Microwave Accelerated Aza-Claisen Rearrangement by Eva Gajdošíková, Miroslava Martinková, Jozef Gonda, Patrik Conka

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Claisen Rearrangement Toward Cyclic Compound on Different Organic Synthesis Methods: Short Review by Rizki Rachmad Saputra, Reny Rosalina, Dimas Pramudita, Oktavia Rahmi Wulandari, Yuneta Yuneta, Amanda Natania Gracia, Tina Sugiyani, Marsya Imelya

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Selective C‐7 Functionalization of Phenanthridines by Microwave‐Assisted Claisen Rearrangements of 8‐Allyloxyphenanthridines by Mathias Ryslett Lepsøe, Aleksander Granum Dalevold, Prof. Dr. Lise‐Lotte Gundersen

Subjects: “…Claisen rearrangement…”
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Base-Mediated Claisen Rearrangement of CF₃-Containing Bisallyl Ethers by Yoko Hamada, Rio Matsunaga, Tomoko Kawasaki-Takasuka, Takashi Yamazaki

Subjects: “…Claisen rearrangement…”
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Reshuffle Bonds by Ball Milling: A Mechanochemical Protocol for Charge-Accelerated Aza-Claisen Rearrangements by Christian Schumacher, Lieselotte Fritz, Lena M. Hanek, Vitali Sidorin, Daniel Brüx, Carsten Bolm

Subjects: “…Claisen rearrangement…”
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THE ELABORATION OF EFFECTIVE METHODS OF SYNTHESIS OF NEW HETEROCYCLIC COMPOUNDS CONTAINING NIYROGEN AND CHALCOGEN WITH POTENTIAL BIOLOGICAL ACTIVITY by V. A. Potapov, D. A. Malinovich, S. V. Amosova

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Synthesis of Dihydrooxepino[3,2-c]Pyrazoles via Claisen Rearrangement and Ring-Closing Metathesis from 4-Allyloxy-1H-pyrazoles by Yoshihide Usami, Aoi Kohno, Hiroki Yoneyama, Shinya Harusawa

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Synthesis and late stage modifications of Cyl derivatives by Phil Servatius, Uli Kazmaier

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Formal Total Synthesis of Salvinorin A by Marc Halang, Prof. Dr. Martin E. Maier

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Synthesis of Indoloquinolines: An Intramolecular Cyclization Leading to Advanced Perophoramidine-Relevant Intermediates by Craig A. Johnston, David B. Cordes, Tomas Lebl, Alexandra M. Z. Slawin, Nicholas J. Westwood

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Recent Advances in Catalytic [3,3]-Sigmatropic Rearrangements by Huijin Lee, Ki Tae Kim, Min Kim, Cheoljae Kim

Subjects: “…Claisen rearrangement…”
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Claisen, Cope and Related Rearrangements in the Synthesis of Flavour and Fragrance Compounds by Janusz Nowicki

Subjects: “…Claisen rearrangements…”
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Synthesis and Modeling of Ezetimibe Analogues by Mateo M. Salgado, Alejandro Manchado, Carlos T. Nieto, David Díez, Narciso M. Garrido

“…The route involves a domino process: allylic acetate rearrangement, stereoselective Ireland–Claisen rearrangement and asymmetric Michael addition, which provides a δ-amino acid derivative with full stereochemical control. …”
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Photoredox-catalyzed diastereoselective dearomative prenylation and reverse-prenylation of electron-deficient indole derivatives by Xuexue Chang, Fangqing Zhang, Shibo Zhu, Zhuang Yang, Xiaoming Feng, Yangbin Liu

“…Herein, a photoredox-catalyzed tandem Giese radical addition/Ireland–Claisen rearrangement is disclosed. Diastereoselective dearomative prenylation and reverse-prenylation of electron-deficient indoles proceed smoothly under mild conditions. …”
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Synthesis of 7,2′-Dihydroxy-4′,5′-Dimethoxyisoflavanone, a Phytoestrogen with Derma Papilla Cell Proliferative Activity by Taewoo Kim, Hyun Su Kim, Jaebong Jang, Dong-Jun Kim, Jongkook Lee, Dongjoo Lee, Seok-Ho Kim

“…The key features of the synthesis include the construction of the deoxybenzoin unit through a sequence of Claisen rearrangement, oxidative cleavage, and aryllithium addition and the efficient synthesis of the isoflavanone architecture from highly functionalized 2-hydroxyketone.…”
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Total Synthesis and Anti-Inflammatory Evaluation of Osajin, Scandenone and Analogues by Rui Wang, Ran Ma, Ke Feng, Hongchen Lu, Wei Zhao, Hongzhen Jin

“…The key synthetic steps include aldol/intramolecular iodoetherification/elimination sequence reactions and a Suzuki coupling reaction to assemble the tricyclic core, chemoselective propargylation and Claisen rearrangement reactions to obtain natural compounds. …”
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Synthetic Potential of Regio- and Stereoselective Ring Expansion Reactions of Six-Membered Carbo- and Heterocyclic Ring Systems: A Review by Rida Noor, Ameer Fawad Zahoor, Asim Mansha, Samreen Gul Khan, Atta Ul Haq, Sajjad Ahmad, Sami A. Al-Hussain, Ali Irfan, Magdi E. A. Zaki

“…Numerous rearrangement and cycloaddition reactions involving Tiffeneau–Demjanov rearrangement, Aza–Claisen rearrangement, Schmidt rearrangement, Beckmann rearrangement, etc., have been described in this regard.…”
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Total Synthesis of Lineaflavones A, C, D, and Analogues by Rui Wang, Yu Fu, Ran Ma, Hongzhen Jin, Wei Zhao

“…The key synthetic steps include aldol/oxa-Michael/dehydration sequence reactions to assemble the tricyclic core, Claisen rearrangement and Schenck ene reaction to construct the key intermediate, and selective substitution or elimination of tertiary allylic alcohol to obtain natural compounds. …”
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Synthesis and Biological Evaluation of Substituted Fused Dipyranoquinolinones by Evangelia-Eirini N. Vlachou, Eleni Pontiki, Dimitra J. Hadjipavlou-Litina, Konstantinos E. Litinas

“…In the absence of gold nanoparticles, the methyl-substituted propargyloxycoumarin derivatives resulted in fused furopyranoquinolinones through Claisen rearrangement and <i>5-exo-dig</i> cyclization. The intermediate propargyloxy-fused pyridocoumarins are prepared by propargylation of the corresponding hydroxy-fused pyridocoumarins. …”
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Exploring the Mechanism of Catalysis with the Unified Reaction Valley Approach (URVA)—A Review by Elfi Kraka, Wenli Zou, Yunwen Tao, Marek Freindorf

“…After presenting the theoretical background of URVA, we discuss its application to four diverse catalytic processes: (i) the Rh catalyzed methanol carbonylation—the Monsanto process; (ii) the Sharpless epoxidation of allylic alcohols—transition to heterogenous catalysis; (iii) Au(I) assisted [3,3]-sigmatropic rearrangement of allyl acetate; and (iv) the <i>Bacillus subtilis</i> chorismate mutase catalyzed Claisen rearrangement—and show how URVA leads to a new protocol for fine-tuning of existing catalysts and the design of new efficient and eco-friendly catalysts. …”
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