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Journal articles on the topic 'Radical one carbon homologation'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 February 2022

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1

Hart, David J., and Franklin L. Seely. "Bis(trimethylstannyl)benzopinacolate-mediated intermolecular free-radical carbon-carbon bond-forming reactions: a new one-carbon homologation." Journal of the American Chemical Society 110, no. 5 (1988): 1631–33. http://dx.doi.org/10.1021/ja00213a051.

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2

Taber, Douglass F., Craig M. Paquette, and P. Ganapati Reddy. "One carbon homologation of halides to benzyl ethers." Tetrahedron Letters 50, no. 21 (2009): 2462–63. http://dx.doi.org/10.1016/j.tetlet.2009.03.010.

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3

Imamoto, Tsuneo, Yasuo Kamiya, Toshihiko Hatajima, and Harumi Takahashi. "Tandem one-carbon homologation of esters to cyclopropanols." Tetrahedron Letters 30, no. 38 (1989): 5149–52. http://dx.doi.org/10.1016/s0040-4039(01)93471-9.

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4

Lebel, Hélène, and Chehla Ladjel. "Reductive One-Carbon Homologation of Aldehydes and Ketones." Journal of Organic Chemistry 70, no. 24 (2005): 10159–61. http://dx.doi.org/10.1021/jo0516741.

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5

Sebastian, Sharol, Monika, Anil Kumar Khatana, Eqvinshi Yadav, and Manoj K. Gupta. "Recent approaches towards one-carbon homologation–functionalization of aldehydes." Organic & Biomolecular Chemistry 19, no. 14 (2021): 3055–74. http://dx.doi.org/10.1039/d1ob00135c.

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6

Marco-Contelles, José, and Elsa de Opazo. "SOME UNEXPECTED RESULTS IN DONDONI'S ONE-CARBON HOMOLOGATION PROCEDURE1." Journal of Carbohydrate Chemistry 20, no. 7&8 (2001): 637–46. http://dx.doi.org/10.1081/car-100108278.

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7

Huffman, John W., Ming Jung Wu, and H. Howard Joyner. "Regioselective synthesis of 1-formylcyclohexenes by one-carbon homologation." Journal of Organic Chemistry 56, no. 17 (1991): 5224–26. http://dx.doi.org/10.1021/jo00017a045.

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8

Bonne, Damien, Mouloud Dekhane, and Jieping Zhu. "Mild Oxidative One-Carbon Homologation of Aldehyde to Amide." Journal of the American Chemical Society 127, no. 19 (2005): 6926–27. http://dx.doi.org/10.1021/ja0511220.

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9

Dixon, D. D., and W. F. Burgoyne. "Nitriles from olefins and ammonia via one-carbon homologation." Applied Catalysis 20, no. 1-2 (1986): 79–90. http://dx.doi.org/10.1016/0166-9834(86)80007-0.

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10

Barton, Derek H. R., and Wansheng Liu. "Two Carbon Homologation of Carboxylic Acids Using Acrylamide as a Radical Trap." Tetrahedron Letters 38, no. 14 (1997): 2431–34. http://dx.doi.org/10.1016/s0040-4039(97)00418-8.

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11

Mondal, Shovan, Malek Nechab, Nicolas Vanthuyne, and Michèle P. Bertrand. "One-pot Crabbé homologation-radical cascade cyclisation with memory of chirality." Chemical Communications 48, no. 19 (2012): 2549. http://dx.doi.org/10.1039/c2cc17830c.

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12

Barton, DHR, CY Chern, and JC Jaszberenyi. "The Invention of Radical Reactions. XXXIII. Homologation Reactions of Carboxylic Acids by Radical Chain Chemistry." Australian Journal of Chemistry 48, no. 2 (1995): 407. http://dx.doi.org/10.1071/ch9950407.

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13

Nemoto, Hisao. "MAC reagents. Three-components Coupling Reaction with One Carbon Homologation." Journal of Synthetic Organic Chemistry, Japan 62, no. 4 (2004): 347–54. http://dx.doi.org/10.5059/yukigoseikyokaishi.62.347.

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14

Katritzky, Alan, Srinivasa Tala та Sandeep Singh. "One-Carbon Homologation of Aldehydes to N-(α-Haloacyl)benzotriazoles". Synthesis 2006, № 19 (2006): 3231–37. http://dx.doi.org/10.1055/s-2006-950183.

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15

Shen, Wang, and Aaron Kunzer. "A Facile One-Carbon Homologation of Aryl Aldehydes to Amides." Organic Letters 4, no. 8 (2002): 1315–17. http://dx.doi.org/10.1021/ol025608m.

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16

Li, Zhexi, Manoj K. Gupta, and Timothy S. Snowden. "One-Carbon Homologation of Primary Alcohols and the Reductive Homologation of Aldehydes Involving a Jocic-Type Reaction." European Journal of Organic Chemistry 2015, no. 32 (2015): 7009–19. http://dx.doi.org/10.1002/ejoc.201501089.

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17

BARTON, D. H. R., and W. LIU. "ChemInform Abstract: Two-Carbon Homologation of Carboxylic Acids Using Acrylamide as a Radical Trap." ChemInform 28, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199729123.

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18

Hodgson, David M., Matthew J. Fleming, and Steven J. Stanway. "One-Carbon Homologation ofN-Sulfonylaziridines to Allylic Amines Using Dimethylsulfonium Methylide." Organic Letters 7, no. 15 (2005): 3295–98. http://dx.doi.org/10.1021/ol051124p.

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19

Yoshida, Jun-ichi, Shin-ichiro Matsunaga, Toshiki Murata, and Sachihiko Isoe. "New one carbon homologation reagents utilizing electrochemical oxidation of organosilicon compounds." Tetrahedron 47, no. 4-5 (1991): 615–24. http://dx.doi.org/10.1016/s0040-4020(01)87051-4.

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20

HUFFMAN, J. W., M. J. WU, and H. H. JOYNER. "ChemInform Abstract: Regioselective Synthesis of 1-Formylcyclohexenes by One-Carbon Homologation." ChemInform 23, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.199204123.

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21

Mondal, Shovan, Malek Nechab, Nicolas Vanthuyne, and Michele P. Bertrand. "ChemInform Abstract: One-Pot Crabbe Homologation-Radical Cascade Cyclization with Memory of Chirality." ChemInform 43, no. 27 (2012): no. http://dx.doi.org/10.1002/chin.201227158.

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22

Li, Zhexi, Manoj K. Gupta, and Timothy S. Snowden. "ChemInform Abstract: One-Carbon Homologation of Primary Alcohols and the Reductive Homologation of Aldehydes Involving a Jocic-Type Reaction." ChemInform 47, no. 9 (2016): no. http://dx.doi.org/10.1002/chin.201609099.

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23

Wang, Lei, Pinhua Li, Jincan Yan, and Zhongzhi Wu. "A novel preparation of methyl ketones through one-carbon homologation of aldehydes." Tetrahedron Letters 44, no. 25 (2003): 4685–88. http://dx.doi.org/10.1016/s0040-4039(03)01084-0.

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24

Shen, Wang, and Aaron Kunzer. "ChemInform Abstract: A Facile One-Carbon Homologation of Aryl Aldehydes to Amides." ChemInform 33, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.200233096.

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25

Marco-Contelles, Jose, and Elsa de Opazo. "ChemInform Abstract: Some Unexpected Results in Dondoni′s One-Carbon Homologation Procedure." ChemInform 33, no. 19 (2010): no. http://dx.doi.org/10.1002/chin.200219199.

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26

Xu, Jianyu, J. Cameron Twitty, and Mary P. Watson. "Nickel-Catalyzed Deaminative Cyanation: Nitriles and One-Carbon Homologation from Alkyl Amines." Organic Letters 23, no. 16 (2021): 6242–45. http://dx.doi.org/10.1021/acs.orglett.1c01959.

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27

NARASIMHAN, S., H. MOHAN, and S. MADHAVAN. "ChemInform Abstract: One-Carbon Homologation of 10-Undecenyl Derivatives Through Peroxide- Catalyzed Addition of Carbon Tetrachloride." ChemInform 26, no. 52 (2010): no. http://dx.doi.org/10.1002/chin.199552079.

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28

Katritzky, Alan R., Rong Jiang, Geoffroy L. Sommen, and Sandeep K. Singh. "One-carbon homologation of aryl and alkyl aldehydes to amides using BtCH2P+Ph3C-." Arkivoc 2004, no. 9 (2004): 44–51. http://dx.doi.org/10.3998/ark.5550190.0005.907.

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29

Stevens, Anne T., Mino R. Caira, James R. Bull, and Kelly Chibale. "Cycloaddition and one-carbon homologation studies in the synthesis of advanced iridoid precursors." Organic & Biomolecular Chemistry 7, no. 17 (2009): 3527. http://dx.doi.org/10.1039/b902452b.

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30

Hahn, Roger C., and Jan Tompkins. "One-pot, one- and multi-carbon homologation of alkyl halides; reaction of grignard reagents with chloroiodomethane." Tetrahedron Letters 31, no. 7 (1990): 937–40. http://dx.doi.org/10.1016/s0040-4039(00)94397-1.

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31

Kim, Mikhail, Barbara Grzeszczyk, and Aleksander Zamojski. "Improving the stereoselectivity of one-carbon atom homologation of hexoses at the terminal position." Tetrahedron Letters 43, no. 7 (2002): 1337–40. http://dx.doi.org/10.1016/s0040-4039(01)02376-0.

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32

Santiago, Braulio, and A. I. Meyers. "Formamidine anions in synthesis. The one-carbon homologation of aldehydes and ketones to nitriles." Tetrahedron Letters 34, no. 37 (1993): 5839–42. http://dx.doi.org/10.1016/s0040-4039(00)73793-2.

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33

Tomioka, Takashi, Rambabu Sankranti, Tsuyoshi Yamada, and Courtney Clark. "n-BuLi/LiCH2CN-Mediated One-Carbon Homologation of Aryl Epoxides into Conjugated Allyl Alcohols." Organic Letters 15, no. 19 (2013): 5099–101. http://dx.doi.org/10.1021/ol402466y.

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34

Yoshida, Junichi, Shinichiro Matsunaga, Yuji Ishichi, Tsuyoshi Maekawa, and Sachihiko Isoe. "A new method for the synthesis of acylsilanes via one-carbon homologation of aldehydes." Journal of Organic Chemistry 56, no. 3 (1991): 1307–9. http://dx.doi.org/10.1021/jo00003a072.

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35

Mink, Daniel, та Ghislain Deslongchamps. "An Improved Method for the One-Carbon Homologation of Ketones with Acidic α-Hydrogens". Synlett 1996, № 09 (1996): 875–76. http://dx.doi.org/10.1055/s-1996-5616.

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36

Horváth, András, Koen De Smet, Dominic Ormerod, et al. "Development of the One-Carbon Homologation of a 4-Methylcoumarin Assisted by In-Line FTIR." Organic Process Research & Development 9, no. 3 (2005): 356–59. http://dx.doi.org/10.1021/op049787u.

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37

Wu, Chaoqiang, Guojiao Wu, Yan Zhang, and Jianbo Wang. "One-carbon homologation of arylboronic acids: a convenient approach to the synthesis of pinacol benzylboronates." Organic Chemistry Frontiers 3, no. 7 (2016): 817–22. http://dx.doi.org/10.1039/c6qo00141f.

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38

Katritzky, Alan R., Zhijun Yang та Jean-Luc Moutou. "Conversion of aldehydes to α-acetoxymethyl ketones: One-carbon homologation with (benzotriazol-1-yl)phenoxymethane". Tetrahedron Letters 36, № 6 (1995): 841–44. http://dx.doi.org/10.1016/0040-4039(94)02395-r.

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39

Van Hijfte, Luc, Michael Kolb, and Pascale Witz. "A practical procedure for the conversion of aldehydes to terminal alkynes by a one carbon homologation." Tetrahedron Letters 30, no. 28 (1989): 3655–56. http://dx.doi.org/10.1016/s0040-4039(01)80473-1.

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40

Yoo, Jae Won, Youngran Seo, Jong Beom Park, and Young Gyu Kim. "Two-way homologation of aliphatic aldehydes: Both one-carbon shortening and lengthening via the same intermediate." Tetrahedron 76, no. 6 (2020): 130883. http://dx.doi.org/10.1016/j.tet.2019.130883.

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41

Satoh, Tsuyoshi, Yasumasa Hayashi, Yasuhiro Mizu та Koji Yamakawa. "α-Sulfinyl carbenoid: One-carbon homologation of ketones to α-sulfinyl ketones using chloromethyl phenyl sulfoxide". Tetrahedron Letters 33, № 47 (1992): 7181–84. http://dx.doi.org/10.1016/s0040-4039(00)60867-5.

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42

Katritzky, Alan R., Suoming Zhang, Abdel Haleem Mostafa Hussein, Yunfeng Fang, and Peter J. Steel. "One-Carbon Homologation of Carboxylic Acids via BtCH2TMS: A Safe Alternative to the Arndt−Eistert Reaction." Journal of Organic Chemistry 66, no. 16 (2001): 5606–12. http://dx.doi.org/10.1021/jo0017640.

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43

Dasgupta, Ratna, та Usha Ranjan Ghatak. "A simple synthesis of α, β-unsaturated aldehydes by 1,3-carbonyl transposition through one carbon homologation". Tetrahedron Letters 26, № 12 (1985): 1581–84. http://dx.doi.org/10.1016/s0040-4039(00)98557-5.

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44

Satoh, Tsuyoshi, та Kohsuke Miyashita. "A new synthesis of α,α-disubstituted carbonyl compounds from carbonyl compounds with one-carbon homologation". Tetrahedron Letters 45, № 25 (2004): 4859–64. http://dx.doi.org/10.1016/j.tetlet.2004.04.154.

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45

SANTIAGO, B., and A. I. MEYERS. "ChemInform Abstract: Formamidine Anions in Synthesis. The One-Carbon Homologation of Aldehydes and Ketones to Nitriles." ChemInform 25, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.199404124.

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46

MINK, D., та G. DESLONGCHAMPS. "ChemInform Abstract: An Improved Method for the One-Carbon Homologation of Ketones with Acidic α-Hydrogens." ChemInform 28, № 7 (2010): no. http://dx.doi.org/10.1002/chin.199707164.

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47

Tomioka, Takashi, Rambabu Sankranti, Tsuyoshi Yamada, and Courtney Clark. "ChemInform Abstract: n-BuLi/LiCH2CN-Mediated One-Carbon Homologation of Aryl Epoxides into Conjugated Allyl Alcohols." ChemInform 45, no. 10 (2014): no. http://dx.doi.org/10.1002/chin.201410048.

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48

YOSHIDA, J., S. MATSUNAGA, Y. ISHICHI, T. MAEKAWA, and S. ISOE. "ChemInform Abstract: A New Method for the Synthesis of Acylsilanes via One-Carbon Homologation of Aldehydes." ChemInform 22, no. 25 (2010): no. http://dx.doi.org/10.1002/chin.199125198.

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49

Studer, Armido, and Antonio J. Herrera. "1,3-Dithiane-Derived Alkoxyamines as One-Carbon Radical Precursors." Synthesis, no. 9 (2005): 1389–96. http://dx.doi.org/10.1055/s-2005-865288.

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50

Murahashi, Shun-Ichi, Yasushi Imada та Koichi Nishimura. "Palladium-catalyzed Carbonylation of Allylamines. Synthesis of β,γ-unsaturated amides by one-carbon homologation of Allylamines". Tetrahedron 50, № 2 (1994): 453–64. http://dx.doi.org/10.1016/s0040-4020(01)80767-5.

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