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Enantioselective synthesis of C3-functionalized 2,1-benzothiazine 2,2-dioxides by N-heterocyclic carbene catalysis

Chemical Communications
The direct and highly enantioselective C3-functionalization of the 2,1-benzothiazine 2,2-dioxide skeleton using NHC-catalyzed generation of chiral α,β-unsaturated acylazoliums, showcasing a synthesis pathway with enhanced pharmacological potential.
Karina Mroczyńska   +2 more
openaire   +2 more sources

Regioselective synthesis of pyrimido[5,4‐c][2,1]benzothiazines by reactions of β‐chloroaldehydes with n‐c‐n binucleophiles

Journal of Heterocyclic Chemistry, 2009
Abstract magnified imageThe method of pyrimidine ring fusion at the [c] side of benzothiazines based on the reaction of their chloroaldehyde derivatives with amidines is described. Formation of the structural isomers of reaction products was investigated, and regioselectivity of heterocyclization reactions was shown.
Kirill Popov   +3 more
openaire   +1 more source

Searching for innovative quinolone-like scaffolds: synthesis and biological evaluation of 2,1-benzothiazine 2,2-dioxide derivatives

MedChemComm, 2012
Quinolones are a widely used class of antibacterial agents characterized by overall favourable pharmacokinetic and pharmacodynamic characteristics. Unfortunately, both nosocomial and community acquired resistances to these agents are increasing. Thorough structure–activity relationship (SAR) studies have demonstrated that even drastic manipulation of ...
PIERONI, MARCO   +5 more
openaire   +3 more sources

Studies of 2,1-benzothiazine, silver-catalyzed rearrangement and 1,5-hydride shift

2018
Title from PDF of title page (University of Missouri--Columbia, viewed on Feb 26, 2010). ; The entire thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file; a non-technical public abstract appears in the public.pdf file. ; Thesis advisor: Dr. Michael Harmata. ; Vita. ; Ph.D.
openaire   +2 more sources

Facile Preparation of 3,4-Dihydro-2,1-benzothiazine 2,2-Dioxides and Related Reaction with 1,3-Diiodo-5,5-dimethylhydantoin under Photochemical Conditions

Synlett, 2009
3,4-Dihydro-2,1-benzothiazine 2,2-dioxides were easily obtained in good yields by the reaction of N-methyl 2-arylethane-sulfonamides with 1,3-diiodo-5,5-dimethylhydantoin (D1H) under irradiation with a tungsten lamp. When N-benzyl 2-phenylethane-sulfonamide was treated with DIH under the same conditions, the corresponding N-benzyl 3,4-dihydro-2,1 ...
Hideo Togo   +2 more
openaire   +1 more source

ChemInform Abstract: Preparation of 3,4‐Dihydro‐2,1‐benzothiazine 2,2‐Dioxide Skeleton from N‐Methyl 2‐(Aryl)ethanesulfonamides with (Diacetoxyiodo)arenes.

ChemInform, 2000
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Hideo Togo   +2 more
openaire   +1 more source

ChemInform Abstract: HERST. EINIGER 4‐HYDROXYL‐1‐METHYL‐1H‐2,1‐BENZOTHIAZIN‐3‐CARBOXANILID‐2,2‐DIOXIDE

Chemischer Informationsdienst, 1972
AbstractSulfoessigsäure (Ia) liefert über Ester (Ib) und das Sulfonsäurechlorid (IIa) das Anilid (IIb), das nach Hydrolyse zur freien Säure (III) durch Polyphosphorsäure zu (IV) cyclisiert werden kann.
openaire   +1 more source

In-silico modeling and in-vitro studies of 2,1-benzothiazine-2,2-dioxide based hydrazone derivatives as α-glucosidase inhibitors.

Pakistan journal of pharmaceutical sciences, 2022
Diabetes mellitus (DM) is a metabolic disorder characterized by frequent urination, hunger and high blood sugar level. α-glucosidase inhibitors are considered as a frontline treatment for the DM. This research article deals with the identification of benzothiazine derivatives as α-glucosidase inhibitors through in-silico techniques and then the ...
Shakeel, Ahmad   +6 more
openaire   +1 more source

Preparation of some 4‐hydroxyl‐1‐methyl‐1H‐2,1‐benzothiazine‐3‐carboxanilide 2,2‐dioxides

Journal of Heterocyclic Chemistry, 1972
AbstractAn improved, 3‐step synthesis of 3,4‐dihydro‐1‐methyl‐1H‐2,1‐benzothiazin‐4‐one 2,2‐dioxide has been developed. This general method offers a more facile entrance into the 2,1‐benzothiazine 2,2‐dioxide heterocyclic system than was heretofore available.
openaire   +1 more source

Dilithiation of a 2,1-Benzothiazine

HETEROCYCLES, 2016
Michael Harmata, Nathan L. Calkins
openaire   +1 more source

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