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Schutzgruppe (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Schutzgruppe" in German language version.

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85doi.org
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2,971st place
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  • Dietrich Spitzner, Kai Oesterreich: „Anionically Induced Domino Reactions – Synthesis of a Norpatchoulenol-Type Terpene“, in: European Journal of Organic Chemistry, 2001, 10; S. 1883–1886; doi:10.1002/1099-0690(200105)2001:10<1883::AID-EJOC1883>3.0.CO;2-M.
  • Michael Schelhaas, Herbert Waldmann: „Schutzgruppenstrategien in der organischen Synthese“, in: Angewandte Chemie, 1996, 103, S. 2195–2200; doi:10.1002/ange.19961081805.
  • Naomi Sakai, Yasufumi Ohfune: „Total synthesis of galantin I. Acid-catalyzed cyclization of galantinic acid“, in: J. Am. Chem. Soc., 1992, 114, S. 998–1010; doi:10.1021/ja00029a031.
  • 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, S. 2285–2286; doi:10.1021/jo00405a045.
  • 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, S. 1547–1557; doi:10.1021/ja00213a031.
  • John O. Osby, Michael G. Martin, Bruce Ganem: An Exceptionally Mild Deprotection of Phthalimides, in: Tetrahedron Lett., 1984, 25, S. 2093–2096; doi:10.1016/S0040-4039(01)81169-2.
  • 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, S. 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, S. 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, S. 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, S. 5496–5498; doi:10.1021/jo00019a004.
  • James D. White, Motoji Kawasaki: „Total synthesis of (+)-latrunculin A“, in: J. Am. Chem. Soc., 1990, 112, S. 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, S. 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, S. 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, S. 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, S. 3910–3926; doi:10.1021/ja00036a045.
  • J. F. W. McOmie, D. E. West: 3,3′-Dihyroxybiphenyl In: Organic Syntheses. 49, 1969, S. 50, doi:10.15227/orgsyn.049.0050; Coll. Vol. 5, 1973, S. 412 (PDF).
  • Yuji Oikawa, Tadao Yoshioka, Osamu Yonemitsu: „Specific removal of o-methoxybenzyl protection by DDQ oxidation“, in: Tetrahedron Lett., 1982, 23, S. 885–888; doi:10.1016/S0040-4039(00)86974-9.
  • Rolf Johansson, Bertil Samuelsson: „Regioselective reductive ring-opening of 4-methoxybenzylidene acetals of hexopyranosides. Access to a novel protecting-group strategy. Part 1“, in: J. Chem. Soc., Perkin Trans. 1, 1984, S. 2371–2374; doi:10.1039/P19840002371.
  • Michel Bessodes, Dimitri Komiotis, Kostas Antonakis: „Rapid and selective detritylation of primary alcohols using formic acid“, in: Tetrahedron Lett., 1986, 27, S. 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, S. 10023–10034; doi:10.1016/S0040-4020(01)96051-X.
  • 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, S. 3279–3285; doi:10.1021/ja00297a038.
  • 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, S. 2523–2525; doi:10.1021/ja00242a053.
  • Elias J. Corey, Mark G. Bock: „Protection of primary hydroxyl groups as methylthiomethyl ethers“, in: Tetrahedron Lett., 1975, 16, S. 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, S. 6818–6820; doi:10.1021/ja00388a074.
  • 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, S. 1796–1801; doi:10.1039/P19810001796.
  • 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, S. 7962–7965; doi:10.1021/ja00547a037.
  • W. Clark Still, Dominick Mobilio: „Synthesis of asperdiol“, in: J. Org. Chem., 1983, 48, S. 4785–4786; doi:10.1021/jo00172a070.
  • Masahiro Hirama, Mitsuko Uei: „A chiral total synthesis of compactin“, in: J. Am. Chem. Soc., 1982, 104, S. 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, S. 625–627; doi:10.1021/ja00341a055.
  • Robert C. Gadwood, Renee M. Lett, Jane E. Wissinger: „Total synthesis of (±)-poitediol and (±)4-epipoitediol“, in: J. Am. Chem. Soc., 1984, 106, S. 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, S. 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, S. 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, S. 3671–3672; doi:10.1021/jo00193a051.
  • 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, S. 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, S. 1942–1943; doi:10.1021/ja00474a058.
  • Christopher R. Schmid, Jerry D. Bryant: D-(R)-Glycerinaldehyde Acetonide In: Organic Syntheses. 72, 1995, S. 6, doi:10.15227/orgsyn.072.0006; Coll. Vol. 9, 1998, S. 450 (PDF).
  • 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, S. 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, S. 4274–4282 doi:10.1021/jo00253a020.
  • T. Tsunoda, M. Suzuki, R. Noyori: „A facile procedure for acetalization under aprotic conditions“, in: Tetrahedron Lett., 1980, 21, S. 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, S. 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, S. 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, S. 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, S. 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, S. 3850–3866; doi:10.1021/ja00010a030.
  • Satomi Niwayama: „Highly Efficient Selective Monohydrolysis of Symmetric Diesters“, in: J. Org. Chem., 2000, 65, S. 5834–5836; doi:10.1021/jo0001986.
  • Robert V. Stevens, Albert W. M. Lee: „Stereochemistry of the Robinson-Schoepf reaction. A stereospecific total synthesis of the ladybug defense alkaloids precoccinelline and coccinelline“, in: J. Am. Chem. Soc., 1979, 101, S. 7032–7035; doi:10.1021/ja00517a042.
  • J. Wrobel, K. Takahashi, V. Honkan, G. Lannoye, J. M. Cook, Steven H. Bertz: „α-Lithio ketones. 1. Stereocontrolled synthesis of (±)-modhephene via the Weiss reaction“, in: J. Org. Chem., 1983, 48, S. 139–141; doi:10.1021/jo00149a034.
  • Dennis D. Keith, John A. Tortora, Roxana Yang: „Synthesis of L-2-amino-4-methoxy-trans-but-3-enoic acid“, in: J. Org. Chem., 1978, 43, S. 3711–3713; doi:10.1021/jo00413a016.
  • 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, S. 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, S. 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, S. 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, S. 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, S. 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, S. 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, S. 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, S. 3573–3576; doi:10.1016/S0040-4039(00)88171-X.
  • Elias J. Corey, Plato A. Magriotis: „Total synthesis and absolute configuration of 7,20-diisocyanoadociane“, in: J. Am. Chem. Soc., 1987, 109, S. 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, S. 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, S. 3051–3054; doi:10.1016/S0040-4039(01)94936-6.
  • 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, S. 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, S. 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, S. 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, S. 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, S. 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, S. 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, S. 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, S. 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, S. 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, S. 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, S. 4133–4170; doi:10.1016/S0040-4020(02)00315-0.
  • Kenneth M. Nicholas, R. Pettit: „An alkyne protection group“, in: Tetrahedron Lett., 1971, 37, S. 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, S. 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.
  • T. Reichstein, A. Grüssner: „Eine ergiebige Synthese der L-Ascorbinsäure (C-Vitamin)“, in: Helv. Chim. Acta, 1934, 17, S. 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, S. 6094–6100; doi:10.1021/ja00067a026.
  • Serge L. Beaucage, Radhakrishman P. Iyer: „Advances in the Synthesis of Oligonucleotides by the Phosphoramidite Approach“, in: Tetrahedron, 1992, 48, S. 2223–2311; doi:10.1016/S0040-4020(01)88752-4.
  • Michael Schelhaas, Herbert Waldmann: „Schutzgruppenstrategien in der organischen Synthese“, in: Angewandte Chemie, 1996, 103, S. 2194; doi:10.1002/ange.19961081805.
  • Marco Eissen, Radoslaw Mazur, Heinz-Georg Quebbemann und Karl-Heinz Pennemann: „Atom Economy and Yield of Synthesis Sequences“, in: Helv. Chim. Acta, 2004, 87, S. 524–535; doi:10.1002/hlca.200490050.
  • Marco Eissen, Jürgen O. Metzger: „Environmental Performance Metrics for Daily Use in Synthetic Chemistry“, in: Chemistry – A European Journal, 2002, 8, S. 3580–3585; doi:10.1002/chin.200247273.
  • Marco Eissen, Jürgen O. Metzger, Eberhard Schmidt, Uwe Schneidewind: 10 Jahre nach „Rio“ – Konzepte zum Beitrag der Chemie zu einer nachhaltigen Entwicklung, in: Angewandte Chemie, 2002, 114, S. 402–425; doi:10.1002/1521-3757(20020201)114:3<402::AID-ANGE402>3.0.CO;2-D.
  • Hideaki Muratake, Harumi Kumagami, Mitsutaka Natsume: Synthetic studies of marine alkaloids hapalindoles. Part 3 Total synthesis of (±)-hapalindoles H and U, in: Tetrahedron, 1990, 46, S. 6351–6360; doi:10.1016/S0040-4020(01)96007-7.
  • Hideaki Muratake, Mitsutaka Natsume: Synthetic studies of marine alkaloids hapalindoles. Part I Total synthesis of (±)-hapalindoles J and M, in: Tetrahedron, 1990, 46, S. 6331–6342; doi:10.1016/S0040-4020(01)96005-3.
  • Hideaki Muratake, Mitsutaka Natsume: 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, in: Tetrahedron, 1990, 46, S. 6343–6350; doi:10.1016/S0040-4020(01)96006-5.
  • Phil S. Baran, Thomas J. Maimone, Jeremy M. Richter: Total synthesis of marine natural products without using protecting groups, in: Nature, 446, S. 404–408; doi:10.1038/nature05569.

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