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| Methods for the conversion of vinyl sulfides to aldehydes Tetrahedron Letters, Volume 16, Issue 50, 1975, Pages 4437-4440 Albert J. MuraJr., George Majetich, Paul A. Grieco, Theodore Cohen | ||||
| Studies of the stability and reactivity of substituted vinyl titanium triisopropoxides Tetrahedron Letters, Volume 30, Issue 25, 1989, Pages 3271-3274 Robert K. BoeckmanJr., Kenneth J. O'Connor | ||||
−60°C and exhibit excellent chemoselectivity, moderate reactivity, and modest diastereoselectivity.
| Expedient synthesis of α,α-difluorohomopropargylic alcohols from TIPS-difluorobromopropyne via a Zn-mediated propargylation of aldehydes and ketones Tetrahedron Letters, Volume 41, Issue 14, 1 April 2000, Pages 2339-2342 ZhiGang Wang, Gerald B. Hammond | ||||
| Reaction of s-vinyl sulfilimines with carbanions synthesis of β-substituted vinyl sulfides Tetrahedron Letters, Volume 18, Issue 19, 1977, Pages 1659-1660 Tamotsu Yamamoto, Masa-aki Kakimoto, Makoto Okawara | ||||
| Eliminative deoxygenation: A facile synthesis of α-cyano and α-carboalkoxy substituted vinyl sulfides Tetrahedron Letters, Volume 26, Issue 20, 1985, Pages 2395-2398 R. D. Miller, R. Hässig | ||||
| Elongation of carbonyl compounds by utilizing electroreduction as a key step Tetrahedron Letters, Volume 21, Issue 16, 1980, Pages 1545-1548 Tatsuya Shono, Yoshihiro Matsumura, Shigenori Kashimura | ||||
| Unexpected reactivity of oxygenated 2-acyl-1,3-dithianes with electrophiles Tetrahedron Letters, Volume 44, Issue 2, 6 January 2003, Pages 213-216 Michael Smietana, Alain Valleix, Charles Mioskowski | ||||
| Regioselective synthesis of fluoroaldols. Studies toward fluoroepothilones syntheses via antibody catalysis Tetrahedron Letters, Volume 41, Issue 43, 21 October 2000, Pages 8243-8246 Subhash C. Sinha, Shantanu Dutta, Jian Sun | ||||
| Fast and convenient base-mediated synthesis of 3-substituted quinolines Tetrahedron Letters, Volume 50, Issue 2, 14 January 2009, Pages 201-203 Hans Vander Mierde, Pascal Van Der Voort, Francis Verpoort | ||||
| A facile one-pot conversion of non-enolizable aldehydes to diazirines Tetrahedron Letters, Volume 41, Issue 6, 5 February 2000, Pages 795-796 Igor R. Likhotvorik, Eunju Lee Tae, Celine Ventre, Matthew S. Platz | ||||
| Model studies for the synthesis of clavulactone Tetrahedron Letters, Volume 41, Issue 18, 29 April 2000, Pages 3459-3461 Zhihong Zeng, Xingxiang Xu | ||||
| The FeII---FeIV and FeIII---FeV manifolds in an expanded world of Gif chemistry Tetrahedron Letters, Volume 35, Issue 32, 8 August 1994, Pages 5805-5808 Christophe Bardin, Derek H. R. Barton, Bin Hu, Roy Rojas-Wahl, Dennis K. Taylor | ||||
| Total synthesis of 4-F3t-neuroprostane and its 4-epimer Tetrahedron Letters, Volume 50, Issue 13, 1 April 2009, Pages 1498-1500 Anne-Laure Auvinet, Barbara Eignerová, Alexandre Guy, Martin Kotora, Thierry Durand | ||||
| A short synthesis of the bicyclic core of the zaragozic acids Tetrahedron Letters, Volume 39, Issue 43, 22 October 1998, Pages 7853-7856 Pierre Fraisse, Issam Hanna, Jean-Yves Lallemand | ||||
| Synthesis of tetrahydrothiophenes via nucleophilic addition of Harpp's reagent to cyclic carbonates: Application toward the synthesis of breynolide Tetrahedron Letters, Volume 35, Issue 36, 5 September 1994, Pages 6639-6642 Russell J. Linderman, Neil S. Cutshall, Brian T. Becicka | ||||
| Preparation and use of 1-iodoalkyl ylides Tetrahedron Letters, Volume 35, Issue 18, 2 May 1994, Pages 2827-2828 Jie Chen, Tao Wang, Kang Zhao | ||||
| Tellurium tetrachloride as a mild and efficient catalyst for dithioacetalization Tetrahedron Letters, Volume 32, Issue 18, 29 April 1991, Pages 2039-2042 Hiroyuki Tani, Kazunori Masumoto, Tokuo Inamasu, Hitomi Suzuki | ||||
| Two-step solution-phase synthesis of novel quinoxalinones utilizing a UDC (Ugi/de-Boc/cyclize) strategy Tetrahedron Letters, Volume 43, Issue 9, 25 February 2002, Pages 1637-1639 Thomas Nixey, Paul Tempest, Christopher Hulme | ||||
| Two-step solution-phase synthesis of novel benzimidazoles utilizing a UDC (Ugi/de-Boc/cyclize) strategy Tetrahedron Letters, Volume 42, Issue 30, 23 July 2001, Pages 4959-4962 Paul Tempest, Vu Ma, Samuel Thomas, Zheng Hua, Michael G Kelly, Christopher Hulme | ||||
| Efficient synthesis of 3-substituted 2,3-dihydroquinolin-4-ones using a one-pot sequential multi-catalytic process: Pd-catalyzed allylic amination–thiazolium salt-catalyzed Stetter reaction cascade Tetrahedron Letters, Volume 47, Issue 26, 26 June 2006, Pages 4365-4368 Tetsuhiro Nemoto, Tomoaki Fukuda, Yasumasa Hamada | ||||
| Reactivity of transition metal hydrides and thiolates. Reaction of trihydridobis(π-cyclopentadienyl)niobium with dimethyldisulphide and reactions of niobium, molybdenum and tungsten thiolates with alkynes Inorganica Chimica Acta, Volume 43, 1980, Pages 5-10 Jean-L. Le Quere, Francois Y. Petillon, Jacques E. Guerchais, J. Sala-Pala | ||||
| Parallel iterative solution-phase synthesis of 5-amino-1-aryl-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylic acid amide derivatives Tetrahedron Letters, Volume 44, Issue 8, 17 February 2003, Pages 1675-1678 Bernd Brodbeck, Bernd Püllmann, Sébastien Schmitt, Matthias Nettekoven | ||||
| A mild, efficient method for the oxidation of α-diazo-β-hydroxyesters to α-diazo-β-ketoesters Tetrahedron Letters, Volume 49, Issue 19, 5 May 2008, Pages 3162-3164 Puhui Li, Max M. Majireck, Ilia Korboukh, Steven M. Weinreb | ||||
| Enantioselective synthesis of the farnesyltransferase inhibitor, A-345665.0 Tetrahedron Letters, Volume 47, Issue 49, 4 December 2006, Pages 8765-8768 Michael J. Rozema, Michael Fickes, Maureen McLaughlin, Bridget Rohde, Todd McDermott | ||||
| Brønsted- and Lewis acid-catalyzed cyclization giving rise to substituted anthracenes and acridines Tetrahedron Letters, Volume 43, Issue 37, 9 September 2002, Pages 6605-6608 Raf Goossens, Mario Smet, Wim Dehaen | ||||
| Synthesis of side-chain homologated analogs of 1,25-dihydroxycholecalciferol and 1,25-dihydroxyergocalciferol Steroids, Volume 56, Issue 6, June 1991, Pages 311-315 Micha Chodynski, Andrzej Kutner | ||||
| Dialkylzinc additions with a chiral osmaimidazolidine ligand from asymmetric diamination of olefins Tetrahedron Letters, Volume 44, Issue 17, 21 April 2003, Pages 3547-3549 Kilian Muñiz | ||||
| Asymmetric synthesis of (R)- and (S)-2-trifluoromethylepinephrine Tetrahedron Letters, Volume 45, Issue 13, 22 March 2004, Pages 2731-2733 Lun-Cong Dong, Michael Crowe, Jonathan West, Jeffrey R. Ammann | ||||
| Deprotection of thioacetals and 1,3-dithianes with dimethylsulphoxide Tetrahedron Letters, Volume 33, Issue 52, 22 December 1992, Pages 8163-8164 Ch. Srinivasa Rao, M. Chandrasekharam, H. Ila, H. Junjappa | ||||
| Studies in terpenoids—XVII : Synthesis of 7-hydroxycadalenal and some related naturally occurring sesquiterpenoids Tetrahedron, Volume 27, Issue 3, 1971, Pages 645-651 Jose Alexander, G. S. Krishna Rao | ||||
| Measures for Obtaining Inclusive Sets of Area Cladograms under Assumptions Zero, 1, and 2 with Different Methods for Vicariance Biogeography Cladistics, Volume 17, Issue 3, September 2001, Pages 248-259 Marco G. P. van Veller, M. Zandee, D. J. Kornet | ||||
| Ultrasonic relaxation of the conformational equilibria in some substituted vinyl compounds Advances in Molecular Relaxation Processes, Volume 4, Issue 2, October 1972, Pages 193-202 E. Wyn-Jones, K. R. Crook, W. J. Orville-Thomas | ||||
| Solvent free preparation of amidophosphonates from isocyanides Tetrahedron Letters, Volume 47, Issue 23, 5 June 2006, Pages 3945-3947 Laurent El Kaïm, Laurence Grimaud, Simon Hadrot | ||||
| Novel and convenient synthesis of 4(1H)quinolones Tetrahedron Letters, Volume 46, Issue 5, 31 January 2005, Pages 735-737 Jan Tois, Mikko Vahermo, Ari Koskinen | ||||
| A concise enantioselective total synthesis of rhizoxin D Tetrahedron Letters, Volume 43, Issue 3, 14 January 2002, Pages 493-497 Ian S. Mitchell, Gerald Pattenden, Jeffrey P. Stonehouse | ||||
| Efficient syntheses of enantioenriched (R)-pipecolic acid and (R)-proline via electrophilic organocatalytic amination Tetrahedron Letters, Volume 50, Issue 4, 28 January 2009, Pages 492-494 Delphine Kalch, Nicolas De Rycke, Xavier Moreau, Christine Greck | ||||
| Enantiospecific synthesis of (−)-muricatacin from Tetrahedron: Asymmetry, Volume 17, Issue 17, 2 October 2006, Pages 2465-2467 Kavirayani R. Prasad, Pazhamalai Anbarasan | ||||
C31H58O4 [α]D = +2.4 (c 3.4, CHCl3) Source of chirality: Absolute configuration: (4R,5R)
(4S,5S)-4,5-Bis((R)-1-hydroxytridecyl)-2,2-dimethyl-1,3-dioxolane
C31H62O4 [α]D = −2.7 (c 3.6, CHCl3) Source of chirality: Absolute configuration: (4S,5S)
(4S,5S)-4,5-Bis((R)-1-(benzyloxy)tridecyl)-2,2-dimethyl-1,3-dioxolane
C45H74O4 [α]D = −7.9 (c 2.1, CHCl3) Source of chirality: Absolute configuration: (4S,5S)
(R)-5-((R)-1-(Benzyloxy)tridecyl)-dihydrofuran-2(3H)-one
C24H38O3 [α]D = −9.6 (c 3.0, CHCl3) Source of chirality: Absolute configuration: (4R,5R)
(−)-Muricatacin
C17H32O3 [α]D = −23.6 (c 1.1, CHCl3) Source of chirality: Absolute configuration: (4R,5R)
| Design and synthesis of novel pinacolylboronate containing combretastatin ‘antimitotic agent’ analogues Tetrahedron Letters, Volume 50, Issue 25, 24 June 2009, Pages 3031-3034 Bhaskar C. Das, Sakkarapalayam M. Mahalingam, Todd Evans | ||||
| Stereoselective synthesis of iriomoteolide-1a hemiketal core Tetrahedron Letters, Volume 50, Issue 31, 5 August 2009, Pages 4485-4487 Jun Xie, David A. Horne | ||||
| Stereospecific intramolecular formyl transfer via radical cyclization-fragmentation: Preparation of alkyl 2-deoxy-2α-formylglucopyranosides and similar compounds Tetrahedron Letters, Volume 34, Issue 39, 24 September 1993, Pages 6247-6250 Michael E. Jung, S. W. Tina Choe | ||||
| The Vilsmeier reaction on dithioketals: A facile method for the stereoselective synthesis of β-alkylthioethylenic aldehydes Tetrahedron Letters, Volume 35, Issue 16, 18 April 1994, Pages 2585-2586 C. V. Asokan, Annie Mathews | ||||
| Functions Incorporating a Chalcogen and a Silicon, Germanium, Boron, or Metal Comprehensive Organic Functional Group Transformations II, 2005, Chapter 4.08, Pages 357-410 N. G. Bhat | ||||
| Regio- and stereospecific cleavage of α,β-epoxysilanes with lithium phenylsulfide Tetrahedron Letters, Volume 41, Issue 7, 12 February 2000, Pages 1111-1114 Purificación Cuadrado, Ana M. González-Nogal | ||||
| Isolation and characterization of alk-1-enyl alkyl ethers Chemistry and Physics of Lipids, Volume 2, Issue 2, June 1968, Pages 183-195 V. Mahadevan, F. Phillips, C. V. Viswanathan | ||||
| Methods of investigation spectroscopic determination of the composition of bisulphite derivatives of copolymers of acrolein with acrylic acid Polymer Science U.S.S.R., Volume 23, Issue 7, 1981, Pages 1842-1845 M.G. Voronkov, V.Z. Annenkova, N.P. Roman'kova, E.I. Brodskaya, V.M. Annenkova | ||||
| Titanium carbenoid reagents for converting carbonyl groups into alkenes Tetrahedron, Volume 63, Issue 23, 4 June 2007, Pages 4825-4864 Richard C. Hartley, Jianfeng Li, Calver A. Main, Gordon J. McKiernan | ||||
| Recent synthetic developments in a powerful imino Diels–Alder reaction (Povarov reaction): application to the synthesis of N-polyheterocycles and related alkaloids Tetrahedron, Volume 65, Issue 14, 4 April 2009, Pages 2721-2750 Vladimir V. Kouznetsov | ||||
| Organic synthesis with α-chlorosulfides Tetrahedron, Volume 42, Issue 14, 1986, Pages 3731-3752 Brid M. Dilworth, M. Anthony McKervey | ||||
| Stereoselective conversion of lithiated benzylic or allylic 3-methyl-1(Z),3-butadienyl sulfides into cis-disubstituted cyclopropane compounds Tetrahedron Letters, Volume 24, Issue 23, 1983, Pages 2387-2390 Marius Reglier, Sylvestre A. Julia | ||||
| Generation and reaction of an oxiranyl anion derived from α,β-epoxy-γ-butyrolactone Tetrahedron Letters, Volume 40, Issue 41, 8 October 1999, Pages 7367-7370 Kouji Kuramochi, Hideyoshi Itaya, Seigo Nagata, Takao Ken-ichi, Susumu Kobayashi | ||||
| A direct synthesis of 5,6-dihydroindolo[2,1-a]isoquinolines that exhibit immunosuppressive activity Bioorganic & Medicinal Chemistry Letters, In Press, Corrected Proof, Available online 20 August 2009 George A. Kraus, Vinayak Gupta, Marian Kohut, Navrozedeep Singh | ||||
| Graphical abstracts Tetrahedron Letters, Volume 34, Issue 48, 26 November 1993, Pages 7653-7662 | ||||
| Efficient access to chiral trans-2,6-dialkyl-1,2,5,6-tetrahydropyridines via allylation of chiral imines and ring-closing metathesis Tetrahedron Letters, Volume 44, Issue 3, 13 January 2003, Pages 527-530 François-Xavier Felpin, Jacques Lebreton | ||||
| Monomeric ruthenium carbonyls containing 2-substituted pyrazines: From synthesis to catalytic activity in 1-hexene hydroformylation Journal of Molecular Catalysis A: Chemical, Volume 240, Issues 1-2, 3 October 2005, Pages 7-15 M.A. Moreno, M. Haukka, A. Turunen, T.A. Pakkanen | ||||
| Transformation of β-chalcogeno alkenylboranes into tetrasubstituted olefins Tetrahedron, Volume 60, Issue 2, 5 January 2004, Pages 367-381 Julien Gerard, László Hevesi | ||||
| Syntheses of chiral 1,3-disubstituted tetrahydro-β-carbolines via CIAT process: highly stereoselective Pictet–Spengler reaction of Tetrahedron: Asymmetry, Volume 20, Issue 4, 11 March 2009, Pages 430-439 Sen Xiao, Xia Lu, Xiao-Xin Shi, Yu Sun, Li-Li Liang, Xin-Hong Yu, Jing Dong | ||||
C19H26N2O2 Source of chirality: Absolute configuration: (1R,3R) (c 1.6,CHCl3)
(1R,3R)-Methyl 1-(2-methoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C20H20N2O3 Source of chirality: Absolute configuration: (1R,3R) (c 1.5, CHCl3)
(1R,3R)-Methyl 1-(2-ethoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C21H22N2O3 Source of chirality: Absolute configuration: (1R,3R) (c 4.1, CHCl3)
(1R,3R)-Methyl 1-(2-chlorophenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C19H17N2O2Cl Source of chirality: Absolute configuration: (1R,3R) (c 0.9, CHCl3)
(1R,3R)-Methyl 1-methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C14H16N2O2 Source of chirality: Absolute configuration: (1R,3R) (c 2.5, CHCl3)
(1R, 3R)-Methyl 1-ethyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C15H18N2O2 Source of chirality: Absolute configuration: (1R,3R) (c 1.6, CHCl3)
(1S,3R)-Methyl 1-(4-acetoxy-3-methoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C22H22N2O5 Source of chirality: Absolute configuration: (1S,3R) (c 1.2, CHCl3)
(1R,3R)-Methyl 1-(4-benzoyloxy-3-methoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C27H24N2O5 Source of chirality: Absolute configuration: (1R,3R) (c 1.4, CHCl3)
(1R,3R)-Ethyl 1-(3,4,5-trimethoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C23H26N2O5 Source of chirality: Absolute configuration: (1R,3R) (c 0.4, CHCl3)
(1S,3R)-Ethyl 1-(3,4-dimethoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C22H24N2O4 Source of chirality: Absolute configuration: (1S,3R) (c 1.9, CHCl3)
(1S,3R)-Methyl 1-(3,4,5-trimethoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C22H24N2O5 Source of chirality: Absolute configuration: (1S,3R) (c 1.3, CHCl3)
(1S,3R)-Ethyl 1-(4-methoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C21H22N2O3 Source of chirality: Absolute configuration: (1S,3R) (c 0.3, CHCl3)
(1R,3R)-Ethyl 1-(benzo[d][1,3]dioxol-5-yl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C21H20N2O4 Source of chirality: Absolute configuration: (1R,3R) (c 1.0, EtOAc)
C22H22N2O4
(1R,3R)-Propyl 1-(benzo[d][1,3]dioxol-5-yl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate Source of chirality: Absolute configuration: (1R,3R) (c 1.0, EtOAc)
(1R,3R)-Methyl 1-(3,4-dimethoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C21H22N2O4 Source of chirality: Absolute configuration: (1R,3R) (c 1.6, CHCl3)
(1S,3R)-Methyl 1-phenyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C19H18N2O2 Source of chirality: Absolute configuration: (1S,3R) (c 1.0, CHCl3)
(1S,3R)-Methyl 1-deutero-1-(3,4-dimethoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C21H21DN2O4 Source of chirality: Absolute configuration: (1S,3R) (c 1.0, CHCl3)
(R)-Methyl 2-amino-3-(2-(3,4-dimethoxybenzyl)-1H-indol-3-yl)propanoate
C21H24N2O4 Source of chirality: Absolute configuration: (R) (c 1.2, CHCl3)
(1S,3R)-Methyl 1-(3,4-dimethoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C21H22N2O4 Source of chirality: Absolute configuration: (1S,3R) (c 1.7, CHCl3)
(1S,3R)-Methyl 1-(4-methoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C20H20N2O3 Source of chirality: Absolute configuration: (1S,3R) (c 2.0, CHCl3)
(1R,3R)-Methyl 1-phenyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C19H18N2O2 Source of chirality: Absolute configuration: (1R,3R) (c 1.5, CHCl3)
(1R,3R)-Methyl 1-(4-hydroxy-3-methoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C20H20N2O4 Source of chirality: Absolute configuration: (1R,3R) (c 1.1, CHCl3)
(1R,3R)-Methyl 1-(4-hydroxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C19H18N2O3 Source of chirality: Absolute configuration: (1R,3R) (c 1.0, acetone)
(1R,3R)-Methyl 1-(4-nitrophenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C19H17N3O4 Source of chirality: Absolute configuration: (1R,3R) (c 1.0,CHCl3)
(1S,3R)-Methyl 1-isopropyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C16H20N2O2 Source of chirality: Absolute configuration: (1S,3R) (c 1.6, CHCl3)
(1R,3R)-Methyl 1-(2-nitrophenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C19H17N3O4 Source of chirality: Absolute configuration: (1R,3R) (c 6.6,CHCl3)
| Synthesis of fused pyran and arylbis(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)methane in ionic liquid Chinese Chemical Letters, Volume 20, Issue 4, April 2009, Pages 387-390 Xue Sen Fan, Ying Ying Qu, Xin Ying Zhang, Xia Wang, Jian Ji Wang | ||||
| Diastereospecific oxidation of ferrocenyl aminoalcohols: synthesis of new chiral ligands Tetrahedron: Asymmetry, Volume 10, Issue 10, 21 May 1999, Pages 1835-1837 Olivier Delacroix, Sophie Picart-Goetgheluck, Lucien Maciejewski, Jacques Brocard * | ||||
| Optimisation and synthesis of libraries derived from phenolic amino acid scaffolds Tetrahedron Letters, Volume 41, Issue 38, 16 September 2000, Pages 7405-7408 Andrew D. Morley | ||||
| Total synthesis of (±)-luminacin D Tetrahedron, Volume 63, Issue 22, 28 May 2007, Pages 4703-4711 Daniel Oehlrich, Sandrine M.E. Vidot, Mark W. Davies, Guy J. Clarkson, Michael Shipman | ||||
| α-Amido sulfones from natural α-amino acids and their reaction with carbon nucleophiles Tetrahedron, Volume 62, Issue 5, 30 January 2006, Pages 960-967 Marino Petrini, Mirko Seri | ||||
| The kinetics of oxidation of aliphatic aldehydes by chromic acid Tetrahedron Letters, Volume 11, Issue 58, 1970, Pages 5039-5040 Kalyan K. Banerji, C. Goswami | ||||
| Chapter 6 Practical mathematics of multistep reactions Comprehensive Chemical Kinetics, Volume 38, 2001, Pages 119-147 | ||||
| Expeditious synthesis of imidazo[1,2-c]pyrimidines via a [4+1]-cycloaddition Tetrahedron Letters, Volume 48, Issue 12, 19 March 2007, Pages 2213-2216 Michael Umkehrer, Günther Ross, Nadine Jäger, Christoph Burdack, Jürgen Kolb, Hong Hu, Maria Alvim-Gaston, Christopher Hulme | ||||
| Synthesis of oligonucleotide 2′-conjugates via amide bond formation in solution Bioorganic & Medicinal Chemistry Letters, Volume 14, Issue 3, 9 February 2004, Pages 801-804 Anna V. Kachalova, Dmitry A. Stetsenko, Michael J. Gait, Tatiana S. Oretskaya | ||||
| Chapter 6 Practical mathematics of multistep reactions Comprehensive Chemical Kinetics, Volume 40, 2004, Pages 133-161 | ||||
| Organische Synthesen mit Übergangsmetall-Komplexen XLV. 3-Hydroxypyridine, 1H-Pyrrole und 2-Hydroxypyrrol-Derivate aus einem Aminocarben-Chromkomplex und Alkinen Journal of Organometallic Chemistry, Volume 389, Issue 1, 5 June 1990, Pages c1-c6 Rudolf Aumann, Heinrich Heinen | ||||
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