Photochemistry and Organic Synthesis

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Find more information on the Altmetric Attention Score and how the score is calculated. View Author Information. Cite this: Chem. Article Views Altmetric -. Citations Note: In lieu of an abstract, this is the article's first page. Cited By. This article is cited by publications. Tkachenko, Taku Hasobe. Journal of the American Chemical Society , 37 , DOI: Asymmetric Synthesis of Boryl-Functionalized Cyclobutanols. Inorganic Chemistry , 58 17 , Stereocontrolled Preparation of Diversely Trifunctionalized Cyclobutanes.

The Journal of Organic Chemistry , 84 16 , Francis, Brian S. Newell, Haobin Wang, Marino J. The Journal of Organic Chemistry , 84 15 , Chemical Reviews , 12 , Mattia Silvi, Varinder K. Journal of the American Chemical Society , 24 , Strauss, Hermann A. Organic Letters , 21 11 , Daniel M. Flores, Valerie A. Journal of the American Chemical Society , 22 , Monish A. The Journal of Organic Chemistry , 84 9 , Journal of the American Chemical Society , 16 , Sai Reddy, Andrei G. Organic Letters , 21 8 , Journal of the American Chemical Society , 15 , Organic Letters , 21 7 , ACS Catalysis , 9 4 , Bencan Tang, Robert S.

Organic Letters , 21 5 , Graham Haun, Alyson N. Paneque, David W. Almond, Brooke E. Austin, Gustavo Moura-Letts. Luke D. Elliott, Kevin I. Noriyoshi Arai, Takeshi Ohkuma. Sachin G. The Journal of Organic Chemistry , 84 3 , The Journal of Physical Chemistry C , 50 , Photosensitization and Photocatalysis—Perspectives in Organic Synthesis. ACS Catalysis , 8 12 , Leiming Tian, Isaac J. Organic Letters , 20 21 , ACS Omega , 3 9 , Organic Letters , 20 18 , Evgeni M. Glebov, Natalia V. Ruban, Ivan P.


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    Skubi, Jesse B. Kidd, Hoimin Jung, Ilia A. Journal of the American Chemical Society , 47 , Synthesis of Benzoarylyl 2-hydroxyphenyl methanones via Photoinduced Rearrangement of E Arylvinyl-4H-chromenones. Organic Letters , 19 21 , Matthew B. Chemical Reviews , 18 , Ali T. The Journal of Organic Chemistry , 82 18 , The Journal of Organic Chemistry , 82 15 , Markus D. ACS Catalysis , 7 8 , Jiannan Zhao, Jonathan L.

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    Laboratory of Organic Synthesis and Photochemistry

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    Shaw, Jack Twilton, and David W. Photoredox Catalysis in Organic Chemistry. Journal of the American Chemical Society , 25 , Organic Letters , 18 9 , Superoxide Ion: Generation and Chemical Implications. Chemical Reviews , 5 , Elisa I. Carrera, Anabel E. Lanterna, Alan J. Lough, Juan C. Scaiano, and Dwight S. Journal of the American Chemical Society , 8 , Jian Luo and Jian Zhang.

    ACS Catalysis , 6 2 , Evgeny N. Ushakov, Artem I. Vedernikov, Natalia A. Lobova, Svetlana N. Dmitrieva, Lyudmila G. Moiseeva, Judith A. Howard, Michael V. Alfimov, and Sergey P. The Journal of Physical Chemistry A , 52 , Organic Letters , 17 24 , Andrey G. Lvov, Valerii Z. Shirinian, Alexey V. Zakharov, Mikhail M. Krayushkin, Vadim V. Kachala, and Igor V. The Journal of Organic Chemistry , 80 22 , The Journal of Organic Chemistry , 80 19 , Organometallics , 34 17 , Jacob A.

    Torres, and Jian Zhang. ACS Catalysis , 5 9 , Jochen Zoller, David C. Fabry, and Magnus Rueping. ACS Catalysis , 5 6 , Macromolecules , 48 9 , Michael L. Conner, Yao Xu, and M. Journal of the American Chemical Society , 10 , Laura Ruiz Espelt, Iain S. McPherson, Eric M. Wiensch, and Tehshik P.

    Journal of the American Chemical Society , 7 , Organic Letters , 17 4 , Marcus Wegmann and Thorsten Bach. The Journal of Organic Chemistry , 80 3 , Journal of the American Chemical Society , 4 , Stereoselective Preparation of Spiro[4. Organic Letters , 17 1 , Volume 61 Issue 12 Dec , pp. Volume 60 Issue 12 Dec , pp.

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    DOI: Oxidative degradation of alternative gasoline oxygenates in aqueous solution by ultrasonic irradiation: Mechanistic study. Microflow photo-radical reaction using a compact light source: application to the Barton reaction leading to a key intermediate for myriceric acid A. A new free radical route to oximes using alkyl halides, hexabutylditin and readily available nitrite esters. First total synthesis of xestobergsterol A and active structural analogues of the xestobergsterols.