Protecting group (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Protecting group" in English language version.

refsWebsite
Global rank English rank
2nd place
2nd place
4th place
4th place
low place
low place
low place
low place
6th place
6th place
3,510th place
2,263rd place
18th place
17th place
11th place
8th place

archive.org

chempep.com

doi.org

  • Michael Schelhaas, Herbert Waldmann: "Schutzgruppenstrategien in der organischen Synthese", in: Angewandte Chemie, 1996, 103, pp. 2194; doi:10.1002/ange.19961081805 (in German).
  • Michael Schelhaas, Herbert Waldmann: "Schutzgruppenstrategien in der organischen Synthese", in: Angewandte Chemie, 1996, 103, pp. 2195–2200; doi:10.1002/ange.19961081805 (in German).
  • Tod K Jones, Robert A. Reamer, Richard Desmond, Sander G. Mills: "Chemistry of tricarbonyl hemiketals and application of Evans technology to the total synthesis of the immunosuppressant (−)-FK-506", in: J. Am. Chem. Soc., 1990, 112, pp. 2998–3017; doi:10.1021/ja00164a023.
  • Dieter Seebach, Hak-Fun Chow, Richard F.W. Jackson, Marius A. Sutter, Suvit Thaisrivongs, Jürg Zimmermann: "(+)-11,11-Di-O-methylelaiophylidene – preparation from elaiophylin and total synthesis from (R)-3-hydroxybutyrate and (S)-malate", in: Liebigs Ann. Chem., 1986, pp. 1281–1308; doi:10.1002/jlac.198619860714.
  • David A. Evans, Stephen W. Kaldor, Todd K. Jones, Jon Clardy, Thomas J. Stout: "Total synthesis of the macrolide antibiotic cytovaricin", in: J. Am. Chem. Soc., 1990, 112, pp. 7001–7031; doi:10.1021/ja00175a038.
  • James A. Marshall, Richard Sedrani: "A convergent, highly stereoselective synthesis of a C-11-C-21 subunit of the macbecins", in: J. Org. Chem., 1991, 56, pp. 5496–5498; doi:10.1021/jo00019a004.
  • James D. White, Motoji Kawasaki: "Total synthesis of (+)-latrunculin A", in: J. Am. Chem. Soc., 1990, 112, pp. 4991–4993; doi:10.1021/ja00168a071.
  • Morris J. Robins, Vicente Samano, Mark D. Johnson: "Nucleic acid-related compounds. 58. Periodinane oxidation, selective primary deprotection, and remarkably stereoselective reduction of tert-butyldimethylsilyl-protected ribonucleosides. Synthesis of 9-(β-D-xylofuranosyl)adenine or 3'-deuterioadenosine from adenosine", in: J. Org. Chem., 1990, 55, pp. 410–412; doi:10.1021/jo00289a004.
  • R. Roger F. Newton, Derek P. Reynolds, Colin F. Webb, Stanley M. Roberts: "A short and efficient total synthesis of (±) prostaglandin D2 methyl ester involving a new method for the cleavage of a dimethyl-t-butylsilyl ether", in: J. Chem. Soc., Perkin Trans. 1, 1981, pp. 2055–2058; doi:10.1039/P19810002055.
  • Kyriacos C. Nicolaou, R. A. Daines, T. K. Chakraborty: "Total synthesis of amphoteronolide B", in: J. Am. Chem. Soc., 1987, 109, pp. 2208–2210; doi:10.1021/ja00241a063.
  • Leo A. Paquette, Annette M. Doherty, Christopher M. Rayner: "Total synthesis of furanocembranolides. 1. Stereocontrolled preparation of key heterocyclic building blocks and assembly of a complete seco-pseudopterane framework", in: J. Am. Chem. Soc., 1991, 109, pp. 3910–3926; doi:10.1021/ja00036a045.
  • Michel Bessodes, Dimitri Komiotis, Kostas Antonakis: "Rapid and selective detritylation of primary alcohols using formic acid", in: Tetrahedron Lett., 1986, 27, pp. 579–580; doi:10.1016/S0040-4039(00)84045-9.
  • M.L. García, J. Pascual, L. Borràs, J.A. Andreu, E. Fos, D. Mauleón, G. Carganico, F. Arcamone: "Synthesis of new ether glycerophospholipids structurally related to modulator", in: Tetrahedron, 1991, 47, pp. 10023–10034; doi:10.1016/S0040-4020(01)96051-X.
  • Yuji Oikawa, Tadao Yoshioka, Osamu Yonemitsu: "Specific removal of o-methoxybenzyl protection by DDQ oxidation", in: Tetrahedron Lett., 1982, 23, pp. 885–888; doi:10.1016/S0040-4039(00)86974-9.
  • H. Nagaoka, W. Rutsch, G. Schmidt, H. Ito, M.R. Johnson, Y. Kishi: "Total synthesis of rifamycins. 1. Stereocontrolled synthesis of the aliphatic building block", in: J. Am. Chem. Soc., 1980, 102, pp. 7962–7965; doi:10.1021/ja00547a037.
  • W. Clark Still, Dominick Mobilio: "Synthesis of asperdiol", in: J. Org. Chem., 1983, 48, pp. 4785–4786; doi:10.1021/jo00172a070.
  • Masahiro Hirama, Mitsuko Uei: "A chiral total synthesis of compactin", in: J. Am. Chem. Soc., 1982, 104, pp. 4251–4253; doi:10.1021/ja00379a037.
  • W. Clark Still, Shizuaki Murata, Gilbert Revial, Kazuo Yoshihara: "Synthesis of the cytotoxic germacranolide eucannabinolide", in: J. Am. Chem. Soc., 1983, 105, pp. 625–627; doi:10.1021/ja00341a055.
  • Kamaya, Yasushi; T Higuchi (2006). "Metabolism of 3,4-dimethoxycinnamyl alcohol and derivatives by Coriolus versicolor". FEMS Microbiology Letters. 24 (2–3): 225–229. doi:10.1111/j.1574-6968.1984.tb01309.x.
  • Serge David, Annie Thieffry, Alain Veyrières: "A mild procedure for the regiospecific benzylation and allylation of polyhydroxy-compounds via their stannylene derivatives in non-polar solvents", in: J. Chem. Soc., Perkin Trans. 1, 1981, pp. 1796–1801; doi:10.1039/P19810001796.
  • Paul A. Wender, Carlos R. D. Correia: "Intramolecular photoinduced diene-diene cyaloadditions: a selective method for the synthesis of complex eight-membered rings and polyquinanes", in: J. Am. Chem. Soc., 1987, 109, pp. 2523–2525; doi:10.1021/ja00242a053.
  • Karel F. Bernady, M. Brawner Floyd, John F. Poletto, Martin J. Weiss: "Prostaglandins and congeners. 20. Synthesis of prostaglandins via conjugate addition of lithium trans-1-alkenyltrialkylalanate reagents. A novel reagent for conjugate 1,4-additions", in: J. Org. Chem., 1979, 44, pp. 1438–1447; doi:10.1021/jo01323a017.
  • Elias J. Corey, Haruki Niwa, Jochen Knolle: "Total synthesis of (S)-12-hydroxy-5,8,14-cis,-10-trans-eicosatetraenoic acid (Samuelsson's HETE)", in: J. Am. Chem. Soc., 1978, 100, pp. 1942–1943; doi:10.1021/ja00474a058.
  • Elias J. Corey, Mark G. Bock: "Protection of primary hydroxyl groups as methylthiomethyl ethers", in: Tetrahedron Lett., 1975, 16, pp. 3269–3270; doi:10.1016/S0040-4039(00)91422-9.
  • Elias J. Corey, Duy H. Hua, Bai Chuan Pan, Steven P. Seitz: "Total synthesis of aplasmomycin", in: J. Am. Chem. Soc., 1982, 104, pp. 6818–6820; doi:10.1021/ja00388a074.
  • Robert C. Gadwood, Renee M. Lett, Jane E. Wissinger: "Total synthesis of (±)-poitediol and (±)4-epipoitediol", in: J. Am. Chem. Soc., 1984, 106, pp. 3869–3870; doi:10.1021/ja00325a032.
  • Steven D. Burke, Gregory J. Pacofsky: "The ester enolate claisen rearrangement. Total synthesis of (±)-ethisolide", in: Tetrahedron Lett., 1986, 27, pp. 445–448; doi:10.1016/S0040-4039(00)85501-X.
  • Toshiyuki Kan, Masaru Hashimoto, Mitsutoshi Yanagiya, Haruhisa Shirahama: "Effective deprotection of 2-(trimethylsilylethoxy)methylated alcohols (SEM ethers). Synthesis of thyrsiferyl-23 acetate", in: Tetrahedron Lett., 1988, 29, pp. 5417–5418; doi:10.1016/S0040-4039(00)82883-X.
  • Joseph P. Marino, Scott L. Dax: "An efficient desilylation method for the generation of o-quinone methides: application to the synthesis of (+)- and (−)-hexahydrocannabinol", in: J. Org. Chem., 1984, 49, pp. 3671–3672; doi:10.1021/jo00193a051.
  • R.E. Ireland, D.W. Norbeck: "Convergent synthesis of polyether ionophore antibiotics: the synthesis of the monensin bis(tetrahydrofuran) via the Claisen rearrangement of an ester enolate with a β-leaving group", in: J. Am. Chem. Soc., 1985, 107, pp. 3279–3285; doi:10.1021/ja00297a038.
  • András Lipták, János Imre, János Harangi, Pál Nánási, András Neszmélyi: "Chemo-, stereo- and regioselective hydrogenolysis of carbohydrate benzylidene acetals. Synthesis of benzyl ethers of benzyl α-D-, methyl β-D-mannopyranosides and benzyl α-D-rhamnopyranoside by ring cleavage of benzylidene derivatives with the LiAlH4-AlCl3 reagent", in: Tetrahedron, 1982, 38, pp. 3721–3727; doi:10.1016/0040-4020(82)80083-5.
  • James A. Marshall, Joseph D. Trometer, Bruce E. Blough, Thomas D. Crute: "Stereochemistry of SN2' additions to acyclic vinyloxiranes", in J. Org. Chem., 1988, 53, pp. 4274–4282 doi:10.1021/jo00253a020.
  • John O. Osby, Michael G. Martin, Bruce Ganem: An Exceptionally Mild Deprotection of Phthalimides, in: Tetrahedron Lett., 1984, 25, pp. 2093–2096; doi:10.1016/S0040-4039(01)81169-2.
  • Robert M. Williams, Peter J. Sinclair, Dongguan Zhai, Daimo Chen: "Practical asymmetric syntheses of α-amino acids through carbon-carbon bond constructions on electrophilic glycine templates", in: J. Am. Chem. Soc., 1988, 110, p. 1547–1557; doi:10.1021/ja00213a031.
  • Glenn L. Stahl, Roderich Walter, Clarck W. Smith: "General procedure for the synthesis of mono-N-acylated 1,6-diaminohexanes", in: J. Org. Chem., 1978, 43, pp. 2285–2286; doi:10.1021/jo00405a045.
  • Naomi Sakai, Yasufumi Ohfune: "Total synthesis of galantin I. Acid-catalyzed cyclization of galantinic acid", in: J. Am. Chem. Soc., 1992, 114, pp. 998–1010; doi:10.1021/ja00029a031.
  • Moussa, Ziad; D. Romo (2006). "Mild deprotection of primary N-(p-toluenesufonyl) amides with SmI2 following trifluoroacetylation". Synlett. 2006 (19): 3294–3298. doi:10.1055/s-2006-951530.
  • T. Tsunoda, M. Suzuki, R. Noyori: "A facile procedure for acetalization under aprotic conditions", in: Tetrahedron Lett., 1980, 21, pp. 1357–1358; doi:10.1016/S0040-4039(00)74575-8.
  • Juji Yoshimura, Shigeomi Horito, Hiroriobu Hashimoto: "Facile Synthesis of 2,3,4,6-Tetra-O-benzyl-D-glucopyranosylidene Acetals Using Trimethylsilyl Trifluoromethanesulfonate Catalyst", in: Chem. Lett., 1981, 10, pp. 375–376; doi:10.1246/cl.1981.375.
  • Bruce H. Lipshutz, Daniel Pollart, Joseph Monforte, Hiyoshizo Kotsuki: "Pd(II)-catalyzed acetal/ketal hydrolysis/exchange reactions", in: Tetrahedron Lett., 1985, 26, pp. 705–708; doi:10.1016/S0040-4039(00)89114-5.
  • Kwan Soo Kim, Yang Heon Song, Bong Ho Lee, Chi Sun Hahn: "Efficient and selective cleavage of acetals and ketals using ferric chloride adsorbed on silica gel", in: J. Org. Chem., 1986, 51, pp. 404–407; doi:10.1021/jo00353a027.
  • Samuel J. Danishefsky, Nathan B. Mantlo, Dennis S. Yamashita, Gayle. Schulte: "Concise route to the calichemicin-esperamicin series: the crystal structure of an aglycone prototype", in: J. Am. Chem. Soc., 1988, 110, pp. 6890–6891; doi:10.1021/ja00228a051.
  • John N. Haseltine, Maria Paz Cabal, Nathan B. Mantlo, Nobuharu Iwasawa, Dennis S. Yamashita, Robert S. Coleman, Samuel J. Danishefsky, Gayle K. Schulte: "Total synthesis of calicheamicinone: new arrangements for actuation of the reductive cycloaromatization of aglycon congeners", in: J. Am. Chem. Soc., 1991, 113, pp. 3850–3866; doi:10.1021/ja00010a030.
  • Peter Mohr, Nada Waespe-Šarčević, Christoph Tamm, Krystyna Gawronska, Jacek K. Gawronski: "A Study of Stereoselective Hydrolysis of Symmetrical Diesters with Pig Liver Esterase", in: Helv. Chim. Acta, 1983, 66, pp. 2501–2511; doi:10.1002/hlca.19830660815.
  • Théophile Tschamber, Nada Waespe-Šarčević, Christoph Tamm: "Stereocontrolled Synthesis of an Epimer of the C(19)-to-C(27) Segment of Rifamycin S", in: Helv. Chim. Acta, 1986, 69, pp. 621–625; doi:10.1002/hlca.19860690311.
  • Yves Rubin, Carolyn B. Knobler, Francois Diederich: "Precursors to the cyclo[n]carbons: from 3,4-dialkynyl-3-cyclobutene-1,2-diones and 3,4-dialkynyl-3-cyclobutene-1,2-diols to cyclobutenodehydroannulenes and higher oxides of carbon", in: J. Am. Chem. Soc., 1990, 112, pp. 1607–1617; doi:10.1021/ja00160a047.
  • Sunggak Kim, Yong Gil Kim, Deog-il Kim: "A novel method for selective dioxolanation of ketones in the presence of aldehydes", in: Tetrahedron Lett., 1992, 33, pp. 2565–2566; doi:10.1016/S0040-4039(00)92243-3.
  • G. Bauduin, D. Bondon, Y. Pietrasanta, B. Pucci: "Reactions de transcetalisation – II: Influence des facteurs steriques et electroniques sur les energies de cetalisation", in: Tetrahedron, 1978, 34, pp. 3269–3274; doi:10.1016/0040-4020(78)80243-9.
  • John E. McMurry, Stephen J. Isser: "Total synthesis of longifolene", in: J. Am. Chem. Soc., 1972, 94, pp. 7132–7137; doi:10.1021/ja00775a044.
  • M.P. Bosch, M. Pilar Bosch, Francisco Camps, Jose Coll, Angel Guerrero, Toshio Tatsuoka, Jerrold Meinwald: "A stereoselective total synthesis of (±)-muzigadial", in: J. Org. Chem., 1986, 51, pp. 773–784; doi:10.1021/jo00356a002.
  • Ulrich Schmidt, Thomas Beuttler, Albrecht Lieberknecht, Helmut Griesser: "Aminosäuren und peptide – XXXXII. Synthese von Chlamydocin + epi-Chlamydocin", in: Tetrahedron Lett., 1983, 24, pp. 3573–3576; doi:10.1016/S0040-4039(00)88171-X (in German).
  • Elias J. Corey, Plato A. Magriotis: "Total synthesis and absolute configuration of 7,20-diisocyanoadociane", in: J. Am. Chem. Soc., 1987, 109, pp. 287–289; doi:10.1021/ja00235a052.
  • Elias J. Corey, Kyriacos C. Nicolaou, Takeshi Toru: "Total synthesis of (±)-vermiculine", in: J. Am. Chem. Soc., 1975, 97, pp. 2287–2288; doi:10.1021/ja00841a058.
  • Tainejiro Hiyama, Akihiro Kanakura, Hajime Yamamoto, Hitosi Nozaki: "General Route to α,β-unsaturated Aldehydes of Homoterpenoid and terpenoid Structure. Sythesis of JH-II and β-Sinensal", in: Tetrahedron Lett., 1978, 19, pp. 3051–3054; doi:10.1016/S0040-4039(01)94936-6.
  • Romanski, J.; Nowak, P.; Kosinski, K.; Jurczak, J. (September 2012). "High-pressure transesterification of sterically hindered esters". Tetrahedron Lett. 53 (39): 5287–5289. doi:10.1016/j.tetlet.2012.07.094.
  • Ahmed M. Tafesh, Jens Weiguny: "A Review of the Selective Catalytic Reduction of Aromatic Nitro Compounds into Aromatic Amines, Isocyanates, Carbamates, and Ureas Using CO", in: Chem. Rev., 1996, 96, pp. 2035–2052; doi:10.1021/cr950083f.
  • Evan L. Allred, Boyd R. Beck, Kent J. Voorhees: "Formation of carbon-carbon double bonds by the reaction of vicinal dihalides with sodium in ammonia", in: J. Org. Chem., 1974, 39, pp. 1426–1427; doi:10.1021/jo00926a024.
  • Timothy S. Butcher, Feng Zhou, Michael R. Detty: "Debrominations of vic-Dibromides with Diorganotellurides. 1. Stereoselectivity, Relative Rates, and Mechanistic Implications", in: J. Org. Chem., 1998, 63, pp. 169–176; doi:10.1021/jo9713363.
  • C. J. Li, David N. Harpp: "Bis(triphenylstanyl)telluride a mild and selective reagent for telluration and debromination", in: Tetrahedron Lett., 1990, 31, pp. 6291–6293; doi:10.1016/S0040-4039(00)97045-X.
  • Corrado Malanga, Serena Mannucci, Luciano Lardicci: "Carbon-halogen bond activation by nickel catalyst: Synthesis of alkenes, from 1,2-dihalides", in: Tetrahedron, 1998, 54, pp. 1021–1028; doi:10.1016/S0040-4020(97)10203-4.
  • Byung Woo Yoo, Seo Hee Kim, Jun Ho Kim: "A Mild, Efficient, and Selective Debromination of vic-Dibromides to Alkenes with Cp2TiCl2/Ga System", in: Bull. Korean Chem. Soc., 2010, 31, pp. 2757–2758; doi:10.5012/bkcs.2010.31.10.2757.
  • Antonius J. H. Klunder, Jie Zhu, Binne Zwanenburg: "The Concept of Transient Chirality in the Stereoselective Synthesis of Functionalized Cycloalkenes Applying the Retro-Diels-Alder Methodology", in: Chem. Rev., 1999, 99, pp. 1163–1190; doi:10.1021/cr9803840.
  • Hideyuki Tanaka, Takashi Kamikubo, Naoyuki Yoshida, Hideki Sakagami, Takahiko Taniguchi, Kunio Ogasawara: "Enantio- and Diastereocontrolled Synthesis of (−)-Iridolactone and (+)-Pedicularis-lactone", in: Org. Lett., 2001, 3, pp. 679–681; doi:10.1021/ol0070029.
  • Martin Banwell, David Hockless, Bevyn Jarrott, Brian Kelly, Andrew Knill, Robert Longmore, Gregory Simpson: "Chemoenzymatic approaches to the decahydro-as-indacene cores associated with the spinosyn class of insecticide", in: J. Chem. Soc., Perkin Trans. 1, 2000, pp. 3555–3558; doi:10.1039/b006759h.
  • Wenzel E. Davidsohn, Malcolm C. Henry: "Organometallic Acetylenes of the Main Groups III–V", in: Chem. Rev., 1967, 67, pp. 73–106; doi:10.1021/cr60245a003.
  • Barry J. Teobald: "The Nicholas reaction: the use of dicobalt hexacarbonyl-stabilised propargylic cations in synthesis", in: Tetrahedron, 2002, 58, pp. 4133–4170; doi:10.1016/S0040-4020(02)00315-0.
  • Kenneth M. Nicholas, R. Pettit: "An alkyne protection group", in: Tetrahedron Lett., 1971, 37, pp. 3475–3478; doi:10.1016/S0040-4039(01)97209-0.
  • Richard E. Connor, Kenneth M. Nicholas: "Isolation, characterization, and stability of α-[(ethynyl)dicobalt hexacarbonyl] carbonium ions", in: J. Organomet. Chem., 1977, 125, C45–C48; doi:10.1016/S0022-328X(00)89454-1.
  • Rosa F. Lockwood, Kenneth M. Nicholas: "Transition metal-stabilized carbenium ions as synthetic intermediates. I. α-[(alkynyl)dicobalt hexacarbonyl] carbenium ions as propargylating agents", in: Tetrahedron Lett., 1977, pp. 4163–4166; doi:10.1016/S0040-4039(01)83455-9.
  • K.M. Nicholas, R. Pettit: "On the stability of α-(alkynyl)dicobalt hexacarbonyl carbonium ions", in: J. Organomet. Chem., 1972, 44, C21–C24; doi:10.1016/0022-328X(72)80037-8.
  • Blanc, Aurélien; Bochet, Christian G. (2007). "Isotope Effects in Photochemistry: Application to Chromatic Orthogonality" (PDF). Org. Lett. 9 (14): 2649–2651. doi:10.1021/ol070820h. PMID 17555322.
  • Baran, Phil S.; Maimone, Thomas J.; Richter, Jeremy M. (22 March 2007). "Total synthesis of marine natural products without using protecting groups". Nature. 446 (7134): 404–408. Bibcode:2007Natur.446..404B. doi:10.1038/nature05569. PMID 17377577. S2CID 4357378.
  • Synthetic studies of marine alkaloids hapalindoles. Part I Total synthesis of (±)-hapalindoles J and M Tetrahedron, Volume 46, Issue 18, 1990, Pages 6331–6342 Hideaki Muratake and Mitsutaka Natsume doi:10.1016/S0040-4020(01)96005-3
  • Synthetic studies of marine alkaloids hapalindoles. Part 2. Lithium aluminum hydride reduction of the electron-rich carbon-carbon double bond conjugated with the indole nucleus Tetrahedron, Volume 46, Issue 18, 1990, Pages 6343–6350 Hideaki Muratake and Mitsutaka Natsume doi:10.1016/S0040-4020(01)96006-5
  • Synthetic studies of marine alkaloids hapalindoles. Part 3 Total synthesis of (±)-hapalindoles H and U Tetrahedron, Volume 46, Issue 18, 1990, Pages 6351–6360 Hideaki Muratake, Harumi Kumagami and Mitsutaka Natsume doi:10.1016/S0040-4020(01)96007-7
  • T. Reichstein, A. Grüssner: "Eine ergiebige Synthese der L-Ascorbinsäure (C-Vitamin)", in: Helv. Chim. Acta, 1934, 17, pp. 311–328; doi:10.1002/hlca.19340170136.
  • J.M. McClure, Samuel J. Danishefsky: "A novel Heck arylation reaction: rapid access to congeners of FR 900482", in: J. Am. Chem. Soc., 1993, 115, pp. 6094–6100; doi:10.1021/ja00067a026.
  • Merrifield, R. B.; Barany, G.; Cosand, W. L.; Engelhard, M.; Mojsov, S. (1977). "Proceedings of the 5th American Peptide Symposium". Biochemical Education. 7 (4): 93–94. doi:10.1016/0307-4412(79)90078-5.
  • Serge L. Beaucage, Radhakrishman P. Iyer: "Advances in the Synthesis of Oligonucleotides by the Phosphoramidite Approach", in: Tetrahedron, 1992, 48, pp. 2223–2311; doi:10.1016/S0040-4020(01)88752-4.

harvard.edu

ui.adsabs.harvard.edu

nih.gov

pubmed.ncbi.nlm.nih.gov

renyi.hu

  • Gregg B. Fields: Methods for Removing the Fmoc Group. (PDF; 663 kB) In: Michael W. Pennington, Ben M. Dunn (eds.): Peptide Synthesis Protocols volume 35, 1995, ISBN 978-0-89603-273-6, pp. 17–27.

rero.ch

doc.rero.ch

semanticscholar.org

api.semanticscholar.org