Discussion Addendum for: Ring-closing Metathesis Synthesis of N-Boc-3-pyrroline

[1]  W. R. Jackson,et al.  Ring-closing Metathesis in Peptides – the Sting is in the Tail! , 2011 .

[2]  G. Verdine,et al.  Synthesis of all-hydrocarbon stapled α-helical peptides by ring-closing olefin metathesis , 2011, Nature Protocols.

[3]  I. Markó,et al.  Studies towards the Synthesis of Pentalenene: Mechanistic Insights into the Isomerization Phenomenon During RCM of Medium‐Sized Rings , 2011 .

[4]  J. Wade,et al.  Synthesis, conformational analysis and biological properties of a dicarba derivative of the antimicrobial peptide, brevinin-1BYa , 2011, European Biophysics Journal.

[5]  Andrew B. Mahon,et al.  Solid-phase synthesis of short α-helices stabilized by the hydrogen bond surrogate approach , 2010, Nature Protocols.

[6]  Richard L. Pederson,et al.  Low catalyst loadings in olefin metathesis: synthesis of nitrogen heterocycles by ring-closing metathesis. , 2010, Organic letters.

[7]  I. R. Morgan,et al.  A simple oxidative procedure for the removal of ruthenium residues from metathesis reaction products , 2010 .

[8]  Brian D. Doan,et al.  Large-scale synthesis of SB-462795, a cathepsin K inhibitor: the RCM-based approaches , 2009 .

[9]  M. Campbell,et al.  Asymmetric synthesis of (+)-polyanthellin A. , 2009, Journal of the American Chemical Society.

[10]  Xudong Wei,et al.  Second-Generation Process for the HCV Protease Inhibitor BILN 2061: A Greener Approach to Ru-Catalyzed Ring-Closing Metathesis† , 2009 .

[11]  Gregory W. Stockdale,et al.  Development of a Robust Ring-Closing Metathesis Reaction in the Synthesis of SB-462795, a Cathepsin K Inhibitor , 2008 .

[12]  Xudong Wei,et al.  RCM macrocyclization made practical: an efficient synthesis of HCV protease inhibitor BILN 2061. , 2008, Organic letters.

[13]  Roger A. Sheldon,et al.  The E Factor: fifteen years on , 2007 .

[14]  A. Kirschning,et al.  Sustainable concepts in olefin metathesis. , 2007, Angewandte Chemie.

[15]  C. Toniolo,et al.  Facile and E-selective intramolecular ring-closing metathesis reactions in 3(10)-helical peptides: a 3D structural study. , 2007, Journal of the American Chemical Society.

[16]  S. Arseniyadis,et al.  Cross-Metathesis between α-Methylene-γ-butyrolactone and Olefins: A Dramatic Additive Effect , 2007 .

[17]  Steven H. Szczepankiewicz,et al.  A rapid and simple cleanup procedure for metathesis reactions. , 2007, Organic letters.

[18]  J. Steinke,et al.  Phenylphosphoric Acid as a New Additive to Inhibit Olefin Isomerisation in Ruthenium‐Catalysed Metathesis Reactions , 2007 .

[19]  J. L. Snelgrove,et al.  Oligomers as intermediates in ring-closing metathesis. , 2007, Journal of the American Chemical Society.

[20]  C. Senanayake,et al.  Epimerization reaction of a substituted vinylcyclopropane catalyzed by ruthenium carbenes: mechanistic analysis. , 2006, The Journal of organic chemistry.

[21]  Xudong Wei,et al.  Efficient large-scale synthesis of BILN 2061, a potent HCV protease inhibitor, by a convergent approach based on ring-closing metathesis. , 2006, The Journal of organic chemistry.

[22]  C. Crudden,et al.  Functionalized mesoporous silicates for the removal of ruthenium from reaction mixtures. , 2006, Organic letters.

[23]  S. LaPlante,et al.  RCM of tripeptide dienes containing a chiral vinylcyclopropane moiety: impact of different Ru-based catalysts on the stereochemical integrity of the macrocyclic products. , 2005, The Journal of organic chemistry.

[24]  R. Grubbs,et al.  Prevention of undesirable isomerization during olefin metathesis. , 2005, Journal of the American Chemical Society.

[25]  Thomas Nicola,et al.  First Scale-Up to Production Scale of a Ring Closing Metathesis Reaction Forming a 15-Membered Macrocycle as a Precursor of an Active Pharmaceutical Ingredient , 2005 .

[26]  W. Xiao,et al.  Lewis acid assisted ring-closing metathesis of chiral diallylamines: an efficient approach to enantiopure pyrrolidine derivatives. , 2005, Organic letters.

[27]  J. Winkler,et al.  Metathesis approach to the synthesis of polyheterocyclic structures from oxanorbornenes. , 2004, Organic letters.

[28]  B. Schmidt Catalysis at the Interface of Ruthenium Carbene and Ruthenium Hydride Chemistry: Organometallic Aspects and Applications to Organic Synthesis , 2004 .

[29]  B. Alcaide,et al.  Ruthenium-catalyzed chemoselective N-allyl cleavage: novel Grubbs carbene mediated deprotection of allylic amines. , 2003, Chemistry.

[30]  R. Grubbs Handbook of metathesis , 2003 .

[31]  B. Schmidt An Olefin Metathesis/Double Bond Isomerization Sequence Catalyzed by an In Situ Generated Ruthenium Hydride Species , 2003 .

[32]  B. Kim,et al.  An efficient method for removal of ruthenium byproducts from olefin metathesis reactions. , 2003, Organic letters.

[33]  Richard L. Pederson,et al.  Applications of Olefin Cross Metathesis to Commercial Products , 2002 .

[34]  C. Cadot,et al.  Olefin isomerization by a ruthenium carbenoid complex. Cleavage of allyl and homoallyl groups , 2002 .

[35]  S. Nolan,et al.  The Cl2(PCy3)(IMes)Ru(CHPh) catalyst: olefin metathesis versus olefin isomerization , 2002 .

[36]  R. Grubbs,et al.  Ring-closing metathesis of olefinic peptides: design, synthesis, and structural characterization of macrocyclic helical peptides. , 2001, The Journal of organic chemistry.

[37]  U. Kazmaier,et al.  A Short and Efficient Synthesis of (S)-1-Boc-2,5-dihydro-1H-pyrrole-2-carboxylic Acid , 2001 .

[38]  G. Georg,et al.  A convenient method for the efficient removal of ruthenium byproducts generated during olefin metathesis reactions. , 2001, Organic letters.

[39]  Paquette,et al.  A convenient method for removing all highly-colored byproducts generated during olefin metathesis reactions , 2000, Organic letters.

[40]  Nolan,et al.  Ruthenium carbene complexes with N,N'-bis(mesityl)imidazol-2-ylidene ligands: RCM catalysts of extended scope , 2000, The Journal of organic chemistry.

[41]  T. Hoye,et al.  Some allylic substituent effects in ring-closing metathesis reactions: allylic alcohol activation. , 1999, Organic letters.

[42]  R. Grubbs,et al.  Purification technique for the removal of ruthenium from olefin metathesis reaction products , 1999 .

[43]  John A. Tallarico,et al.  New Reactivity from (PCy3)2Cl2RuCHPh: A Mild Catalyst for Kharasch Additions , 1999 .

[44]  Helen E Blackwell,et al.  Highly Efficient Synthesis of Covalently Cross-Linked Peptide Helices by Ring-Closing Metathesis. , 1998, Angewandte Chemie.

[45]  A. Fürstner,et al.  Total Syntheses of (+)-Ricinelaidic Acid Lactone and of (−)-Gloeosporone Based on Transition-Metal-Catalyzed C−C Bond Formations , 1997 .

[46]  Scott J. Miller,et al.  Application of Ring-Closing Metathesis to the Synthesis of Rigidified Amino Acids and Peptides , 1996 .

[47]  Scott J. Miller,et al.  Catalytic Ring-Closing Metathesis of Dienes: Application to the Synthesis of Eight-Membered Rings , 1995 .