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Journal articles on the topic 'One-pot procedure'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Scheffler, Ulf, and Rainer Mahrwald. "A One-Pot Cross-Pinacol Coupling/Rearrangement Procedure." Helvetica Chimica Acta 95, no. 10 (October 2012): 1970–75. http://dx.doi.org/10.1002/hlca.201200402.

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2

Bum Jang, Won, Won Suk Shin, Kilsung Lee, and Dong Young Oh. "Synthesis of β-Amino Phosphonates in One-Pot Procedure." Synthetic Communications 27, no. 23 (December 1997): 4101–5. http://dx.doi.org/10.1080/00397919708005457.

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3

Takahashi, Tamotsu, Baojian Shen, Kiyohiko Nakajima, and Zhenfeng Xi. "A Convenient One-Pot Procedure to Arylcyclobutenes from Arylacetylenes." Journal of Organic Chemistry 64, no. 23 (November 1999): 8706–8. http://dx.doi.org/10.1021/jo990596c.

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4

Severin, René, Jessica Reimer, and Sven Doye. "One-Pot Procedure for the Synthesis of Unsymmetrical Diarylalkynes." Journal of Organic Chemistry 75, no. 10 (May 21, 2010): 3518–21. http://dx.doi.org/10.1021/jo100460v.

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5

Cardinale, Jens, and Johannes Ermert. "Simplified synthesis of aryliodonium ylides by a one-pot procedure." Tetrahedron Letters 54, no. 16 (April 2013): 2067–69. http://dx.doi.org/10.1016/j.tetlet.2013.02.018.

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6

Jing, Xiaobi, Xin Pan, Zhen Li, Yaocheng Shi, and Chaoguo Yan. "Novel One-Pot Procedure for the Synthesis of 1,2-Diketones." Synthetic Communications 39, no. 3 (January 13, 2009): 492–96. http://dx.doi.org/10.1080/00397910802398264.

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7

Osuka, Atsuhiro, Ben-li Liu, and Kazuhiro Maruyama. "An Efficient One-Pot Synthetic Procedure of Multiple Porphyrin-Cyclization." Chemistry Letters 22, no. 6 (June 1993): 949–52. http://dx.doi.org/10.1246/cl.1993.949.

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8

Antane, Schuyler, Ronald Bernotas, Yanfang Li, Robert McDevitt, and Yinfa Yan. "Chloromethyl Sulfones from Sulfonyl Chlorides via a One‐Pot Procedure." Synthetic Communications 34, no. 13 (January 1, 2004): 2443–49. http://dx.doi.org/10.1081/scc-120039498.

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9

Wu, Jishan, Chunyan Chi, Xianhong Wang, Ji Li, Xiaojiang Zhao, and Fosong Wang. "A One-Pot Procedure to Prepare S-Protected 4-Iodothiophenols." Synthetic Communications 30, no. 23 (December 2000): 4293–98. http://dx.doi.org/10.1080/00397910008087051.

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10

Meyer-Wegner, Frank, Stefan Scholz, Inge Sänger, Frauke Schödel, Michael Bolte, Matthias Wagner, and Hans-Wolfram Lerner. "Synthesis of Wiberg’s Tetrasilatetrahedrane (tBu3Si)4Si4by a One-Pot Procedure." Organometallics 28, no. 23 (December 14, 2009): 6835–37. http://dx.doi.org/10.1021/om900763y.

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11

Hogrefe, Richard I., Morteza M. Vaghefi, Mark A. Reynolds, Kevin M. Young, and Lyle J. Arnold. "Deprotection of methylphosphonate oligonucleotides using a novel one-pot procedure." Nucleic Acids Research 21, no. 9 (1993): 2031–38. http://dx.doi.org/10.1093/nar/21.9.2031.

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12

Scheffler, Ulf, and Rainer Mahrwald. "ChemInform Abstract: A One-Pot Cross-Pinacol Coupling/Rearrangement Procedure." ChemInform 44, no. 10 (March 5, 2013): no. http://dx.doi.org/10.1002/chin.201310038.

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13

van der Heijden, Gydo, Jasper Kraakman, Jasper Biemolt, Eelco Ruijter, and Romano V. A. Orru. "Metal-free one-pot α-carboxylation of primary alcohols." Organic & Biomolecular Chemistry 14, no. 41 (2016): 9716–19. http://dx.doi.org/10.1039/c6ob01813k.

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14

Yin, Guodong, Junrui Ma, Houqiang Shi, and Qing Tao. "Facile One-Pot Procedure for the Synthesis of 2-Aminothiazole Derivatives." HETEROCYCLES 85, no. 8 (2012): 1941. http://dx.doi.org/10.3987/com-12-12510.

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15

Michel, Patrick, and André Rassat. "A one-pot procedure for the synthesis of iodoalkynes from aldehydes." Tetrahedron Letters 40, no. 49 (December 1999): 8579–81. http://dx.doi.org/10.1016/s0040-4039(99)01831-6.

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16

Pchalek, Karin, Ashley W. Jones, Monique M. T. Wekking, and David StC Black. "Synthesis of activated 3-substituted indoles: an optimised one-pot procedure." Tetrahedron 61, no. 1 (January 2005): 77–82. http://dx.doi.org/10.1016/j.tet.2004.10.060.

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17

Jedlovská, Eva, and Ján Leško. "A Simple One-Pot Procedure for the Synthesis of 1,3,4-Oxadiazoles." Synthetic Communications 24, no. 13 (July 1994): 1879–85. http://dx.doi.org/10.1080/00397919408010196.

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18

Suzuki, Keisuke, and Tomoichi Shionhara. "Facile One-Pot Procedure for Et3Al-Promoted Asymmetric Pinacol-Type Rearrangement." Synthesis, no. 1 (2003): 0141–46. http://dx.doi.org/10.1055/s-2003-36266.

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19

Sharghi, Hashem, Omid Asemani, and Reza Khalifeh. "New One‐Pot Procedure for the Synthesis of 2‐Substituted Benzimidazoles." Synthetic Communications 38, no. 7 (March 1, 2008): 1128–36. http://dx.doi.org/10.1080/00397910701863657.

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20

Kato, Hirohisa, Ken Ohmori, and Keisuke Suzuki. "Convenient Procedure for One-pot Conversion of Azides to N-Monomethylamines." Synlett 2001, Special Issue (2001): 1003–5. http://dx.doi.org/10.1055/s-2001-14646.

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21

Takahashi, Tamotsu, Baojian Shen, Kiyohiko Nakajima, and Zhenfeng Xi. "ChemInform Abstract: A Convenient One-Pot Procedure to Arylcyclobutenes from Arylacetylenes." ChemInform 31, no. 12 (June 9, 2010): no. http://dx.doi.org/10.1002/chin.200012100.

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22

Severin, Rene, Jessica Reimer, and Sven Doye. "ChemInform Abstract: One-Pot Procedure for the Synthesis of Unsymmetrical Diarylalkynes." ChemInform 41, no. 39 (September 2, 2010): no. http://dx.doi.org/10.1002/chin.201039104.

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23

Nichifor, Marieta, Magdalena Cristina Stanciu, and Bogdan C. Simionescu. "New cationic hydrophilic and amphiphilic polysaccharides synthesized by one pot procedure." Carbohydrate Polymers 82, no. 3 (October 2010): 965–75. http://dx.doi.org/10.1016/j.carbpol.2010.06.027.

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24

Berényi, Sándor, Csaba Csutorás, Susanna Gyulai, and Sándor Makleit. "A SIMPLE, ONE-POT PROCEDURE FOR THE PREPARATION OF DOPAMINERGIC ALKYLTHIOAPOMORPHINES." Organic Preparations and Procedures International 30, no. 1 (February 1998): 100–103. http://dx.doi.org/10.1080/00304949809355267.

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25

Chawla, H. M., and Anuradha Santra. "CONVENIENT ONE POT PROCEDURE FOR SYNTHESIS OF FORMYLATED CALIX[n]ARENES." Synthetic Communications 31, no. 17 (January 1, 2001): 2605–11. http://dx.doi.org/10.1081/scc-100105385.

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26

Samet, Alexander V., Daniel J. Coughlin, A. C. Buchanan, and Andrei A. Gakh. "AN IMPROVED “ONE-POT” PROCEDURE FOR SYNTHESIS OF FLUORINATED DL-PHENYLALANINES." Synthetic Communications 32, no. 6 (January 1, 2002): 941–46. http://dx.doi.org/10.1081/scc-120002709.

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27

Wünsch, Bernhard, Torsten Schläger, Christoph Oberdorf, and Bastian Tewes. "Novel, One-Pot Procedure for the Synthesis of 2-Arylethanol Derivatives." Synthesis 2008, no. 11 (June 2008): 1793–97. http://dx.doi.org/10.1055/s-2008-1067021.

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28

Tanaka, Kiyoshi, Kenji Otsubo, and Kaoru Fuji. "One-Pot Procedure for Producing Allene Carboxylic Esters from BHT Esters." Synlett 1995, no. 09 (September 1995): 933–34. http://dx.doi.org/10.1055/s-1995-5140.

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29

Knol, Joop, and Ben L. Feringa. "One-Pot Procedure for the Synthesis of N-Fumaroyl-2-Oxazolidinones." Synlett 1995, no. 10 (October 1995): 1025–26. http://dx.doi.org/10.1055/s-1995-5171.

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30

Urones, Julio G., Isidro S. Marcos, Narciso M. Garrido, P. Basabe, Sonia G. San Feliciano, Raquel Coca, and David Díez. "Four Chiral Centers in a One Pot Procedure. Analogues of Isosorbide." Synlett 1998, no. 12 (December 1998): 1364–65. http://dx.doi.org/10.1055/s-1998-1957.

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31

Nose, Masatoshi, and Hitomi Suzuki. "Convenient One-pot Procedure for Converting Aryl Sulfides to Nitroaryl Sulfones." Synthesis 2002, no. 08 (2002): 1065–71. http://dx.doi.org/10.1055/s-2002-31950.

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32

Samanta, Debabrata, Anup Rana, Jan W. Bats, and Michael Schmittel. "A one-pot multistep cyclization yielding thiadiazoloimidazole derivatives." Beilstein Journal of Organic Chemistry 10 (December 15, 2014): 2989–96. http://dx.doi.org/10.3762/bjoc.10.317.

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A versatile synthetic procedure is described to prepare the benzimidazole-fused 1,2,4-thiadiazoles 2a–c via a methanesulfonyl chloride initiated multistep cyclization involving the intramolecular reaction of an in-situ generated carbodiimide with a thiourea unit. The structure of the intricate heterocycle 2a was confirmed by single-crystal X-ray analysis and its mechanism of formation supported by DFT computations.

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33

Nguyen, Quoc Vuong, Phuong Diep Thi Lan, Hang Pham Thi, Van Chien Vu, Tuan Nguyen Le, Van Minh Chau, and Van Cuong Pham. "Facile, Protection-Free, One-Pot Synthesis of Aureusidin." Natural Product Communications 9, no. 11 (November 2014): 1934578X1400901. http://dx.doi.org/10.1177/1934578x1400901108.

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A new, reliable, and convenient protection-free one-pot method for the synthesis of aureusidin (1) is described. The present synthetic approach involves the condensation of 4,6-dihydroxybenzofuranone with 3,4-dihydroxybenzaldehyde in the presence of concentrated HCl to afford aureusidin (1) in good yield with high purity. This procedure offers a short and simple route for the preparation of aureusidin (1), a bioactive natural product from several vegetal species, as well as for synthesis of other aurones.

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34

Radtke, M., Caroline Dudley, Jacob O’Leary, and Tristan Lambert. "A Scalable, One-Pot Synthesis of 1,2,3,4,5-Pentacarbomethoxycyclopentadiene." Synthesis 51, no. 05 (January 22, 2019): 1135–38. http://dx.doi.org/10.1055/s-0037-1611650.

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1,2,3,4,5-Pentacarbomethoxycyclopentadiene (PCCP) is a strong organic acid and a precursor to useful organocatalysts, including chiral Brønsted acids and silicon-based Lewis acids. The synthetic route to PCCP, first reported in 1942, is inconvenient for a number of reasons. The two-step synthesis requires the purification of intermediates from intractable side-products, high reaction temperatures, and extensive labor (3 days). We have developed an improved procedure that delivers PCCP efficiently in 24 hours in one pot at ambient temperature and without isolation.

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35

Thakare, Manoj P., Rahimullah Shaikh, and Dipak Tayade. "Silica gel-promoted new one-pot procedure for the synthesis of 1,3-oxathiolan-5-one." Journal of Sulfur Chemistry 38, no. 5 (April 12, 2017): 465–74. http://dx.doi.org/10.1080/17415993.2017.1313256.

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36

Katritzky, Alan R., Geeta Meher, and Tamari Narindoshvili. "Convenient one-pot synthesis of 5-(substituted amino)-1,2,3,4-thiatriazoles." Collection of Czechoslovak Chemical Communications 74, no. 7-8 (2009): 1061–68. http://dx.doi.org/10.1135/cccc2009015.

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37

Lu, Shaonan, Yingfu Lin, Hongban Zhong, Kang Zhao, and Jianhui Huang. "A practical one-pot procedure for the synthesis of N–H isoquinolones." Tetrahedron Letters 54, no. 15 (April 2013): 2001–5. http://dx.doi.org/10.1016/j.tetlet.2013.02.003.

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38

Pasko, Cody M., Amila A. Dissanayake, Brennan S. Billow, and Aaron L. Odom. "One-pot synthesis of pyrroles using a titanium-catalyzed multicomponent coupling procedure." Tetrahedron 72, no. 9 (March 2016): 1168–76. http://dx.doi.org/10.1016/j.tet.2016.01.002.

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39

Hwang, Dah-Ren, Norman R. Simpson, Julie Montoya, J. John Mann, and Marc Laruelle. "An improved one-pot procedure for the preparation of [11C-carbonyl]-WAY100635." Nuclear Medicine and Biology 26, no. 7 (October 1999): 815–19. http://dx.doi.org/10.1016/s0969-8051(99)00056-6.

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40

Astleford, Bret A., Gerald L. Goe, James G. Keay, and Eric F. V. Scriven. "Synthesis of 1-alkyl-1,2,4-triazoles: a new one-pot regiospecific procedure." Journal of Organic Chemistry 54, no. 3 (February 1989): 731–32. http://dx.doi.org/10.1021/jo00264a048.

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41

Hughes, Thomas, and Andrew Korich. "A Facile, One-Pot Procedure for Forming Diarylimines from Nitroarenes and Benzaldehydes." Synlett 2007, no. 16 (October 2007): 2602–4. http://dx.doi.org/10.1055/s-2007-986668.

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42

Cardinale, Jens, and Johannes Ermert. "ChemInform Abstract: Simplified Synthesis of Aryliodonium Ylides by a One-Pot Procedure." ChemInform 44, no. 31 (July 11, 2013): no. http://dx.doi.org/10.1002/chin.201331057.

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43

Wu, Jishan, Chunyan Chi, Xianhong Wang, Ji Li, Xiaojiang Zhao, and Fosong Wang. "ChemInform Abstract: A One-Pot Procedure to Prepare S-Protected 4-Iodothiophenols." ChemInform 32, no. 8 (February 20, 2001): no. http://dx.doi.org/10.1002/chin.200108121.

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44

Zheng, Lianyou, Jinbao Xiang, and Xu Bai. "A one-pot procedure for ring enlargement of α-chloromethylN-containing heterocycles." Journal of Heterocyclic Chemistry 43, no. 2 (March 2006): 321–24. http://dx.doi.org/10.1002/jhet.5570430211.

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45

JANG, W. B., W. S. SHIN, K. LEE, and D. Y. OH. "ChemInform Abstract: Synthesis of β-Amino Phosphonates (III) in One-Pot Procedure." ChemInform 29, no. 8 (June 23, 2010): no. http://dx.doi.org/10.1002/chin.199808149.

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46

Siebeneicher, Holger, Igor Bytschkov, and Sven Doye. "A Flexible and Catalytic One-Pot Procedure for the Synthesis of Indoles." Angewandte Chemie International Edition 42, no. 26 (July 7, 2003): 3042–44. http://dx.doi.org/10.1002/anie.200351345.

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47

Felicetti, Tommaso, Maria Sole Burali, Chin Piaw Gwee, Kitti Wing Ki Chan, Sylvie Alonso, Serena Massari, Stefano Sabatini, et al. "Sustainable, three-component, one-pot procedure to obtain active anti-flavivirus agents." European Journal of Medicinal Chemistry 210 (January 2021): 112992. http://dx.doi.org/10.1016/j.ejmech.2020.112992.

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48

Müller, Stephan, Bernd Liepold, Gerald J. Roth, and Hans Jürgen Bestmann. "An Improved One-pot Procedure for the Synthesis of Alkynes from Aldehydes." Synlett 1996, no. 06 (June 1996): 521–22. http://dx.doi.org/10.1055/s-1996-5474.

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49

Li, Yu-Ling, Kai Wang, Bo Zhao, Qiu-Shi Jiang, Bai-Xiang Du, and Cai-Fa Chen. "One-pot, three-component, green procedure for efficient synthesis of allomaltol derivatives." Research on Chemical Intermediates 41, no. 8 (April 3, 2014): 5149–58. http://dx.doi.org/10.1007/s11164-014-1618-5.

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50

Lekar, Anna V., Sergey N. Borisenko, Elena V. Vetrova, Elena V. Maksimenko, Salima S. Khizrieva, Nikolai I. Borisenko, and Vladimir I. Minkin. "New fast “One-pot” Technique for the Production of Glycyrrhetinic Acid from the Roots of licorice (Glycyrrhiza glabra)." Natural Product Communications 13, no. 7 (July 2018): 1934578X1801300. http://dx.doi.org/10.1177/1934578x1801300709.

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The aim of this work was to develop and study a fast “one-pot” procedure for the production of glycyrrhetinic acid (GLA) from the roots of licorice ( Glycyrrhiza glabra L.) using subcritical water (SBW). Technique requires no use expensive and toxic organic solvents. For the first time the new method was used for the production of glycyrrhetinic acid (aglycone of glycyrrhizic acid) by “one-pot” technique. HPLC was used to determine the quantitative compositions of the obtained products. It has been shown that variation of only one parameter of the process (temperature) allows alteration of composition of the products obtained by new “one-pot” technique. The “one-pot” procedure developed for the production of GLA in SBW is faster (12 folds) than conventional methods that use expensive and toxic organic solvents. The proposed procedure has the excellent potential for the future development of the fast and low cost technologies for the production of GLA and its derivatives in the pharmaceutical, food and cosmetic industries.

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