GAP chemistry for pyrrolyl coumarin derivatives: a highly efficient one-pot synthesis under catalyst-free conditions
出版年份 2013 全文链接
标题
GAP chemistry for pyrrolyl coumarin derivatives: a highly efficient one-pot synthesis under catalyst-free conditions
作者
关键词
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出版物
GREEN CHEMISTRY
Volume 15, Issue 12, Pages 3307
出版商
Royal Society of Chemistry (RSC)
发表日期
2013-09-25
DOI
10.1039/c3gc41799a
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- (2013) Xian Feng et al. ORGANIC LETTERS
- Efficient Synthesis of Functionalized Dihydro-1H-indol-4(5H)-ones via One-Pot Three-Component Reaction under Catalyst-Free Conditions
- (2013) Hui-Yan Wang et al. ACS Combinatorial Science
- Influence of Chlorine or Fluorine Substitution on the Estrogenic Properties of 1-Alkyl-2,3,5-tris(4-hydroxyphenyl)-1H-pyrroles
- (2012) Anja Schäfer et al. JOURNAL OF MEDICINAL CHEMISTRY
- Molybdate sulfuric acid as a reusable solid catalyst in the synthesis of 2,3,4,5-tetrasubstituted pyrroles via a new one-pot [2+2+1] strategy
- (2012) Fatemeh Tamaddon et al. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
- Modulating the Reactivity of Functionalized N,S-Ketene Acetal in MCR: Selective Synthesis of Tetrahydropyridines and Thiochromeno[2,3-b]pyridines via DABCO-Catalyzed Tandem Annulation
- (2012) Li-Rong Wen et al. JOURNAL OF ORGANIC CHEMISTRY
- Palladium-Catalyzed Cascade Process To Construct 1,2,5-Trisubstituted Pyrroles
- (2012) Yong-Qiang Zhang et al. JOURNAL OF ORGANIC CHEMISTRY
- Silica-supported bismuth(III) chloride as a new recyclable heterogeneous catalyst for the Paal–Knorr pyrrole synthesis
- (2012) Kioumars Aghapoor et al. JOURNAL OF ORGANOMETALLIC CHEMISTRY
- Efficient Domino Approaches to Multifunctionalized Fused Pyrroles and Dibenzo[b,e][1,4]diazepin-1-ones
- (2012) Bo Jiang et al. ORGANIC LETTERS
- Facile Synthesis of Dispirooxindole-Fused Heterocycles via Domino 1,4-Dipolar Addition and Diels–Alder Reaction of in Situ Generated Huisgen 1,4-Dipoles
- (2012) Jing Sun et al. ORGANIC LETTERS
- An Efficient Synthesis of Pyrrolo[2,3,4-kl]acridin-1-one Derivatives Catalyzed by l-Proline
- (2012) Huiyuan Wang et al. ORGANIC LETTERS
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- (2012) Ming Li et al. ORGANIC LETTERS
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- (2012) Vanampally Chandrashaker et al. TETRAHEDRON
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- (2012) Ying Han et al. TETRAHEDRON
- An efficient one-pot organocatalytic synthesis of 9-(1H-indol-3-yl)-xanthen-4-(9H)-ones under mild aqueous micellar conditions
- (2012) Nemai C. Ganguly et al. TETRAHEDRON LETTERS
- A multi-component domino reaction for the direct access to polyfunctionalized indolesvia intermolecular allylic esterification and indolation
- (2011) Bo Jiang et al. CHEMICAL COMMUNICATIONS
- A grinding-induced catalyst- and solvent-free synthesis of highly functionalized 1,4-dihydropyridines via a domino multicomponent reaction
- (2011) Atul Kumar et al. GREEN CHEMISTRY
- The GAP chemistry for chiral N-phosphonyl imine-based Strecker reaction
- (2011) Parminder Kaur et al. GREEN CHEMISTRY
- Three-Component Synthesis of Polysubstituted Pyrroles from α-Diazoketones, Nitroalkenes, and Amines
- (2011) Deng Hong et al. ORGANIC LETTERS
- Enone–Alkyne Reductive Coupling: A Versatile Entry to Substituted Pyrroles
- (2011) Benjamin B. Thompson et al. ORGANIC LETTERS
- Silver-Catalyzed Intramolecular Chloroamination of Allenes: Easy Access to Functionalized 3-Pyrroline and Pyrrole Derivatives
- (2011) Masahiro Sai et al. ORGANIC LETTERS
- Electronically Intercommunicating Iron Centers in Di- and Tetraferrocenyl Pyrroles§
- (2011) Alexander Hildebrandt et al. ORGANOMETALLICS
- Efficient one-pot synthesis of spiro[indoline-3,4′-pyrazolo[3,4-e][1,4]thiazepine]dione via three-component reaction
- (2011) Hui Chen et al. TETRAHEDRON
- An efficient one-pot synthesis of tetra-substituted pyrroles
- (2011) Elmira Ghabraie et al. TETRAHEDRON
- A facile and efficient ultrasound-assisted synthesis of novel dispiroheterocycles through 1,3-dipolar cycloaddition reactions
- (2011) Yu Hu et al. ULTRASONICS SONOCHEMISTRY
- Rapid and Efficient Ultrasound-Assisted Method for the Combinatorial Synthesis of Spiro[indoline-3,4′-pyrano[2,3-c]pyrazole] Derivatives
- (2011) Yi Zou et al. ACS Combinatorial Science
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- (2010) Parminder Kaur et al. CHEMICAL COMMUNICATIONS
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- (2010) Hui Chen et al. JOURNAL OF COMBINATORIAL CHEMISTRY
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- (2010) Chunling Shi et al. JOURNAL OF COMBINATORIAL CHEMISTRY
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- (2010) Yuling Li et al. JOURNAL OF COMBINATORIAL CHEMISTRY
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- (2010) Daniel J. St-Cyr et al. JOURNAL OF ORGANIC CHEMISTRY
- Asymmetric CatalyticN-Phosphonyl Imine Chemistry: The Use of Primary Free Amino Acids and Et2AlCN for Asymmetric Catalytic Strecker Reaction
- (2010) Parminder Kaur et al. JOURNAL OF ORGANIC CHEMISTRY
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- (2010) Sukhendu Maiti et al. JOURNAL OF ORGANIC CHEMISTRY
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- (2010) Qingjiang Li et al. ORGANIC LETTERS
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- (2010) Fernanda M. Ribeiro Laia et al. TETRAHEDRON
- Short and efficient synthesis of 2H-pyrroles from 7-oxanorbornadiene derivatives
- (2010) Adrien Soret et al. TETRAHEDRON
- Efficient One-Pot Three-Component Synthesis of Fused Pyridine Derivatives in Ionic Liquid
- (2010) Zhibin Huang et al. ACS Combinatorial Science
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- (2009) Georgia Melagraki et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
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- (2009) Xiangwei Du et al. JOURNAL OF ORGANIC CHEMISTRY
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- (2009) Barry M. Trost et al. ORGANIC LETTERS
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- (2009) Prakasam Thirumurugan et al. TETRAHEDRON LETTERS
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- (2007) Shunsuke Chiba et al. ORGANIC LETTERS
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