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A new visible-light-promoted oxidative coupling of vinylarenes with cyclic ethers has been developed using rose bengal as photocatalyst and tert-butyl hydrogenperoxide(TBHP) as oxidant under ambient air at room temperature. A library of α-oxyalkylated ketones with broad functionalities has been synthesized in moderate to good yields. A radical mechanism is suggested for the present protocol. 相似文献
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An alanine-derived aminohydroxyphosphine ligand was developed for copper-catalyzed asymmetric conjugate addition of organozinc reagents to alpha,beta-unsaturated carbonyl compounds. This new tridentate ligand induces consistently high enantioselectivity in reactions of a variety of acyclic substrates. Theoretical mechanistic analysis suggests that the C-C bond formation takes place through a highly ordered transition state by the coordination of the phosphorus and nitrogen atoms to the copper(III) and zinc(II) atoms, respectively, and of the oxygen anion to both the metal centers. 相似文献
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Sharmistha Urinda Dhiman Kundu Adinath Majee Alakananda Hajra 《Heteroatom Chemistry》2009,20(4):232-234
A mild, efficient, and environment friendly method has been developed for the synthesis of 14‐alkyl or aryl‐14H‐dibenzo[a, j]xanthenes by condensation of 2‐naphthol and aldehydes in the presence of a catalytic amount of indium(III) triflate (2 mol%) in water at 100°C. Different types of aromatic and aliphatic aldehydes are used in the reaction, and in all cases the products synthesized in moderate to excellent yields. © 2009 Wiley Periodicals, Inc. Heteroatom Chem 20:232–234, 2009; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20539 相似文献
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Over the years, various strategies have been reported for the synthesis of imidazo[1,2‐a]pyridines due to their importance in different fields. In this account, we represent the methods developed by our group for the synthesis and functionalization of imidazo[1,2‐a]pyridines. Different synthetic strategies have been developed using easily accessible reactants for this purpose. We envisage that these newly developed protocols will be very useful for the synthesis of functionalized molecules bearing imidazo[1,2‐a]pyridine scaffolds. These strategies will also be attractive for the construction of other pharmaceutically important heterocycles.
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Adinath Majee Shrishnu Kumar KunduSougata Santra Alakananda Hajra 《Tetrahedron letters》2012,53(33):4433-4435
A new method for oxidation of alcohols to carbonyl compounds has been developed using NH2OH·HCl and NaIO4 under mild reaction conditions at room temperature. Application of the method for the synthesis of diiodo compound from α,β-unsaturated carbonyl compound is also described. 相似文献
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Matiur Rahman Anirban SarkarMonoranjan Ghosh Adinath Majee Alakananda Hajra 《Tetrahedron letters》2014
Benzoquinazolin-2-one derivatives were synthesized by using a catalytic amount of task specific ionic liquid, [1-methyl-3-(4-sulfobutyl)imidazolium-4-methylbenzenesulfonate] through a one-pot multicomponent Biginelli reaction of α-tetralone, aldehyde, and urea/thiourea in excellent yields within a short reaction time. Mechanism studies suggest that the reaction proceeds through iminium intermediate and C2-H of the TSIL plays a major role on its catalytic activity. The catalyst has been reused four times without any significant loss in catalytic activity. Large scale reaction by using this TSIL suggests the applicability of this methodology for bulk synthesis of quinazolinone derivatives. 相似文献
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Direct alkenylation of indoles at the 3-position with 1,3-dicarbonyl compounds under Brønsted acidic ionic liquid catalysis has been developed. The yields were excellent, and the catalyst can be reused at least six times without noticeable loss of catalytic activity. 相似文献
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