Rhodium-catalyzed tandem C–H activation and aza-Michael addition of 2-arylquinazolin-4-ones with acrylates for the synthesis of pyrrolo[2,1-b]quinazolin-9(1H)-one derivatives
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Jian-jun Yuan | Qin Yang | Z. Deng | Yiyuan Peng | Xin Jiang | Chuyi Yu | Xuechun Mao
[1] J. Wang,et al. Rhodium(I)-Catalyzed Sequential C(sp)-C(sp(3)) and C(sp(3))-C(sp(3)) Bond Formation through Migratory Carbene Insertion. , 2015, Angewandte Chemie.
[2] T. Loh,et al. Rhodium-catalysed C(sp2)–C(sp2) bond formation via C–H/C–F activation , 2015, Nature Communications.
[3] Yong-sheng Zheng,et al. Ruthenium-catalyzed oxidative coupling of 2-aryl-4-quinazolinones with olefins: synthesis of pyrrolo[2,1-b]quinazolin-9(1H)-one motifs. , 2015, Organic & biomolecular chemistry.
[4] Wanzhi Chen,et al. Efficient Approach to Mesoionic Triazolo[5,1-a]isoquinolium through Rhodium-Catalyzed Annulation of Triazoles and Internal Alkynes. , 2015, Organic letters.
[5] Xiao‐Feng Wu,et al. Palladium-catalyzed dicarbonylative synthesis of tetracycle quinazolinones. , 2015, Organic & biomolecular chemistry.
[6] Z. Deng,et al. Rhodium-Catalyzed Regioselective Direct C–H Amidation of 2,4-Diarylquinazoline with Sulfonyl Azides: An Example of Steric Hindrance Regulated Mono- and Diamidation Selectivity , 2015 .
[7] Jillian E. Spangler,et al. Synthesis of Complex Hexacyclic Compounds via a Tandem Rh(II)-Catalyzed Double-Cyclopropanation/Cope Rearrangement/Diels–Alder Reaction , 2014, Organic letters.
[8] Jian-jun Yuan,et al. Synthesis of 4-alkynylquinazolines: Pd-Cu-cocatalyzed coupling of quinazoline-4-tosylates with terminal alkynes using N-heterocyclic carbenes as ligands. , 2014, Organic & biomolecular chemistry.
[9] P. Parvatkar,et al. Intramolecular Diels–Alder reaction as a key step in tandem or sequential processes: a versatile tool for the synthesis of fused and bridged bicyclic or polycyclic compounds , 2014 .
[10] M. Shibuya,et al. Tandem ruthenium-catalyzed transfer-hydrogenative cyclization/intramolecular Diels-Alder reaction of enediynes affording dihydrocoumarin-fused polycycles. , 2014, Organic letters.
[11] Qin Yang,et al. Cross-coupling/annulations of quinazolones with alkynes for access to fused polycyclic heteroarenes under mild conditions. , 2014, Organic & biomolecular chemistry.
[12] Qin Yang,et al. Palladium-Catalyzed Cyanation of Quinazoline-4-tosylates for Access to 4-CN-Functionalized Quinazolines , 2013 .
[13] Qin Yang,et al. Synthesis of 4-Arylquinazolines by Arylation of Quinazolin-4-ones under Mild Conditions , 2013 .
[14] Fen Wang,et al. C-C, C-O and C-N bond formation via rhodium(III)-catalyzed oxidative C-H activation. , 2012, Chemical Society reviews.
[15] Jaulang Hwang,et al. One-pot synthesis of luotonin A and its analogues. , 2011, Organic letters.
[16] V. Pike,et al. A convenient one-pot procedure for the synthesis of 2-aryl quinazolines using active MnO2 as oxidant , 2010 .
[17] Y. Chu,et al. Total synthesis of asperlicin C, circumdatin F, demethylbenzomalvin A, demethoxycircumdatin H, sclerotigenin, and other fused quinazolinones. , 2010, Organic & biomolecular chemistry.
[18] F. Liu,et al. Palladium-catalyzed sequential cyanation/n-addition/N-arylation in one-pot: efficient synthesis of luotonin A and its derivatives. , 2009, Organic letters.
[19] Yu W. Chu,et al. Tin triflate-mediated total synthesis of circumdatin F, sclerotigenin, asperlicin C, and other quinazolino[3,2-a][1,4]benzodiazepines. , 2009, Chemical communications.
[20] Y. Chu,et al. Zinc triflate-catalyzed synthesis of pyrazino[2,1-b]quinazoline-3,6-diones , 2008 .
[21] M. Malacria,et al. Radical cyclization of N-acylcyanamides: total synthesis of luotonin A. , 2007, Angewandte Chemie.
[22] N. Argade,et al. The Chemistry of Recently Isolated Naturally Occurring Quinazolinone Alkaloids , 2006 .
[23] P. Guiry,et al. Synthesis of Quinazolinones and Quinazolines , 2005 .
[24] J. Bergman,et al. Recent Developments in the Field of Quinazoline Chemistry , 2003 .
[25] J. Michael. Quinoline, quinazoline and acridone alkaloids (July 1999 to June 2000) , 2001 .
[26] J. Michael. Quinoline, quinazoline and acridone alkaloids. , 2001, Natural product reports.
[27] Rahbaek,et al. Circumdatins D, E, and F: further fungal benzodiazepine analogues from aspergillus ochraceus , 1999, Journal of natural products.
[28] J. Frisvad,et al. Circumdatin A, B, and C: Three New Benzodiazepine Alkaloids Isolated from a Culture of the Fungus Aspergillus ochraceus. , 1999, The Journal of organic chemistry.
[29] T. Nomura,et al. TWO NEW PYRROLOQUINAZOLINOQUINOLINE ALKALOIDS FROM PEGANUM NIGELLASTRUM , 1997 .
[30] S. Meegalla,et al. Synthesis and pharmacological evaluation of isoindolo[1,2-b]quinazolinone and isoindolo[2,1-a]benzimidazole derivatives related to the antitumor agent batracylin. , 1994, Journal of medicinal chemistry.
[31] B. E. Evans,et al. Design of nonpeptidal ligands for a peptide receptor: cholecystokinin antagonists. , 1987, Journal of medicinal chemistry.
[32] B. E. Evans,et al. Cholecystokinin antagonists. Synthesis of asperlicin analogues with improved potency and water solubility. , 1986, Journal of medicinal chemistry.
[33] J M Liesch,et al. Asperlicin, a novel non-peptidal cholecystokinin antagonist from Aspergillus alliaceus. Structure elucidation. , 1985, The Journal of antibiotics.
[34] R. Chang,et al. Asperlicin, a novel non-peptidal cholecystokinin antagonist from Aspergillus alliaceus. Fermentation, isolation and biological properties. , 1985, The Journal of antibiotics.
[35] J M Liesch,et al. A potent nonpeptide cholecystokinin antagonist selective for peripheral tissues isolated from Aspergillus alliaceus. , 1985, Science.