces. Both films showed reversible, well-defined oxidation-reduction responses in both acetonitrile and aqueous ...
N.Oyama   +7 more
openaire   +1 more source

A General Synthesis of Pyrroles and Fused Pyrrole Systems from Ketones and Amino Acids

The Journal of Organic Chemistry, 1996
The lithium enolates of ketones react with BOC-α-amino aldehydes and BOC-α-amino ketones to afford aldol intermediates that cyclize under acidic conditions to yield pyrroles. The BOC-amino aldehydes and ketones are readily available from α-amino acids.
Pamela Nagafuji, Mark Cushman
openaire   +1 more source

A new synthesis of pyrroles fused with polycyclic skeletons

Journal of the Chemical Society, Perkin Transactions 1, 1997
The Diels–Alder reaction of β-sulfonylnitroethylene with cyclopentadiene, cyclohexadiene or substituted anthracenes followed by treatment with ethyl isocyanoacetate in the presence of DBU gives pyrroles fused with bicyclo[2.2.1]heptadiene and bicyclo[2.2.2]octadiene skeletons, or triptycene-types of pyrrole, respectively, which are precursors for novel
Satoshi Ito   +2 more
openaire   +1 more source

Expeditious Synthesis of Imidazole‐ and Pyrrole‐Fused Benzodiazocines

European Journal of Organic Chemistry, 2010
AbstractA straightforward strategy for the synthesis of imidazole‐fused benzodiazocine from 1‐(2‐nitrophenyl)‐1H‐imidazole‐2‐carbaldehyde via Morita–Baylis–Hillman reaction followed by reductive intramolecular cyclization is described. Alternatively the Horner–Wadsworth–Emmons reaction of this substrate with triethyl phosphonoacetate yielded (E)‐ethyl ...
Amita Mishra, Sanjay Batra
openaire   +1 more source

Fused Thiophene‐Pyrrole‐Containing Ring Systems up to a Heterodecacene

Angewandte Chemie International Edition, 2015
AbstractA new class of π‐conjugated polycyclic hydrocarbons that promises interesting electronic properties is presented. The synthesis and extension of the S,N‐heteroacene series consisting of only five‐membered heterocyclic rings up to a very long, stable, and still soluble decacene SN10 is realized by multiple Pd‐catalyzed aminations of halogenated ...
Christoph, Wetzel   +5 more
openaire   +2 more sources

Regioselective synthesis of pentathiepines fused with pyrrole, thiophene, or indole rings

Russian Chemical Bulletin, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
L. S. Konstantinova   +2 more
openaire   +1 more source

An approach to the synthesis of novel pyrrole fused heterocycles

2020
Pirol ve pirol türevleri doğada sıkça bulunmaları ve gösterdikleri biyolojik aktiviteler nedeni ile organik sentezin önemli yapı bloklarıdır. Yapısında pirol içeren heterosiklik bileşiklerin elektrofilik halkalaşma reaksiyonları ile sentezi literatürde yer alan önemli ve etkili proseslerdendir. Bu çalışmada, N-alkinil-2-fenil-sübstütiye pirol türevleri
openaire   +2 more sources

Pyrroles and Fused Pyrroles: Synthesis and Therapeutic Activities

Mini-Reviews in Organic Chemistry, 2013
Mosaad Mohamed, Samar Fathallah
openaire   +1 more source

Pyrrole-Sharing Fused Hybrids of Porphyrins and N-Confused Azaporphyrins

Organic Letters
meso-(α-Amino)tripyrrin-substituted NiII porphyrin, which was prepared by the substitution reaction of meso-ZnII-(α-chloro)tripyrrin-substituted NiII porphyrin with ammonia and subsequent demetalation, served as a key intermediate to provide pyrrole-sharing fused hybrids of NiII porphyrin and PdII N-confused (NC) azaporphyrin and NiII porphyrin and NC ...
Li Liu   +9 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy