Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Attunuri Nagireddy"'
Publikováno v:
Organic Letters. 24:5062-5067
Publikováno v:
Advanced Synthesis & Catalysis.
Publikováno v:
Organic & Biomolecular Chemistry. 20:2609-2614
We demonstrated a dual-cyclizative coupling of ynone oxime ethers with acrylamides for the synthesis of isoxazolyl 2-oxindoles. The cascade is triggered by a palladium(ii)-catalyzed ynone oxime ether cyclization, and is completed by a Heck-type coupl
Autor:
Attunuri Nagireddy, null Dattatri, Ramesh Kotipalli, Jagadeesh Babu Nanubolu, Maddi Sridhar Reddy
Publikováno v:
The Journal of Organic Chemistry. 87:1240-1248
We present here a rhodium-catalyzed oxidative three-point double annulation of enaminones with propargylic alcohols via a C-H and a C-N bond activation to access arylnaphthalene-based lignan derivatives. The key step in the reaction is the regioselec
Publikováno v:
Organic letters. 24(28)
We disclose herein a Rh(III)-catalyzed migratory three-point double annulation of
Autor:
Attunuri Nagireddy, Maddi Sridhar Reddy, Undamatla Suri Babu, Maneesh Kumar Reddy Singam, Jagadeesh Babu Nanubolu
Publikováno v:
The Journal of Organic Chemistry. 86:8069-8077
In the realm of transition-metal catalyzed arene functionalization, rhodium(III) catalysis is considered as exemplary due to its propensity to activate C-H bonds to obtain comprehensive molecular assembly. Herein, we demonstrate a new rhodium(III) ca
Publikováno v:
The Journal of Organic Chemistry. 85:6970-6980
A regio- and stereoselective synthesis of unsymmetrically substituted pentafulvenes is reported via the condensation of readily available ynones and amino crotonates under very mild conditions. The mechanism of this 3 + 2 annulation involved a vinylo
Autor:
Manda Rajesh, Attunuri Nagireddy, Maddi Sridhar Reddy, Veeramalla Ganesh, Maneesh Kumar Reddy Singam
Publikováno v:
Organic Chemistry Frontiers. 7:30-34
A regioselective carbonickelation followed by cyclization, an arylative cyclization, of ortho functional diaryl acetylenes is achieved apparently through an electrophile driven alkyne polarization. A series of selectively substituted di aryl isoquino
Publikováno v:
Green Chemistry. 22:2370-2374
Here, we have demonstrated a strategic rapid approach for the synthesis of benzonitriles and cyanofluorenes via the [3 + 3] benzannulation of readily available alkynones and α-cyanocrotonates, a protocol par excellence for aryl nitriles. This decarb
Publikováno v:
Organicbiomolecular chemistry. 20(13)
Metal-catalyzed cyclizative cross-coupling reactions have attracted enormous attention due to their unique cascade nature. We demonstrated, herein, a dual-cyclizative coupling of ynone oxime ethers with acrylamides for the synthesis of methylene-link