A new and simple approach for the synthesis of 3-acetyl-3,4-dihydro-1(2H)-naphthalenones and 3,4-dihydro-3-(2-methyl-1,3-dithiolan-2-yl)-1(2H)-naphthalenones

N. A. Kudav; (Miss) M. D. Kulkarni; D. A. Kochrekar

首页> 外文期刊>Journal of the Indian Chemical Society >A new and simple approach for the synthesis of 3-acetyl-3,4-dihydro-1(2H)-naphthalenones and 3,4-dihydro-3-(2-methyl-1,3-dithiolan-2-yl)-1(2H)-naphthalenones

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A new and simple approach for the synthesis of 3-acetyl-3,4-dihydro-1(2H)-naphthalenones and 3,4-dihydro-3-(2-methyl-1,3-dithiolan-2-yl)-1(2H)-naphthalenones

机译：一种合成3-乙酰基-3,4-二氢-1（2H）-萘烯酮和3,4-二氢-3-（2-甲基-1,3-二硫代-2-基）-的新方法1（2H）-萘

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3-Acetyl-3,4-dihydro-1(2H)-naphthalenones and 3,4-dihydro-3-(2-methyl-1,3-dithiolan-2-yl)-1(2H)-naphthalenones are prepared using levulinic acid as starting substrate.

机译：使用以下方法制备3-乙酰基-3,4-二氢-1（2H）-萘酮和3,4-二氢-3-（2-甲基-1,3-二硫代-2-基）-1（2H）-萘酮乙酰丙酸为起始底物。

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《Journal of the Indian Chemical Society》 |2002年第1期|共3页
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N. A. Kudav; (Miss) M. D. Kulkarni; D. A. Kochrekar;
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1. A new and simple approach for the synthesis of 3-acetyl-3,4-dihydro-1(2H)-naphthalenones and 3,4-dihydro-3-(2-methyl-1,3-dithiolan-2-yl)-1(2H)-naphthalenones [J] . N. A. Kudav, (Miss) M. D. Kulkarni, D. A. Kochrekar Journal of the Indian Chemical Society . 2002,第1期

机译：一种合成3-乙酰基-3,4-二氢-1（2H）-萘烯酮和3,4-二氢-3-（2-甲基-1,3-二硫代-2-基）-的新方法1（2H）-萘
2. Isolation and Characterization of 5,6-Dimethoxy-1,2,3,4-tetrahydro-2(1H)-naphthalenone from Catalytic Reductions of the Respective 2-Amino-, and 2-Nitro-3,4-dihydro-5,6-dimethoxy-1(2H)-naphthalenone [J] . Jack C. Kim Journal of the Korean Chemical Society . 1979,第2期

机译：从2-氨基-和2-硝基-3,4-二氢-5的催化还原中分离和表征5,6-二甲氧基-1,2,3,4-四氢-2（1H）-萘酮6-二甲氧基-1（2H）-萘酮
3. Mechanistic Pathways in the Transformation Product of 5,6-Dimethoxy-1,2,3,4-tetrahydro-2(1H)naphthalenone from the Respective 2-amino and, 2-Nitro-3,4-dihydro-5,6-dimethoxy-1(2H)naphthalenone. A Correction [J] . Jack C. Kim Journal of the Korean Chemical Society . 1979,第4期

机译：来自各自的2-氨基和2-硝基-3,4-二氢-5,6-的5,6-二甲氧基-1,2,3,4-四氢-2（1H）萘酮转化产物的机理途径二甲氧基-1（2H）萘酮。更正
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6. Rhodium(III)-Catalyzed 4+2 Annulation via C-H Activation: Synthesis of Multi-Substituted Naphthalenone Sulfoxonium Ylides [O] . Xiaohan Song, Xu Han, Rui Zhang, 2019

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7. SYNTHESIS, CHARACTERIZATION AND ANTIFUNGAL ACTIVITY OF QUINAZOLINE THIONE DERIVATIVES OF 3, 4-DIHYDRO-1(2H)-NAPHTHALENONE [O] . Sandeep Arora, Badri Prakash Nagori 2014

机译：喹唑啉酮衍生物的合成，表征和抗真菌活性为3,4-二氢-1（2H） - 萘酮
8. Grafting of 2 (2-Hydroxy-5-Vinylphenyl) 2H-Benzotriazole onto Polymers with Aliphatic Groups. Synthesis and Polymerization of 2 (2-Hydroxy-5-Isopropenylphenyl) 2H-Benzotriazole and a New Synthesis of 2 (2-Hydroxy-5-Vinylphenyl) 2H [R] . Pradellok, W., Nir, Z., Vogl, O. 1981

机译：将2（2-羟基-5-乙烯基苯基）2H-苯并三唑接枝到具有脂族基团的聚合物上。 2（2-羟基-5-异丙烯基苯基）2H-苯并三唑的合成与聚合及2（2-羟基-5-乙烯基苯基）2H的新合成

A new and simple approach for the synthesis of 3-acetyl-3,4-dihydro-1(2H)-naphthalenones and 3,4-dihydro-3-(2-methyl-1,3-dithiolan-2-yl)-1(2H)-naphthalenones

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