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Journal articles on the topic 'Protecting groups'

Author: Grafiati

Published: 4 June 2021

Last updated: 14 February 2022

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1

Jarowicki, Krzysztof, and Philip Kocienski. "Protecting groups." Contemporary Organic Synthesis 2, no. 5 (1995): 315. http://dx.doi.org/10.1039/co9950200315.

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2

Jarowicki, Krzysztof, and Philip Kocienski. "Protecting groups." Contemporary Organic Synthesis 3, no. 5 (1996): 397. http://dx.doi.org/10.1039/co9960300397.

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3

Jarowicki, Krzysztof, and Philip Kocienski. "Protecting groups." Contemporary Organic Synthesis 4, no. 6 (1997): 454. http://dx.doi.org/10.1039/co9970400454.

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4

White, J. D. "Protecting Groups." Synthesis 1994, no. 11 (1994): 1195–96. http://dx.doi.org/10.1055/s-1994-25671.

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5

Jarowicki, Krzysztof, and Philip Kocienski. "Protecting groups." Journal of the Chemical Society, Perkin Transactions 1, no. 16 (2000): 2495–527. http://dx.doi.org/10.1039/b003410j.

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6

Jarowicki, Krzysztof, and Philip Kocienski. "Protecting groups." Journal of the Chemical Society, Perkin Transactions 1, no. 23 (1998): 4005. http://dx.doi.org/10.1039/a803688h.

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7

Jarowicki, Krzysztof, and Philip Kocienski. "Protecting groups." Journal of the Chemical Society, Perkin Transactions 1, no. 18 (2001): 2109–35. http://dx.doi.org/10.1039/b103282h.

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8

Jarowicki, Krzysztof, and Philip Kocieński. "Protecting groups." Journal of the Chemical Society, Perkin Transactions 1, no. 12 (1999): 1589–616. http://dx.doi.org/10.1039/a902440i.

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9

Sarmah, Manash P., and Mysore S. Shashidhar. "Sulfonate protecting groups." Carbohydrate Research 338, no. 9 (2003): 999–1001. http://dx.doi.org/10.1016/s0008-6215(03)00052-1.

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10

Walker, Linda. "Protecting vulnerable groups." Dental Nursing 15, no. 2 (2019): 90–93. http://dx.doi.org/10.12968/denn.2019.15.2.90.

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11

Simpson, Maggie. "Protecting vulnerable groups." Early Years Educator 13, no. 9 (2012): 7. http://dx.doi.org/10.12968/eyed.2012.13.9.7.

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12

Balduzzi, Sonya, and Michael A. Brook. "Alkoxyallylsilanes: Functional Protecting Groups." Tetrahedron 56, no. 12 (2000): 1617–22. http://dx.doi.org/10.1016/s0040-4020(99)01062-5.

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13

Isidro-Llobet, Albert, Mercedes Álvarez, and Fernando Albericio. "Amino Acid-Protecting Groups." Chemical Reviews 109, no. 6 (2009): 2455–504. http://dx.doi.org/10.1021/cr800323s.

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14

Jarowicki, Krzysztof, and Philip Kocienski. "ChemInform Abstract: Protecting Groups." ChemInform 31, no. 50 (2000): no. http://dx.doi.org/10.1002/chin.200050241.

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15

JAROWICKI, K., and P. KOCIENSKI. "ChemInform Abstract: Protecting Groups." ChemInform 27, no. 27 (2010): no. http://dx.doi.org/10.1002/chin.199627319.

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16

JAROWICKI, K., and P. KOCIENSKI. "ChemInform Abstract: Protecting Groups." ChemInform 28, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199708252.

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17

JAROWICKI, K., and P. KOCIENSKI. "ChemInform Abstract: Protecting Groups." ChemInform 29, no. 15 (2010): no. http://dx.doi.org/10.1002/chin.199815279.

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18

Jarowicki, Krzysztof, and Philip Kocienski. "ChemInform Abstract: Protecting Groups." ChemInform 30, no. 14 (2010): no. http://dx.doi.org/10.1002/chin.199914300.

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19

Jarowicki, Krzysztof, and Philip Kocienski. "ChemInform Abstract: Protecting Groups." ChemInform 30, no. 41 (2010): no. http://dx.doi.org/10.1002/chin.199941287.

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20

Jarowicki, Krzysztof, and Philip Kocienski. "ChemInform Abstract: Protecting Groups." ChemInform 33, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.200207262.

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21

Pirrung, Michael C., Lara Fallon, Jin Zhu, and Yong Rok Lee. "Photochemically Removable Silyl Protecting Groups." Journal of the American Chemical Society 123, no. 16 (2001): 3638–43. http://dx.doi.org/10.1021/ja002370t.

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22

Pétursson, Sigthór. "Protecting Groups in Carbohydrate Chemistry." Journal of Chemical Education 74, no. 11 (1997): 1297. http://dx.doi.org/10.1021/ed074p1297.

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23

Reinerth, William A., and James M. Tour. "Protecting Groups for Organoselenium Compounds." Journal of Organic Chemistry 63, no. 7 (1998): 2397–400. http://dx.doi.org/10.1021/jo972144a.

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24

Pirrung, Michael C., and Yong Rok Lee. "Photochemically-removable silyl protecting groups." Journal of Organic Chemistry 58, no. 25 (1993): 6961–63. http://dx.doi.org/10.1021/jo00077a010.

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25

Bochet, Christian G. "Orthogonal Photolysis of Protecting Groups." Angewandte Chemie International Edition 40, no. 11 (2001): 2071–73. http://dx.doi.org/10.1002/1521-3773(20010601)40:11<2071::aid-anie2071>3.0.co;2-9.

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26

HAUSMAN, DANIEL. "PROTECTING GROUPS FROM GENETIC RESEARCH." Bioethics 22, no. 3 (2008): 157–65. http://dx.doi.org/10.1111/j.1467-8519.2007.00625.x.

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27

Hurevich, Mattan, Mamidi Samarasimhareddy, Israel Alshanski, and Evgeniy Mervinetsky. "Photodeprotection of up to Eight Photolabile Protecting Groups from a Single Glycan." Synlett 29, no. 07 (2018): 880–84. http://dx.doi.org/10.1055/s-0036-1591915.

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Abstract:

Permanent protecting groups are essential for oligosaccharide synthesis. However, the removal of the traditionally used protecting groups is not trivial and demands considerable expertise. Using photolabile protecting groups as permanent protection for glycan can overcome many limitations associated with the traditional oligosaccharide synthesis approach. It is demonstrated here that up to eight photolabile protecting groups can be readily removed from a single glycan using a benchtop LED setup that is very easy to operate. This report suggests that further development of the strategy will off

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28

Miyagawa, Atsushi. "Stereoselective Glycosylation by Ether Protecting Groups." Trends in Glycoscience and Glycotechnology 31, no. 182 (2019): E109—E110. http://dx.doi.org/10.4052/tigg.1964.6e.

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29

Miyagawa, Atsushi. "Stereoselective Glycosylation by Ether Protecting Groups." Trends in Glycoscience and Glycotechnology 31, no. 182 (2019): J109—J110. http://dx.doi.org/10.4052/tigg.1964.6j.

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30

Ellervik, Ulf. "9-Anthraldehyde acetals as protecting groups." Tetrahedron Letters 44, no. 11 (2003): 2279–81. http://dx.doi.org/10.1016/s0040-4039(03)00276-4.

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31

Kieburg, Christoffer, and Thisbe K. Lindhorst. "Glycodendrimer synthesis without using protecting groups." Tetrahedron Letters 38, no. 22 (1997): 3885–88. http://dx.doi.org/10.1016/s0040-4039(97)00760-0.

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32

Kim, C. U., and P. F. Misco. "New oxidatively removable carboxy protecting groups." Tetrahedron Letters 26, no. 17 (1985): 2027–30. http://dx.doi.org/10.1016/s0040-4039(00)94770-1.

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33

Aly, Mohamed R. E., and Richard R. Schmidt. "New Diacylamino Protecting Groups for Glucosamine." European Journal of Organic Chemistry 2005, no. 20 (2005): 4382–92. http://dx.doi.org/10.1002/ejoc.200500107.

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34

Wang, Pengfei. "Photolabile Protecting Groups: Structure and Reactivity." Asian Journal of Organic Chemistry 2, no. 6 (2013): 452–64. http://dx.doi.org/10.1002/ajoc.201200197.

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35

Maier, Martin E. "Protecting Groups. By P. J. Kocieński." Advanced Synthesis & Catalysis 346, no. 5 (2004): 583. http://dx.doi.org/10.1002/adsc.200404049.

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36

Doye, Sven. "Protecting Groups. Von Philip J. Kocienski." Chemie in unserer Zeit 40, no. 4 (2006): 268. http://dx.doi.org/10.1002/ciuz.200690058.

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37

Kawano, Y., T. Takada, M. Nakamura, and K. Yamana. "DNA ligation using photoremovable protecting groups." Nucleic Acids Symposium Series 53, no. 1 (2009): 173–74. http://dx.doi.org/10.1093/nass/nrp087.

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38

Montenegro, M. I. "The electrochemical cleavage of protecting groups." Electrochimica Acta 31, no. 6 (1986): 607–20. http://dx.doi.org/10.1016/0013-4686(86)87027-x.

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39

Codée, Jeroen D. C., Asghar Ali, Herman S. Overkleeft, and Gijsbert A. van der Marel. "Novel protecting groups in carbohydrate chemistry." Comptes Rendus Chimie 14, no. 2-3 (2011): 178–93. http://dx.doi.org/10.1016/j.crci.2010.05.010.

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40

Doherty-Kirby, Amanda L., and Gilles A. Lajoie. "ChemInform Abstract: Side-Chain Protecting Groups." ChemInform 32, no. 30 (2010): no. http://dx.doi.org/10.1002/chin.200130247.

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41

Hoffmann, Reinhard W. "ChemInform Abstract: Synthesis Without Protecting Groups." ChemInform 44, no. 16 (2013): no. http://dx.doi.org/10.1002/chin.201316247.

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42

McKay, Laura J., Carl-Johan Carling, and Neil R. Branda. "Improved polyaromatic benzoin photoremovable protecting groups." Journal of Photochemistry and Photobiology A: Chemistry 421 (December 2021): 113530. http://dx.doi.org/10.1016/j.jphotochem.2021.113530.

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43

Singh, Praveen Kumar, Poulomi Majumdar, and Surya Prakash Singh. "Advances in BODIPY photocleavable protecting groups." Coordination Chemistry Reviews 449 (December 2021): 214193. http://dx.doi.org/10.1016/j.ccr.2021.214193.

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44

Pátek, Marcel, and Michal Lebl. ""Safety-Catch" Protecting Groups in Peptide Synthesis." Collection of Czechoslovak Chemical Communications 57, no. 3 (1992): 508–24. http://dx.doi.org/10.1135/cccc19920508.

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Abstract:

A new benzhydryl-type protective groups for amides based on the concept of converting a stable protecting group into a labile one (safety-catch principle) are described. The p-substituted benzhydrylamine derivatives III(a, b), IV(a, b) are shown to be labile toward various acids but in their oxidized state - V(a, b), VI(a, b) exhibit the resistance to conditions commonly used for removal the Boc group. Independent removal of Boc or Fmoc groups, each in the presence of derivative VIa, is demonstrated by a synthesis of Pro-Leu-Gly-NH2. Some mechanistic aspects of deprotection reaction are discus

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45

Ramos-Tomillero, Iván, Lorena Mendive-Tapia, Miriam Góngora-Benítez, Ernesto Nicolás, Judit Tulla-Puche, and Fernando Albericio. "Understanding Acid Lability of Cysteine Protecting Groups." Molecules 18, no. 5 (2013): 5155–62. http://dx.doi.org/10.3390/molecules18055155.

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46

Orain, David, John Ellard, and Mark Bradley. "Protecting Groups in Solid-Phase Organic Synthesis." Journal of Combinatorial Chemistry 4, no. 1 (2002): 1–16. http://dx.doi.org/10.1021/cc0001093.

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47

STINSON, STEPHEN. "Protecting groups: New ways on and off." Chemical & Engineering News 75, no. 17 (1997): 28–29. http://dx.doi.org/10.1021/cen-v075n017.p028.

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48

Malan, Christophe, Christophe Morin, and Gaëtan Preckher. "Two reducible protecting groups for boronic acids." Tetrahedron Letters 37, no. 37 (1996): 6705–8. http://dx.doi.org/10.1016/s0040-4039(96)01468-2.

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49

Roberts, John C., Huai Gao, Ariamala Gopalsamy, Azis Kongsjahju, and Raymond J. Patch. "Neopentyl ester protecting groups for arylsulfonic acids." Tetrahedron Letters 38, no. 3 (1997): 355–58. http://dx.doi.org/10.1016/s0040-4039(96)02302-7.

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50

Bochet, Christian G. "Wavelength-selective cleavage of photolabile protecting groups." Tetrahedron Letters 41, no. 33 (2000): 6341–46. http://dx.doi.org/10.1016/s0040-4039(00)01050-9.

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