欢迎您！东篱公司
退出
-
申报数据库
-
立项数据库
-
成果数据库
-
项目获奖数据库
同期刊论文项目
同项目期刊论文
A Cascade Coupling Strategy for One-Pot Total Synthesis of b-Carboline and Isoquinoline-Containing N
Iodine-promoted selective synthesis of substituted aminothiazole via a self-sorting reaction network
Auto-tandem catalysis: synthesis of 4H-pyrido[1,2-a]- pyrimidin-4-ones via copper-catalyzed aza-Mich
A sustainable byproduct catalyzed domino strategy: facile synthesis of a-formyloxy and acetoxy keton
Unsymmetrical N and/or O-bridged calixarene derivatives: synthesis, structure and encapsulation of s
Convergent integration of two self-labor domino sequences: a novel method for the synthesis of oxazo
Iodine-Promoted Sequential C(sp(3))-H Functionalization Reactions: An Annulation Strategy for the Co
Target-oriented synthesis: miscellaneous synthetic routes to access 1,4-enediones through the coupli
An integration of condensation/Ullmann-type coupling/bicyclization sequences: copper-catalyzed three
Synthesis of Tetrasubstituted Unsymmetrical 1,4-Enediones via Copper-Promoted Autotandem Catalysis a
Convergent integration of three self-sorting domino sequences: three-component direct synthesis of 3
Iodine-promoted efficient synthesis of diheteroaryl thioethers via the integration of iodination/con
One-pot synthesis of polyfunctional pyrazoles: an easy access to α-diazoketones from arylglyoxal mon
I2 promoted domino oxidative cyclization for one-pot synthesis of 2-acylbenzothiazoles via metal-fre
Metal-free dual sp3 C-H functionalization: I2-promoted domino oxidative cyclization to construct 2,5
A facile synthesis of indole-furan conjugates via integration of convergent and linear domino reacti
Metal-Free sp3 C-H Bond Dual-(Het)arylation: I2-Promoted Domino Process to Construct 2,2-Bisindolyl-
A Novel and Highly Regioselective Route to Construct Methylthio-Substituted Pyridazines from Aryl Me
Direct Synthesis of Substituted Naphthalenes from 1,3-Dicarbonyl Compounds and 1,2-Bis(halomethyl)be
Unexpected synthesis of indolo[1,2-c] quinazolines by a sequential Ugi 4CC–Staudinger–aza-Wittig–nuc
Temperature-Dependent Regioselective Synthesis of 1,2,4-Triazino[2,3-b]indazoles and 3H-1,4-Benzodia
Povarov-Type Reaction Using Methyl as New Input: Direct Synthesis of Substituted Quinolines by I-2-M
Synthesis of trisubstituted isoxazoles via in situ trapping strategy from a-nitro carbonyl compounds
An Efficient Synthesis of Novel Fused Cycloheptatrienes through Mn(II)-Mediated Formal Intermolecula
I2-promoted direct one-pot synthesis of 2-aryl-3-(pyridine-2-ylamino) imidazo[1,2-a]pyridines from a
Design and Synthesis of 2？Acylbenzothiazoles via In Situ Cross- Trapping Strategy from Benzothiazole
New ef？cient synthesis of 2,3,4-trisubstituted 3,4-dihydroquinazolines by a Ugi 4CC/Staudinger/aza-W
New efficient synthesis of trisubstituted imidazolidine-2-thiones and thiazoles via vinyliminophosph
Unexpected C？C Bond Cleavage: A Route to 3,6-Diarylpyridazines and 6-Arylpyridazin-3-ones from 1,3-D
Efficient one-pot synthesis of 1H-pyrazolo[1,5-b]indazoles by a domino staudinger-aza-wittig cycliza
Highly selective colorimetric sensing pyrophosphate in water by a NBD-phenoxo-bridged dinuclear Zn(I
Synthesis of 1,2,4,5-Tetrasubstituted Imidazoles by a Sequential Aza- Wittig/Michael/Isomerization R
I2？Promoted Selective Oxidative Cross-Coupling/Annulation of 2？Naphthols with Methyl Ketones: A Stra
Copper-Catalyzed Domino Synthesis of 2-Imino-1H-imidazol-5(2H)-ones and Quinoxalines Involving C-C B
Synthesis of trisubstituted imidazoles via a convergent reaction network from methyl ketones and ben
One-pot total synthesis: the first total synthesis of chiral alkaloid pimprinol A and the facile con
Synthesis of substituted naphthalenes from alpha-substituted ketones and 1,2-bis(halomethyl)benzenes
Logical design and synthesis of indole-2,3-diones and 2-hydroxy-3(2H)-benzofuranones via one-pot int
Metal-free dual sp3 CeH functionalization: I2-promoted domino oxidative cyclization to construct 2,5
I2-promoted direct one-pot synthesis of 2,2-bisindolyl-1- arylethanones from multiform substrates ar
A new route to construct 1,2-dihydroquinoxaline and 1,4-benzoxazine derivatives stereoselectively an
位置：