A Domino Copper-Catalyzed C−O Coupling−Claisen Rearrangement Process

Gero Nordmann; Stephen L. Buchwald

doi:10.1021/ja034809y

A Domino Copper-Catalyzed C−O Coupling−Claisen Rearrangement Process

Journal of the American Chemical Society ◽

10.1021/ja034809y ◽

2003 ◽

Vol 125 (17) ◽

pp. 4978-4979 ◽

Cited By ~ 136

Author(s):

Gero Nordmann ◽

Stephen L. Buchwald

Keyword(s):

Claisen Rearrangement ◽

Rearrangement Process

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ChemInform Abstract: Asymmetric Synthesis of Seven-Membered Carbocyclic Rings via a Sequential Oxyanionic 5-Exo-Dig Cyclization/Claisen Rearrangement Process. Total Synthesis of (-)-Frondosin B.

ChemInform ◽

10.1002/chin.200945062 ◽

2009 ◽

Vol 40 (45) ◽

Author(s):

Timo V. Ovaska ◽

Jonathan A. Sullivan ◽

Sami I. Ovaska ◽

Jacob B. Winegrad ◽

Justin D. Fair

Keyword(s):

Total Synthesis ◽

Asymmetric Synthesis ◽

Claisen Rearrangement ◽

Rearrangement Process ◽

Frondosin B ◽

Carbocyclic Rings

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Synthesis of Seven-Membered Carbocyclic Rings via a Microwave-Assisted Tandem Oxyanionic 5-exodigCyclization−Claisen Rearrangement Process

The Journal of Organic Chemistry ◽

10.1021/jo0710432 ◽

2007 ◽

Vol 72 (17) ◽

pp. 6624-6627 ◽

Cited By ~ 10

Author(s):

Xin Li ◽

Robert E. Kyne ◽

Timo V. Ovaska

Keyword(s):

Claisen Rearrangement ◽

Microwave Assisted ◽

Rearrangement Process ◽

Carbocyclic Rings

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Facile access to 2,2-disubstituted indolin-3-ones via a cascade Fischer indolization/Claisen rearrangement reaction

Chemical Communications ◽

10.1039/c7cc03754f ◽

2017 ◽

Vol 53 (54) ◽

pp. 7485-7488 ◽

Cited By ~ 17

Author(s):

Zilei Xia ◽

Jiadong Hu ◽

Yu-Qi Gao ◽

Qizheng Yao ◽

Weiqing Xie

Keyword(s):

Claisen Rearrangement ◽

Fischer Indolization ◽

Rearrangement Process ◽

Rearrangement Reaction

From readily accessible arylhydrazines and allyloxyketones, 2,2-disubstituted indolin-3-ones could be obtained in good to excellent yields via a cascade Fischer indolization/Claisen rearrangement process.

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ChemInform Abstract: Iminophosphorane-Mediated One-Pot Conversion of Allyl Azides into α-Allylated Nitriles by a Consecutive Staudinger Reaction/Aza-Wittig Reaction/3-Aza-Claisen Rearrangement Process.

ChemInform ◽

10.1002/chin.199219142 ◽

2010 ◽

Vol 23 (19) ◽

pp. no-no

Author(s):

P. MOLINA ◽

M. ALAJARIN ◽

C. LOPEZ-LEONARDO

Keyword(s):

Wittig Reaction ◽

Claisen Rearrangement ◽

Staudinger Reaction ◽

One Pot ◽

Rearrangement Process

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Asymmetric Synthesis of Seven-Membered Carbocyclic Rings via a Sequential Oxyanionic 5-Exo-Dig Cyclization/Claisen Rearrangement Process. Total Synthesis of (−)-Frondosin B

Organic Letters ◽

10.1021/ol900967j ◽

2009 ◽

Vol 11 (12) ◽

pp. 2715-2718 ◽

Cited By ~ 44

Author(s):

Timo V. Ovaska ◽

Jonathan A. Sullivan ◽

Sami I. Ovaska ◽

Jacob B. Winegrad ◽

Justin D. Fair

Keyword(s):

Total Synthesis ◽

Asymmetric Synthesis ◽

Claisen Rearrangement ◽

Rearrangement Process ◽

Frondosin B ◽

Carbocyclic Rings

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Iminophosphorane-mediated one-pot conversion of allyl azides into α-allylated nitriles by a consecutive staudinger reaction/ aza-wittig reaction/3-aza-claisen rearrangement process

Tetrahedron Letters ◽

10.1016/0040-4039(91)80623-e ◽

1991 ◽

Vol 32 (32) ◽

pp. 4041-4044 ◽

Cited By ~ 15

Author(s):

Pedro Molina ◽

Mateo Alajarin ◽

Carmen Lopez-Leonardo

Keyword(s):

Wittig Reaction ◽

Claisen Rearrangement ◽

Staudinger Reaction ◽

One Pot ◽

Rearrangement Process

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Synthesis of cycloheptanoid natural products via tandem 5-exo cyclization/Claisen rearrangement process

ARKIVOC ◽

10.3998/ark.5550190.0012.505 ◽

2010 ◽

Vol 2011 (5) ◽

pp. 34-44

Author(s):

Timo V. Ovaska

Keyword(s):

Natural Products ◽

Claisen Rearrangement ◽

Rearrangement Process

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ChemInform Abstract: Synthesis of Seven-Membered Carbocyclic Rings via a Microwave-Assisted Tandem Oxyanionic 5-exo Dig Cyclization—Claisen Rearrangement Process.

ChemInform ◽

10.1002/chin.200801059 ◽

2008 ◽

Vol 39 (1) ◽

Author(s):

Xin Li ◽

Robert E. Kyne ◽

Timo V. Ovaska

Keyword(s):

Claisen Rearrangement ◽

Microwave Assisted ◽

Rearrangement Process ◽

Carbocyclic Rings

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ChemInform Abstract: Synthesis of Cycloheptanoid Natural Products via a Tandem 5-exo-Cyclization/Claisen Rearrangement Process

ChemInform ◽

10.1002/chin.201110248 ◽

2011 ◽

Vol 42 (10) ◽

pp. no-no ◽

Cited By ~ 1

Author(s):

Timo V. Ovaska

Keyword(s):

Natural Products ◽

Claisen Rearrangement ◽

Rearrangement Process

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Microwave-assisted organic syntheses: microwave effect on intramolecular reactions – the Claisen rearrangement of allylphenyl ether and 1-allyloxy-4-methoxybenzene

RSC Advances ◽

10.1039/c5ra18039b ◽

2015 ◽

Vol 5 (110) ◽

pp. 90272-90280 ◽

Cited By ~ 10

Author(s):

Satoshi Horikoshi ◽

Tomoki Watanabe ◽

Momoko Kamata ◽

Yumiko Suzuki ◽

Nick Serpone

Keyword(s):

Microwave Irradiation ◽

Claisen Rearrangement ◽

Solvent Free ◽

Microwave Assisted ◽

Organic Syntheses ◽

Microwave Effect ◽

Intramolecular Reactions ◽

Rearrangement Process

We examined the possible effect microwaves may have on intramolecular reactions such as the Claisen-type rearrangement process carried out in DMSO solvent and in solvent-free microwave irradiation conditions.

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