Recent Advancements in Stereoselective Olefin Metathesis Using Ruthenium Catalysts
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[1] J. Sanders,et al. The Future of Ethenolysis in Biobased Chemistry. , 2017, ChemSusChem.
[2] R. Grubbs,et al. Z-Selective Cross-Metathesis and Homodimerization of 3E-1,3-Dienes: Reaction Optimization, Computational Analysis, and Synthetic Applications. , 2016, Journal of the American Chemical Society.
[3] C. Bruneau,et al. Ethenolysis: A Green Catalytic Tool to Cleave Carbon-Carbon Double Bonds. , 2016, Chemistry.
[4] Mylène de Léséleuc,et al. Catalytic Macrocyclization Strategies Using Continuous Flow: Formal Total Synthesis of Ivorenolide A. , 2016, The Journal of organic chemistry.
[5] Vidar R. Jensen,et al. Phosphine-Based Z-Selective Ruthenium Olefin Metathesis Catalysts , 2016 .
[6] R. Grubbs,et al. Tandem Olefin Metathesis/Oxidative Cyclization: Synthesis of Tetrahydrofuran Diols from Simple Olefins. , 2016, Journal of the American Chemical Society.
[7] R. Schrock,et al. Kinetically controlled E-selective catalytic olefin metathesis , 2016, Science.
[8] Richard L. Pederson,et al. High Trans Kinetic Selectivity in Ruthenium-Based Olefin Cross-Metathesis through Stereoretention. , 2016, Organic letters.
[9] C. Costabile,et al. Ruthenium olefin metathesis catalysts featuring unsymmetrical N-heterocyclic carbenes. , 2016, Dalton transactions.
[10] T. Donohoe,et al. Application of catalytic Z-selective olefin metathesis in natural product synthesis , 2015 .
[11] M. Buchmeiser,et al. Molybdenum Imido Alkylidene and Tungsten Oxo Alkylidene N‐Heterocyclic Carbene Complexes for Olefin Metathesis , 2015 .
[12] G. Clarkson,et al. Ring closing metathesis reactions of α-methylene-β-lactams: application to the synthesis of a simplified phyllostictine analogue with herbicidal activity. , 2015, Organic & biomolecular chemistry.
[13] R. Grubbs,et al. Tandem Z-Selective Cross-Metathesis/Dihydroxylation: Synthesis of anti-1,2-Diols. , 2015, Angewandte Chemie.
[14] R. Grubbs,et al. Cyclometalated Z-Selective Ruthenium Metathesis Catalysts with Modified N-Chelating Groups , 2015 .
[15] Shane L. Mangold,et al. Stereoselective synthesis of macrocyclic peptides via a dual olefin metathesis and ethenolysis approach , 2015, Chemical science.
[16] R. Grubbs,et al. Z-selective cross metathesis with ruthenium catalysts: synthetic applications and mechanistic implications. , 2015, Angewandte Chemie.
[17] Malte S. Mikus,et al. High-value alcohols and higher-oxidation-state compounds by catalytic Z-selective cross-metathesis , 2015, Nature.
[18] R. Grubbs,et al. Z-Selective Ruthenium Metathesis Catalysts: Comparison of Nitrate and Nitrite X-type Ligands. , 2014, Polyhedron.
[19] R. Schrock,et al. Catalyst-controlled stereoselective olefin metathesis as a principal strategy in multistep synthesis design: a concise route to (+)-neopeltolide. , 2014, Angewandte Chemie.
[20] V. Bertolasi,et al. Novel Olefin Metathesis Ruthenium Catalysts Bearing Backbone-Substituted Unsymmetrical NHC Ligands , 2014 .
[21] A. Hoveyda,et al. Reactivity and selectivity differences between catecholate and catechothiolate Ru complexes. Implications regarding design of stereoselective olefin metathesis catalysts. , 2014, Journal of the American Chemical Society.
[22] R. Grubbs,et al. Ru-Based Z-Selective Metathesis Catalysts with Modified Cyclometalated Carbene Ligands. , 2014, Chemical science.
[23] R. Grubbs,et al. Enantioselective Olefin Metathesis with Cyclometalated Ruthenium Complexes , 2014, Journal of the American Chemical Society.
[24] Shane L. Mangold,et al. Z-Selective Olefin Metathesis on Peptides: Investigation of Side-Chain Influence, Preorganization, and Guidelines in Substrate Selection , 2014, Journal of the American Chemical Society.
[25] Vidar R. Jensen,et al. Theory-assisted development of a robust and Z-selective olefin metathesis catalyst. , 2014, Dalton transactions.
[26] A. Hoveyda. Evolution of Catalytic Stereoselective Olefin Metathesis: From Ancillary Transformation to Purveyor of Stereochemical Identity , 2014, The Journal of organic chemistry.
[27] R. Grubbs,et al. Cyclometalated Ruthenium Alkylidene Complexes: A Powerful Family of Z -Selective Olefin Metathesis Catalysts , 2014 .
[28] R. Grubbs,et al. Catalytic, enantioselective synthesis of 1,2-anti-diols by asymmetric ring-opening/cross-metathesis. , 2014, Angewandte Chemie.
[29] A. Hoveyda,et al. Broadly applicable Z- and diastereoselective ring-opening/cross-metathesis catalyzed by a dithiolate ru complex. , 2014, Angewandte Chemie.
[30] C. Bruneau,et al. Z Selectivity: Recent Advances in one of the Current Major Challenges of Olefin Metathesis , 2013 .
[31] R. Grubbs,et al. Ruthenium-catalysed Z-selective cross metathesis of allylic-substituted olefins , 2013, Chemical science.
[32] B. Schmidt,et al. Assisted Tandem Catalytic Cross Metathesis—Oxidation: In One Flask from Styrenes to 1,2‐Diketones and Further to Quinoxalines. , 2013 .
[33] R. Grubbs,et al. Investigations into Ruthenium Metathesis Catalysts with Six-Membered Chelating NHC Ligands: Relationship between Catalyst Structure and Stereoselectivity. , 2013, Organometallics.
[34] Joseph S. Carlson,et al. A synthesis of the chlorosulfolipid mytilipin A via a longest linear sequence of seven steps. , 2013, Angewandte Chemie.
[35] R. Grubbs,et al. Alkene chemoselectivity in ruthenium-catalyzed Z-selective olefin metathesis. , 2013, Angewandte Chemie.
[36] B. G. Davis,et al. Rapid Cross-Metathesis for Reversible Protein Modifications via Chemical Access to Se-Allyl-selenocysteine in Proteins , 2013, Journal of the American Chemical Society.
[37] R. Grubbs,et al. Highly Z-selective and enantioselective ring-opening/cross-metathesis catalyzed by a resolved stereogenic-at-Ru complex. , 2013, Journal of the American Chemical Society.
[38] A. Hoveyda,et al. Readily accessible and easily modifiable Ru-based catalysts for efficient and Z-selective ring-opening metathesis polymerization and ring-opening/cross-metathesis. , 2013, Journal of the American Chemical Society.
[39] K. Woźniak,et al. Testing New Ruthenium Complexes bearing Chiral 1,2,4-Triazol-5-ylidene Ligands as Catalysts for Asymmetric Olefin Metathesis , 2013, Synlett.
[40] Yao-Wei Zhang,et al. Stereoselective synthesis of Z-alkenes. , 2013, Topics in current chemistry.
[41] R. Grubbs,et al. Z-Selective ethenolysis with a ruthenium metathesis catalyst: experiment and theory. , 2013, Journal of the American Chemical Society.
[42] V. R. Jensen,et al. Simple and highly Z-selective ruthenium-based olefin metathesis catalyst. , 2013, Journal of the American Chemical Society.
[43] R. Grubbs,et al. Highly active ruthenium metathesis catalysts exhibiting unprecedented activity and Z-selectivity. , 2013, Journal of the American Chemical Society.
[44] R. Grubbs,et al. Stereoselective access to Z and E macrocycles by ruthenium-catalyzed Z-selective ring-closing metathesis and ethenolysis. , 2013, Journal of the American Chemical Society.
[45] Richard L. Pederson,et al. Concise syntheses of insect pheromones using Z-selective cross metathesis. , 2013, Angewandte Chemie.
[46] Jian-Ping Zuo,et al. Ivorenolide A, an unprecedented immunosuppressive macrolide from Khaya ivorensis: structural elucidation and bioinspired total synthesis. , 2012, Journal of the American Chemical Society.
[47] Xiaotai Wang,et al. A Thorough DFT Study of the Mechanism of Homodimerization of Terminal Olefins through Metathesis with a Chelated Ruthenium Catalyst: From Initiation to Z Selectivity to Regeneration , 2012 .
[48] A. Hoveyda,et al. Z- and enantioselective ring-opening/cross-metathesis with enol ethers catalyzed by stereogenic-at-Ru carbenes: reactivity, selectivity, and Curtin-Hammett kinetics. , 2012, Journal of the American Chemical Society.
[49] A. Hoveyda,et al. Synthesis, isolation, characterization, and reactivity of high-energy stereogenic-at-Ru carbenes: stereochemical inversion through olefin metathesis and other pathways. , 2012, Journal of the American Chemical Society.
[50] S. Blechert,et al. Asymmetric catalysts for stereocontrolled olefin metathesis reactions. , 2012, Chemical Society reviews.
[51] A. Minnaard,et al. Z‐Selectivity: A Novel Facet of Metathesis , 2012 .
[52] R. Grubbs,et al. Z-Selectivity in olefin metathesis with chelated Ru catalysts: computational studies of mechanism and selectivity. , 2012, Journal of the American Chemical Society.
[53] R. Grubbs,et al. Improved ruthenium catalysts for Z-selective olefin metathesis. , 2012, Journal of the American Chemical Society.
[54] R. Schrock,et al. Z-Selective olefin metathesis reactions promoted by tungsten oxo alkylidene complexes. , 2011, Journal of the American Chemical Society.
[55] S. Schreiber,et al. Control of Olefin Geometry in Macrocyclic Ring‐Closing Metathesis Using a Removable Silyl Group. , 2011 .
[56] S. Shuto,et al. One‐Pot Ring‐Closing Metathesis (RCM)/Oxidation by an Assisted Tandem Ruthenium Catalysis for the Synthesis of 2‐Quinolones , 2011 .
[57] R. Schrock. Synthesis of stereoregular ROMP polymers using molybdenum and tungsten imido alkylidene initiators. , 2011, Dalton transactions.
[58] R. Grubbs,et al. Z-selective homodimerization of terminal olefins with a ruthenium metathesis catalyst. , 2011, Journal of the American Chemical Society.
[59] R. Grubbs,et al. Chelated ruthenium catalysts for Z-selective olefin metathesis. , 2011, Journal of the American Chemical Society.
[60] A. Fürstner,et al. Stereoselective synthesis of E,Z-configured 1,3-dienes by ring-closing metathesis. Application to the total synthesis of lactimidomycin. , 2011, Journal of the American Chemical Society.
[61] B. Schmidt,et al. A single precatalyst tandem RCM-allylic oxidation sequence. , 2011, Chemical communications.
[62] S. Blechert,et al. A novel ligand for the enantioselective ruthenium-catalyzed olefin metathesis. , 2011, Angewandte Chemie.
[63] F. Matsuda,et al. Asymmetric total synthesis of danicalipin A and evaluation of biological activity. , 2011, Organic letters.
[64] F. Verpoort,et al. Ruthenium‐Based Olefin Metathesis Catalysts Derived from Alkynes , 2010 .
[65] R. Grubbs,et al. Facile Synthesis of Effcient and Selective Ruthenium Olefin Metathesis Catalysts with Sulfonate and Phosphate Ligands , 2010 .
[66] J. Kim,et al. Lipase-Catalyzed Transesterification as a Practical Route to Homochiral Acyclic anti-1,2-Diols. A New Synthesis of (+)- and (-)- endo-Brevicomin. , 2010 .
[67] S. Blechert,et al. Highly active chiral ruthenium-based metathesis catalysts through a monosubstitution in the N-heterocyclic carbene. , 2010, Angewandte Chemie.
[68] C. Meyer,et al. Metathesis in Natural Product Synthesis: Strategies, Substrates and Catalysts , 2010 .
[69] Tetsuaki Tanaka,et al. Asymmetric total synthesis of (+)-hexachlorosulfolipid, a cytotoxin isolated from Adriatic mussels. , 2010, The Journal of organic chemistry.
[70] Asami Saito,et al. A concise total synthesis of (+)-neopeltolide. , 2010, Angewandte Chemie.
[71] Brice Stenne,et al. Desymmetrizations forming tetrasubstituted olefins using enantioselective olefin metathesis. , 2010, Organic letters.
[72] R. Grubbs,et al. Ruthenium-based heterocyclic carbene-coordinated olefin metathesis catalysts. , 2010, Chemical reviews.
[73] W. Gerwick,et al. A concise enantioselective synthesis of the chlorosulfolipid malhamensilipin A. , 2010, Journal of the American Chemical Society.
[74] K. Grela,et al. Ruthenium-Based Olefin Metathesis Catalysts Bearing N-Heterocyclic Carbene Ligands , 2009 .
[75] R. Schrock,et al. Highly Z-selective metathesis homocoupling of terminal olefins. , 2009, Journal of the American Chemical Society.
[76] Xavier Guinchard,et al. Total synthesis of the antiproliferative macrolide (+)-neopeltolide. , 2009, Organic letters.
[77] Hee‐Yoon Lee,et al. A Facile Total Synthesis of (‐)‐Frontalin, (‐)‐endo‐Brevicomin and (‐)‐exo‐Brevicomin Through PtCl4 Catalyzed Hydroalkoxylation Reaction. , 2009 .
[78] G. Langley,et al. Total synthesis and stereochemical assignment of cis-uvariamicin I and cis-reticulatacin. , 2009, The Journal of organic chemistry.
[79] P. Guiry,et al. Microwave-assisted synthesis of substituted tetrahydropyrans catalyzed by ZrCl4 and its application in the asymmetric synthesis of exo- and endo-brevicomin. , 2009, The Journal of organic chemistry.
[80] W. Gerwick,et al. Relative stereochemistry determination and synthesis of the major chlorosulfolipid from Ochromonas danica. , 2009, Journal of the American Chemical Society.
[81] R. Schrock,et al. Z-selective olefin metathesis processes catalyzed by a molybdenum hexaisopropylterphenoxide monopyrrolide complex. , 2009, Journal of the American Chemical Society.
[82] R. Schrock,et al. Highly Z- and enantioselective ring-opening/cross-metathesis reactions catalyzed by stereogenic-at-Mo adamantylimido complexes. , 2009, Journal of the American Chemical Society.
[83] E. Carreira,et al. Total synthesis of a chlorosulpholipid cytotoxin associated with seafood poisoning , 2009, Nature.
[84] Tetsuaki Tanaka,et al. Enantiocontrolled synthesis of polychlorinated hydrocarbon motifs: a nucleophilic multiple chlorination process revisited. , 2009, The Journal of organic chemistry.
[85] Stuart R. Dubberley,et al. Thermal decomposition modes for four-coordinate ruthenium phosphonium alkylidene olefin metathesis catalysts. , 2008, Chemistry.
[86] I. Paterson,et al. Total synthesis of the marine macrolide (+)-neopeltolide. , 2008, Chemical communications.
[87] H. Fuwa,et al. Total Synthesis of (+)‐Neopeltolide. , 2008 .
[88] C. Vanderwal,et al. Stereoselective dichlorination of allylic alcohol derivatives to access key stereochemical arrays of the chlorosulfolipids. , 2008, Journal of the American Chemical Society.
[89] E. Gallo,et al. Ruthenium-Based Complexes Bearing Saturated Chiral N-Heterocyclic Carbene Ligands: Dynamic Behavior and Catalysis , 2008 .
[90] Min Sang Kwon,et al. Total Synthesis of (+)‐Neopeltolide by a Prins Macrocyclization. , 2008 .
[91] B. Plietker,et al. Diastereoselective Ru‐Catalyzed Cross‐Metathesis—Dihydroxylation Sequence. An Efficient Approach Toward Enantiomerically Enriched syn‐Diols. , 2008 .
[92] Wenjiao Song,et al. Selective functionalization of a genetically encoded alkene-containing protein via "photoclick chemistry" in bacterial cells. , 2008, Journal of the American Chemical Society.
[93] J. Errey,et al. Facile conversion of cysteine and alkyl cysteines to dehydroalanine on protein surfaces: versatile and switchable access to functionalized proteins. , 2008, Journal of the American Chemical Society.
[94] F. Diederich,et al. Modern Supramolecular Chemistry: Strategies for Macrocycle Synthesis , 2008 .
[95] K. Scheidt,et al. Total synthesis and structural revision of the marine macrolide neopeltolide. , 2008, Journal of the American Chemical Society.
[96] Paul S. Ralifo,et al. Total synthesis and stereochemical reassignment of (+)-neopeltolide. , 2007, Angewandte Chemie.
[97] S. Collins,et al. A Highly Active Chiral Ruthenium-Based Catalyst for Enantioselective Olefin Metathesis. , 2007 .
[98] Vincenzo Piccialli,et al. Oxidative cyclization of dienes and polyenes mediated by transition-metal-oxo species , 2007 .
[99] S. Collins,et al. A Highly Active Chiral Ruthenium-Based Catalyst for Enantioselective Olefin Metathesis , 2007 .
[100] J. L. Snelgrove,et al. Tandem ROMP-hydrogenation with a third-generation Grubbs catalyst. , 2007, Journal of the American Chemical Society.
[101] Peter J McCarthy,et al. Neopeltolide, a macrolide from a lithistid sponge of the family Neopeltidae. , 2007, Journal of natural products.
[102] Jeffrey S. Moore,et al. Alkyne Metathesis: Catalysts and Synthetic Applications , 2007 .
[103] R. Grubbs,et al. Highly active chiral ruthenium catalysts for asymmetric cross- and ring-opening cross-metathesis. , 2006, Angewandte Chemie.
[104] M. Snapper,et al. Ruthenium-catalyzed tandem olefin metathesis-oxidations. , 2006, Organic letters.
[105] Sung‐Gon Kim,et al. Efficient total synthesis of (+)-exo-, (−)-endo-brevicomin and their derivatives via asymmetric organocatalysis and olefin cross-metathesis , 2006 .
[106] M. Snapper,et al. Tandem Catalysis: Generating Multiple Contiguous Carbon—Carbon Bonds Through a Ruthenium-Catalyzed Ring-Closing Metathesis/Kharasch Addition. , 2006 .
[107] S. Blechert,et al. Sequential catalysis: a metathesis/dihydroxylation sequence. , 2006, Angewandte Chemie.
[108] R. Grubbs,et al. Highly active chiral ruthenium catalysts for asymmetric ring-closing olefin metathesis. , 2006, Journal of the American Chemical Society.
[109] M. Snapper,et al. Preparation of alkenyl cyclopropanes through a ruthenium-catalyzed tandem enyne metathesis-cyclopropanation sequence. , 2006, Journal of the American Chemical Society.
[110] A. Hoveyda,et al. A readily available chiral Ag-based N-heterocyclic carbene complex for use in efficient and highly enantioselective Ru-catalyzed olefin metathesis and Cu-catalyzed allylic alkylation reactions. , 2005, Journal of the American Chemical Society.
[111] Dennis G. Gillingham,et al. Efficient enantioselective synthesis of functionalized tetrahydropyrans by Ru-catalyzed asymmetric ring-opening metathesis/cross-metathesis (AROM/CM). , 2004, Journal of the American Chemical Society.
[112] C. Dell’Aversano,et al. A new cytotoxic polychlorinated sulfolipid from contaminated Adriatic mussels , 2004 .
[113] A. Quesada,et al. Potential for Use of Synthetic Sex Pheromone for Mating Disruption of the Olive Pyralid Moth, Euzophera pinguis , 2004, Journal of Chemical Ecology.
[114] K. Burdett,et al. Renewable monomer feedstocks via olefin metathesis: Fundamental mechanistic studies of methyl oleate ethenolysis with the first-generation grubbs catalyst , 2004 .
[115] Dennis G. Gillingham,et al. Chiral Ru‐Based Complexes for Asymmetric Olefin Metathesis: Enhancement of Catalyst Activity Through Steric and Electronic Modifications. , 2004 .
[116] R. Schrock,et al. Molybdenum and tungsten imido alkylidene complexes as efficient olefin-metathesis catalysts. , 2003, Angewandte Chemie.
[117] T. Řezanka,et al. Chagosensine, a new chlorinated macrolide from the Red Sea sponge Leucetta chagosensis , 2003 .
[118] R. Grubbs,et al. A general model for selectivity in olefin cross metathesis. , 2003, Journal of the American Chemical Society.
[119] R. Grubbs,et al. Synthesis and activity of ruthenium alkylidene complexes coordinated with phosphine and N-heterocyclic carbene ligands. , 2003, Journal of the American Chemical Society.
[120] M. Snapper,et al. New tandem catalysis: preparation of cyclic enol ethers through a ruthenium-catalyzed ring-closing metathesis-olefin isomerization sequence. , 2002, Journal of the American Chemical Society.
[121] C. Dell’Aversano,et al. Structure and stereochemistry of a new cytotoxic polychlorinated sulfolipid from Adriatic shellfish. , 2002, Journal of the American Chemical Society.
[122] Richard L. Pederson,et al. Applications of Olefin Cross Metathesis to Commercial Products , 2002 .
[123] A. Hoveyda,et al. A recyclable chiral Ru catalyst for enantioselective olefin metathesis. Efficient catalytic asymmetric ring-opening/cross metathesis in air. , 2002, Journal of the American Chemical Society.
[124] R. Schrock. High Oxidation State Multiple Metal—Carbon Bonds , 2002 .
[125] R. Grubbs,et al. Tandem catalysis: the sequential mediation of olefin metathesis, hydrogenation, and hydrogen transfer with single-component Ru complexes. , 2001, Journal of the American Chemical Society.
[126] Tamar Frankel. [The theory and the practice...]. , 2001, Tijdschrift voor diergeneeskunde.
[127] R. Grubbs,et al. Enantioselective ruthenium-catalyzed ring-closing metathesis. , 2001, Organic letters.
[128] R. Grubbs,et al. The Development of L2X2R=CHR Olefin Metathesis Catalysts: An Organometallic Success Story , 2001 .
[129] Theocharis V. Koftis,et al. A Concise Synthesis of (-)-endo-Brevicomin , 2001 .
[130] W. Donk,et al. Convergent synthesis of peptide conjugates using dehydroalanines for chemoselective ligations. , 2001, Organic letters.
[131] R. Schrock,et al. Catalytic asymmetric olefin metathesis. , 2001, Chemistry.
[132] P. Ciminiello,et al. Structural elucidation of a new cytotoxin isolated from mussels of the Adriatic sea. , 2001, The Journal of organic chemistry.
[133] A. Fürstner. Olefin Metathesis and Beyond , 2000 .
[134] J. V. Hest,et al. Efficient incorporation of unsaturated methionine analogues into proteins in vivo , 2000 .
[135] W. Goldring,et al. Cytotoxic Alkaloids Motuporamines A—C: Synthesis and Structural Verification. , 2000 .
[136] C. M. Beaudry,et al. Desymmetrization by ring-closing metathesis leading to 6,8-dioxabicyclo[3.2.1]octanes: a new route for the synthesis of (+)-exo- and endo-brevicomin. , 1999, Organic letters.
[137] V. Odinokov,et al. Insect pheromones and their analogs LIX. A new method for the synthesis of components of the sex pheromones of insects of the genusMalacosoma , 1999, Chemistry of Natural Compounds.
[138] David E. Williams,et al. Motuporamines A—C, Cytotoxic Alkaloids Isolated from the Marine Sponge Xestospongia exigua (Kirkpatrick). , 1998 .
[139] Vincenzo Piccialli,et al. OsO4-Catalyzed oxidative cyclization of geranyl and neryl acetate to cis-2,5-bis(hydroxymethyl)tetrahydrofurans , 1998 .
[140] P. Howse,et al. Insect Pheromones and their Use in Pest Management , 1997, Springer Netherlands.
[141] P. Knochel,et al. Enantioselective Synthesis of Protected α‐Hydroxy Aldehydes and Related 1,2‐Amino Alcohols. Applications to the Synthesis of (‐)‐exo‐ and (‐)‐endo‐Brevicomin. , 1996 .
[142] H. Scharf,et al. D-Erythronolactone and 2,3-O-Isopropylidene-L-erythrose as C4 Building Units: An Efficient Synthesis of Both Enantiomers of endo-Brevicomin and Its 7-Vinyl Analogues. , 1995 .
[143] H. Scharf,et al. D‐Erythronolactone and 2,3‐O‐Isopropylidene‐L‐erythrose as C4 Building Units: An Efficient Synthesis of both Enantiomers of endo‐Brevicomin and its 7‐Vinyl Analogues , 1994 .
[144] J. Soderquist,et al. (+)-Exo-brevicomin via an organometallic boulevard , 1993 .
[145] C. Paolucci,et al. Dihyro- and tetrahydrofuran building blocks from 1,4:3,6-dianhydromannitol. 1. Synthesis of (1S,5R,7R)-endo-(-)- and (1S,5R,7S)-(-)-exo-brevicomin and (R)-(+)-dodecanolide , 1993 .
[146] M. Leconte,et al. A Cyclometalated Aryloxy(chloro)neopentylidenetungsten Complex: A Highly Active and Stereoselective Catalyst for the Metathesis of cis‐ and trans‐2‐Pentene, Norbornene, 1‐Methyl‐norbornene, and Ethyl Oleate , 1992 .
[147] Y. Noda,et al. A short synthesis of (+)-endo-brevicomin. , 1989 .
[148] C. R. Unelius,et al. A Stereospecific Synthesis of All Four Isomers of 9,11-Tetradecadienyl Acetate Using a General Method Applicable to 1,3-Dienes. , 1987 .
[149] B. Johnston,et al. Synthesis of the enantiomers of endo-brevicomin , 1987 .
[150] J. Mulzer,et al. Enantio- and Diastereocontrolled Synthesis of Chiral 1,2-Diol Derivatives from (R)-2,3-Di-O-isopropylideneglyceraldehyde: endo- and exo-Brevicomin. , 1986 .
[151] A. Yusufoglu,et al. Enantioselective synthesis and absolute configuration of both enantiomers of endo-brevicomin , 1986 .
[152] V. Martín,et al. A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compounds , 1981 .
[153] J. Basset,et al. Metathese des olefines avec les precurseurs zerovalents du tungstene (W(CO)5L, L = CO, PPh3, P(OPh)3, P(n-C4H9)3) associes a C2H5AlCl2 et O2. Une etude infrarouge , 1977 .
[154] Par Jean‐Louis Hérisson,et al. Catalyse de transformation des oléfines par les complexes du tungstène. II. Télomérisation des oléfines cycliques en présence d'oléfines acycliques , 1971 .
[155] L. E. Browne,et al. Brevicomin: Principal Sex Attractant in the Frass of the Female Western Pine Beetle , 1968, Science.
[156] H. Brown,et al. Hydroboration. XVIII. The Reaction of Diisopinocampheylborane with Representative cis-Acyclic, Cyclic, and Bicyclic Olefins. A Convenient Systhesis of Optically Active Alcohols and Olefins of High Optical Purity and Established Configuration , 1964 .
[157] A. S. Hay. Oxidative Coupling of Acetylenes. II1 , 1962 .
[158] I. Robinson,et al. Polynorbornene by Coördination Polymerization1 , 1960 .
[159] J. Schreiber. Scent And Chemistry The Molecular World Of Odors , 2016 .
[160] R. Schrock. Metathesis by Molybdenum and Tungsten Catalysts. , 2015, Chimia (Basel).
[161] P. Davies,et al. Alkyne metathesis. , 2005, Chemical communications.
[162] T. Ando,et al. Lepidopteran sex pheromones. , 2004, Topics in current chemistry.
[163] T. Szymańska-Buzar,et al. Ring opening metathesis polymerisation and related chemistry : state of the art and visions for the new century , 2002 .
[164] R. Grubbs,et al. The development of L2X2Ru=CHR olefin metathesis catalysts: an organometallic success story. , 2001, Accounts of chemical research.
[165] Z. Gu,et al. ABSOLUTE STEREOCHEMISTRIES OF SYLVATICIN AND 12, 15-CIS- SYLVATICIN, BIOACTIVE C-20, 23-CIS NON-ADJACENT BIS-TETRAHYDROFURAN ANNONACEOUS ACETOGENINS, FROM ROLLINIA MUCOSA , 1995 .
[166] S. Servi,et al. Hydrolytic and reductive action of fermenting yeast on a keto acetate: synthesis of (+)-endo-brevicomin , 1991 .
[167] Kazutsugu Matsumoto,et al. Synthesis of (+)-endo- and (+)-exo-brevicomin viaEnzyme-Mediated Hydrolysis of an Enol Ester , 1990 .
[168] A. Oehlschlager,et al. An example of kinetic resolution by Bakers' yeast: synthesis of enantiomers of endo-brevicomin from the same precursor , 1989 .
[169] J. Chong,et al. Enantioselective syntheses of endo- and exo-brevicomin via α-alkoxystannanes , 1989 .
[170] D. Weisleder,et al. Isolation and structure of rolliniastatin 1 from the South American tree Rollinia mucosa , 1987 .
[171] T. L. Payne,et al. Chiral building units from carbohydrates-XIII. , 1987 .
[172] K. Mori,et al. Synthesis of both the enantiomers of endo-brevicomin, the aggregation pheromone of Dryocoetes autographus , 1985 .
[173] S. Hatakeyama,et al. Preparation of (2R,3S)-1,2-epoxypent-4-en-3-ol, a new chiral building block for the synthesis of (+)-endo- and (–)-exo-brevicomin , 1985 .
[174] Yuichi Kobayashi,et al. Stereocontrolled synthesis of four possible stereoisomers of vicinal diol derivatives via relative 1,2-asymmetric induction. Preparation of optically active exo- and endo-brevicomin , 1985 .
[175] C. Fuganti,et al. On the steric course of addition of Grignard reagents onto α,β-dialkoxy erythro and threo chiral aldehydes. Synthesis of (+) and (−)-exo and endo-brevicomin , 1981 .
[176] A. Meyers. ASYMMETRIC CARBON‐CARBON BOND FORMING REACTIONS , 1979 .
[177] T. J. Katz,et al. The stereochemistry of the olefin metathesis reaction , 1977 .
[178] C. Henrick. The synthesis of insect sex phermones , 1977 .
[179] W. Rojahn,et al. Die permanganatoxydation von 1,5-dienverbindungen , 1965 .
[180] C. Glaser. Beiträge zur Kenntniss des Acetenylbenzols , 1869 .