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Journal articles on the topic 'Total S'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Izquierdo, Paula. "A. S. Byatt: una narradora total." Arbor 185, A1 (2009): 128–34. http://dx.doi.org/10.3989/arbor.2009.ia1.796.

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2

Jung*[], M. "Total Synthesis of (S,S)-Isodityrosine[]." Tetrahedron 53, no. 26 (1997): 8815–24. http://dx.doi.org/10.1016/s0040-4020(97)00570-x.

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3

Jung, Michael E., and Laurie S. Starkey. "Total synthesis of (S,S)-isodityrosine." Tetrahedron 53, no. 26 (1997): 8815–24. http://dx.doi.org/10.1016/s0040-4020(97)90393-8.

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4

Semenenko, Viacheslav, and Andrii Ivashenko. "Russia`s Total War." National security and the future 23, no. 2 (2022): 53–87. http://dx.doi.org/10.37458/nstf.23.2.2.

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The article examines Russia's political goals and military scenarios for Ukraine, as well as options for supporting Ukraine that are available to the United States, its allies and partners in the event of an invasion. New developments and information need further analysis to better understand Russia's intentions and consequences.

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5

Heinrich, Almut. "ESPR´s Total Environment." Environmental Science and Pollution Research - International 14, no. 2 (2007): 140. http://dx.doi.org/10.1065/espr2007.03.396.

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6

Hollert, Henner, Markus Hecker, Christian E. W. Steinberg, and Alvin L. Young. "ESPR´s Total Environment." Environmental Science and Pollution Research 14, S1 (2007): 1–2. http://dx.doi.org/10.1065/espr2007.04.405.

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7

Chinta, Ramakoteswara Rao, V. Harikrishna, Vijaya Kumar Tulam, Naveen Kumar Bejjanki, Prathama S. Mainkar, and P. K. Dubey. "Total Synthesis of S (+)-Curcuphenol, S (+)-Curcuquinone and S (+)-Curcuhydroquinone." Asian Journal of Chemistry 28, no. 4 (2016): 771–78. http://dx.doi.org/10.14233/ajchem.2016.19475.

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8

Pohmakotr, Manat, Patoomratana Tuchinda, Pornchai Premkaisorn, Attasit Limpongpan, and Vichai Reutrakul. "Total Synthesis of (S)-(+)-Melodorinol and (S)-(+)-Acetylmelodorinol." HETEROCYCLES 51, no. 4 (1999): 795. http://dx.doi.org/10.3987/com-98-8449.

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9

Vo, Quan V., Craige Trenerry, Simone Rochfort, and Andrew B. Hughes. "A total synthesis of ( R , S ) S -glucoraphanin." Tetrahedron 69, no. 41 (2013): 8731–37. http://dx.doi.org/10.1016/j.tet.2013.07.097.

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10

JUNG, M. E., and L. S. STARKEY. "ChemInform Abstract: Total Synthesis of (S,S)-Isodityrosine." ChemInform 28, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.199744215.

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11

Sevindik, Emre, İsmail Gübeş, Zehra Tuğba Murathan, and Gülendam Tümen. "Determination of total phenolic content, total flavonoid content and total antioxidant capacity in some endemic Sideritis L. (Lamiaceae) species grown in Turkey." European Journal of Biological Research 11, no. 2 (2021): 260–66. https://doi.org/10.5281/zenodo.4660074.

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In this study, total phenolic, total flavonoid and antioxidant activities of the some endemic species <em>Sideritis rubriflora</em> Hub.-Mor.<em>, Sideritis libanotica</em> Labill.<em> </em>subsp<em>. violascens</em> (P.H.Davis) P.H.Davis<em>, Sideritis erythrantha</em> Boıss. Et Heldr. Apus Bentham<em> </em>var. <em>cedretorum</em> P.H.Davis<em>, Sideritis congesta</em> P. H. Davis Et Hub.-Mor.<em>, Sideritis brevidens</em> P.H.Davis<em> </em>and<em> Sideritis vuralii</em> H. Duman Et Başer, which were collected from Anamur district of Mersin province in Turkey, were analyzed. Total phenolic

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12

Berberich, Stephen M., Robert J. Cherney, John Colucci, et al. "Total synthesis of (+)-ambruticin S." Tetrahedron 59, no. 35 (2003): 6819–32. http://dx.doi.org/10.1016/s0040-4020(03)00370-3.

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13

Kirkland, Thomas A., John Colucci, Leo S. Geraci, et al. "Total Synthesis of (+)-Ambruticin S." Journal of the American Chemical Society 123, no. 49 (2001): 12432–33. http://dx.doi.org/10.1021/ja011867f.

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14

Patel, Jignesh, Nadia Pelloux-Léon, Frédéric Minassian, and Yannick Vallée. "Total synthesis of (S)-(−)-cyclooroidin." Tetrahedron Letters 47, no. 31 (2006): 5561–63. http://dx.doi.org/10.1016/j.tetlet.2006.05.130.

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15

Fujiwara, Kenshu, Takaya Itagaki, Yoshihiko Kondo, Uichi Akiba, and Tetsuo Tokiwano. "Total synthesis of selaginellin S." Tetrahedron Letters 61, no. 25 (2020): 152031. http://dx.doi.org/10.1016/j.tetlet.2020.152031.

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16

Saeed, Muhammad, Muhammad Abbas, Khalid Mohammad Khan, and Wolfgang Voelter. "Total Synthesis of S-(+)-Argentilactone." Zeitschrift für Naturforschung B 56, no. 3 (2001): 325–28. http://dx.doi.org/10.1515/znb-2001-0318.

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Abstract Asymmetrie Total Synthesis Asymmetrie total synthesis of S-(+)-argentilactone (2) was accomplished, using methyl-a-D-glucopyranoside (3) as carbohydrate template. Benzylidene acetal 5 was hydrolysed with tBuOOH/AlCl3 and further manipulated to produce the aldehyde 10. A Wittig reaction and subsequent oxidation of the anomeric position yielded the target argentilactone.

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17

Heemstra, Jennifer M., Sean A. Kerrigan, Daniel R. Doerge, William G. Helferich, and William A. Boulanger. "Total Synthesis of (S)-Equol." Organic Letters 8, no. 24 (2006): 5441–43. http://dx.doi.org/10.1021/ol0620444.

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18

Heemstra, Jennifer M., Sean A. Kerrigan, Daniel R. Doerge, and William G. Helferich, and Willia m A. Boul. "Total Synthesis of (S)-Equol." Organic Letters 9, no. 2 (2007): 379. http://dx.doi.org/10.1021/ol062772r.

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19

Shimada, Naoaki, Yuzo Abe, Satoshi Yokoshima, and Tohru Fukuyama. "Total Synthesis of (−)-Lycoposerramine-S." Angewandte Chemie 124, no. 47 (2012): 11994–96. http://dx.doi.org/10.1002/ange.201206863.

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20

Ichikawa, Yoshiyasu, Keiko Hirata, Masayoshi Ohbayashi, and Minoru Isobe. "Total Synthesis of (+)-Blasticidin S." Chemistry - A European Journal 10, no. 13 (2004): 3241–51. http://dx.doi.org/10.1002/chem.200305358.

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21

Shimada, Naoaki, Yuzo Abe, Satoshi Yokoshima, and Tohru Fukuyama. "Total Synthesis of (−)-Lycoposerramine-S." Angewandte Chemie International Edition 51, no. 47 (2012): 11824–26. http://dx.doi.org/10.1002/anie.201206863.

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22

Farahmand, Nasser Fegh-hi. "Total Business Management." Greener Journal of Economics and Accountancy 2, no. 1 (2012): 1–7. https://doi.org/10.5281/zenodo.3466727.

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This paper describes the corporate-wide approach to Total Business Management (TBM) at organizations. TBM, referring to the internal systematic approach of the organization’s management and leadership to strive for business performance excellence, and Total Business Policy (TBP) referring to all those measures through which one creates and strengthens confidence and trust in outsiders, especially customers, towards the organization’s abilities and products. Naturally, TBP is a part of TBM. The paper reviews the strategy implementation, strategic control, business metrics, business

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23

Yang, Yushe, Liqiang Fu, and Chenyu Ling. "Total Synthesis of (S)-(-)-Stepholidine Using (S)-tert-Butanesulfinylimine." HETEROCYCLES 81, no. 11 (2010): 2581. http://dx.doi.org/10.3987/com-10-12056.

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24

Huang, Zheng, Xiang Ji, and Jean-Philip Lumb. "Total Synthesis of (S,S)-Tetramethylmagnolamine via Aerobic Desymmetrization." Organic Letters 21, no. 22 (2019): 9194–97. http://dx.doi.org/10.1021/acs.orglett.9b03559.

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25

Raj, Ajay, and Tibor Macko. "On manifolds homotopy equivalent to the total spaces of $S^7$-bundles over $S^8$." Archivum Mathematicum, no. 3 (2024): 125–34. http://dx.doi.org/10.5817/am2024-3-125.

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26

Masaki, Yukio, Toshihiro Imaeda, Hirohisa Oda, Akichika Itoh, and Motoo Shiro. "Total Synthesis of (+)-Asperlin Starting with (S,S)-Tartaric Acid." Chemistry Letters 21, no. 7 (1992): 1209–12. http://dx.doi.org/10.1246/cl.1992.1209.

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27

Mallula, Venkata Satyanarayana, Batthula Srinivas, and Palakodety Radha Krishna. "First total synthesis of (6S,1′S,2′S)-hydroxypestalotin." Tetrahedron Letters 56, no. 32 (2015): 4711–13. http://dx.doi.org/10.1016/j.tetlet.2015.06.009.

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28

Sander, Hannah, Samantha Wallace, Rachel Plouse, Shuchita Tiwari, and Aldrin V. Gomes. "Ponceau S waste: Ponceau S staining for total protein normalization." Analytical Biochemistry 575 (June 2019): 44–53. http://dx.doi.org/10.1016/j.ab.2019.03.010.

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29

ONO, Machiko, Yuuko OGURA, Kazumi HATOGAI, and Hiroyuki AKITA. "Total Synthesis of (S)-(+)-Curcudiol, and (S)-(+)-and (R)-(-)-Curcuphenol." CHEMICAL & PHARMACEUTICAL BULLETIN 49, no. 12 (2001): 1581–85. http://dx.doi.org/10.1248/cpb.49.1581.

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30

Pohmakotr, Manat, Patoomratana Tuchinda, Pornchai Premkaisorn, Attasit Limpongpan, and Vichai Reutrakul. "ChemInform Abstract: Total Synthesis of (S)-(+)-Melodorinol and (S)-(+)-Acetylmelodorinol." ChemInform 30, no. 30 (2010): no. http://dx.doi.org/10.1002/chin.199930236.

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31

Sandvik, A. K., and T. B. Halvorsen. "Barrett??s Esophagus after Total Gastrectomy." Journal of Clinical Gastroenterology 10, no. 5 (1988): 587–88. http://dx.doi.org/10.1097/00004836-198810000-00023.

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32

Kaseda, Takehiko, Toyohiko Kikuchi, and Chihiro Kibayashi. "Enantioselective total synthesis of (+)-(S)-dihydroperiphylline." Tetrahedron Letters 30, no. 34 (1989): 4539–42. http://dx.doi.org/10.1016/s0040-4039(01)80739-5.

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33

Kim, Sun Joo, Tae Hong Jeon, Im Sook Min, In Su Kim, and Young Hoon Jung. "Asymmetric total synthesis of (S)-dapoxetine." Tetrahedron Letters 53, no. 28 (2012): 3680–82. http://dx.doi.org/10.1016/j.tetlet.2012.05.037.

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34

Bono, James V. "S-ROM modular total hip replacement." Operative Techniques in Orthopaedics 11, no. 4 (2001): 279–87. http://dx.doi.org/10.1016/s1048-6666(01)80043-4.

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35

Zhong, Mei, Yunbin Jiang, Yali Chen, Qian Yan, Junxi Liu, and Duolong Di. "Asymmetric total synthesis of (S)-isocorydine." Tetrahedron: Asymmetry 26, no. 20 (2015): 1145–49. http://dx.doi.org/10.1016/j.tetasy.2015.09.008.

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36

Cheng, Jian-Jun, and Yu-She Yang. "Enantioselective Total Synthesis of (−)-(S)-Stepholidine." Journal of Organic Chemistry 74, no. 23 (2009): 9225–28. http://dx.doi.org/10.1021/jo9020826.

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37

Liu, Feng, and Chaozhong Li. "Total synthesis of (S)-14-azacamptothecin." Org. Biomol. Chem. 12, no. 4 (2014): 637–42. http://dx.doi.org/10.1039/c3ob41883a.

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38

Liu, Zhu-Jin, Ren-Rong Lu, Qi Chen, and Hai Hong. "A total synthesis of (S)-(+)-ipalbidine." Acta Chimica Sinica 3, no. 3 (1985): 262–65. http://dx.doi.org/10.1002/cjoc.19850030312.

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39

Shimada, Naoaki, Yuzo Abe, Satoshi Yokoshima, and Tohru Fukuyama. "Berichtigung: Total Synthesis of (−)-Lycoposerramine-S." Angewandte Chemie 126, no. 34 (2014): 8952. http://dx.doi.org/10.1002/ange.201311008.

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40

Shimada, Naoaki, Yuzo Abe, Satoshi Yokoshima, and Tohru Fukuyama. "Corrigendum: Total Synthesis of (−)-Lycoposerramine-S." Angewandte Chemie International Edition 53, no. 34 (2014): 8808. http://dx.doi.org/10.1002/anie.201311008.

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41

Dr. Adeel Maqbool, Dr Adeel Maqbool, and Siraj Ahmad. "Total Quality Management through Five "S" In Health Care Organizations." International Journal of Scientific Research 3, no. 1 (2012): 232–34. http://dx.doi.org/10.15373/22778179/jan2014/76.

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42

Huisveld, I. A., J. E. H. Hospers, J. C. M. Meijers, A. E. Starkenburg, W. B. M. Erich, and B. N. Bouma. "Oral contraceptives reduce total protein S, but not free protein S." Thrombosis Research 45, no. 1 (1987): 109–14. http://dx.doi.org/10.1016/0049-3848(87)90262-3.

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43

Cheng, Jianjun, Liqiang Fu, Chenyu Ling, and Yushe Yang. "ChemInform Abstract: Total Synthesis of (S)-(-)-Stepholidine Using (S)-tert-Butanesulfinylimine." ChemInform 42, no. 13 (2011): no. http://dx.doi.org/10.1002/chin.201113204.

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44

Gins, Cornelia. "Zahnmedizin total." ZWR - Das Deutsche Zahnärzteblatt 114, no. 11 (2005): 491. http://dx.doi.org/10.1055/s-2005-922464.

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45

Stucker, Fred, and Daniel Daube. "Reflections on Total and Near Total Nasal Reconstruction." Facial Plastic Surgery 10, no. 04 (1994): 374–81. http://dx.doi.org/10.1055/s-2008-1064587.

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46

Just, George, and Zhi Yuan Wang. "Total synthesis of 8(S)-, 9(S)-, 11(S)-, and 12(S)-hydroxyeicosatetraenoic acids (HETE) methyl esters." Journal of Organic Chemistry 51, no. 25 (1986): 4796–802. http://dx.doi.org/10.1021/jo00375a009.

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47

İNCE, Soydan, Sefer GÜNAYDIN, Belgin PETEK BALCI, Birgül BAŞTAN, Nihat ÇEVİK, and Özlem ÇOKAR. "Wernicke?s Encephalopathy Secondary to Prolonged Total Parenteral Nutrition: Case Report." Turkiye Klinikleri Journal of Neurology 10, no. 2 (2015): 65–68. http://dx.doi.org/10.5336/neuro.2014-40125.

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48

Kobayashi, Susumu, Motoko Oshida, Misaki Ono, and Atsuo Nakazaki. "Total Synthesis of (+)-Cacospongionolide B." HETEROCYCLES 80, no. 1 (2010): 313. http://dx.doi.org/10.3987/com-09-s(s)17.

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49

Abe, Hitoshi, Daichi Ogura, and Yoshikazu Horino. "Total Synthesis of Oenothein C." HETEROCYCLES 95, no. 1 (2017): 131. http://dx.doi.org/10.3987/com-16-s(s)6.

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50

Inoue, Seiichi, Toshihiko Kaneko, Yuichi Takahashi, Osamu Miyamoto, and Kikumasa Sato. "Stereoselective total synthesis of (S)-(–)-dolichol-20." J. Chem. Soc., Chem. Commun., no. 13 (1987): 1036–37. http://dx.doi.org/10.1039/c39870001036.

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