Formal total synthesis of Palmerolide A

[1]  D. Mohapatra,et al.  Synthesis of the C1–C15 fragment of palmerolide A via protecting group dependent RCM reaction , 2013 .

[2]  David M. Jones,et al.  Formal synthesis of palmerolide A, featuring alkynogenic fragmentation and syn-selective vinylogous aldol chemistry. , 2013, Organic letters.

[3]  J. Campagne,et al.  Update 1 of: macrolactonizations in the total synthesis of natural products. , 2013, Chemical reviews.

[4]  K. Prasad,et al.  Formal total synthesis of palmerolide A. , 2012, Chemistry.

[5]  T. Loh,et al.  Palladium-catalyzed cross-coupling of unactivated alkenes with acrylates: application to the synthesis of the C13-C21 fragment of palmerolide A. , 2012, Chemistry.

[6]  K. Kaliappan,et al.  A Shimizu non-aldol approach to the formal total synthesis of palmerolide A. , 2011, Chemistry, an Asian journal.

[7]  J. Yadav,et al.  Ring-closing metathesis (RCM) based synthesis of the macrolactone core of amphidinolactone A. , 2011, Organic & biomolecular chemistry.

[8]  K. Prasad,et al.  Enantioselective formal synthesis of palmerolide A. , 2011, Organic letters.

[9]  J. Yadav,et al.  Total synthesis of Z-isomer of phomolide B , 2011 .

[10]  K. Kaliappan,et al.  A formal total synthesis of palmerolide A. , 2010, Chemistry.

[11]  K. Prasad,et al.  Stereoselective Synthesis of C1-C18 Region of Palmerolide A from Tartaric Acid , 2010 .

[12]  Jun Li,et al.  Stereoselective total synthesis of etnangien and etnangien methyl ester. , 2010, The Journal of organic chemistry.

[13]  B. Baker,et al.  Synthesis of the C3–14 fragment of palmerolide A using a chiral pool based strategy , 2010 .

[14]  G. N. Sastry,et al.  Total syntheses and absolute stereochemistry of decarestrictines C1 and C2 , 2009 .

[15]  D. Hall,et al.  Catalytic asymmetric synthesis of palmerolide A via organoboron methodology. , 2009, Journal of the American Chemical Society.

[16]  Jun Li,et al.  Modular total synthesis of archazolid A and B. , 2009, The Journal of organic chemistry.

[17]  Jun Li,et al.  Total synthesis of etnangien. , 2009, Journal of the American Chemical Society.

[18]  R. SanMartin,et al.  Divergent synthesis of isoindolo[2,1-a]indole and indolo[1,2-a]indole through copper-catalysed C- and N-arylations , 2009 .

[19]  Ya‐Ping Sun,et al.  Chemical synthesis and biological evaluation of palmerolide A analogues. , 2008, Journal of the American Chemical Society.

[20]  R. Hsung,et al.  Synthesis of the C1-C23 fragment of Spirastrellolide A. , 2008, Organic letters.

[21]  Ya‐Ping Sun,et al.  Total synthesis of the originally proposed and revised structures of palmerolide A and isomers thereof. , 2008, Journal of the American Chemical Society.

[22]  M. Maier,et al.  A concise route to the C3–C23 fragment of the macrolide palmerolide A , 2007 .

[23]  B. Baker,et al.  On the stereochemistry of palmerolide A , 2007 .

[24]  S. Chandrasekhar,et al.  Towards the synthesis of Palmerolide A: asymmetric synthesis of C1–C14 fragment , 2007 .

[25]  J. Yadav,et al.  A convergent approach for the total synthesis of (−)-synrotolide diacetate , 2007 .

[26]  K C Nicolaou,et al.  Total synthesis of the originally proposed and revised structures of palmerolide A. , 2007, Angewandte Chemie.

[27]  K. Kaliappan,et al.  Synthetic Studies on a Marine Natural Product, Palmerolide A: Synthesis of C1-C9 and C15-C21 Fragments , 2007 .

[28]  S. Lebreton,et al.  Total synthesis and structure revision of the marine metabolite palmerolide A. , 2007, Journal of the American Chemical Society.

[29]  D. Trauner,et al.  Total synthesis of (-)-archazolid B. , 2007, Journal of the American Chemical Society.

[30]  R. Grubbs,et al.  Protecting group directed ring-closing metathesis (RCM): the first total synthesis of an anti-malarial nonenolide , 2007 .

[31]  J. Palenzuela,et al.  Synthesis of 2,5-disubstituted octahydroquinolin-4-ones via anintramolecular hetero Diels-Alder reaction. , 2007, Molecules.

[32]  E. Negishi Transition Metal-Catalyzed Organometallic Reactions that Have Revolutionized Organic Synthesis , 2007 .

[33]  A. Gradillas,et al.  Macrocyclization by ring-closing metathesis in the total synthesis of natural products: reaction conditions and limitations. , 2006, Angewandte Chemie.

[34]  S. Danishefsky,et al.  Small molecule natural products in the discovery of therapeutic agents: the synthesis connection. , 2006, The Journal of organic chemistry.

[35]  C. Amsler,et al.  Palmerolide A, a cytotoxic macrolide from the antarctic tunicate Synoicum adareanum. , 2006, Journal of the American Chemical Society.

[36]  R. Sagar,et al.  Reductive opening of glycal derived highly functionalized 2,3-epoxy-1-iodides with zinc dust: an efficient method for the synthesis of acyclic long chain polyhydroxylated terminal alkenic alcohols , 2006 .

[37]  M. Roth,et al.  Salicylihalamide A Inhibits the V0 Sector of the V-ATPase through a Mechanism Distinct from Bafilomycin A1* , 2004, Journal of Biological Chemistry.

[38]  Alexander Deiters,et al.  Synthesis of oxygen- and nitrogen-containing heterocycles by ring-closing metathesis. , 2004, Chemical reviews.

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

[40]  J. Prunet Recent methods for the synthesis of (E)-alkene units in macrocyclic natural products. , 2003, Angewandte Chemie.

[41]  M. Christmann,et al.  The first total synthesis of +-ratjadone. , 2001, The Journal of organic chemistry.

[42]  R. Grubbs,et al.  The development of L2X2Ru=CHR olefin metathesis catalysts: an organometallic success story. , 2001, Accounts of chemical research.

[43]  Y. Al-Abed,et al.  Studies directed toward the synthesis of carba-D-arabinofuranose , 2000 .

[44]  A. Fürstner Olefin Metathesis and Beyond , 2000 .

[45]  Maier Synthesis of Medium-Sized Rings by the Ring-Closing Metathesis Reaction. , 2000, Angewandte Chemie.

[46]  K. Nacro,et al.  Attempt to rationalize the diastereoselectivity in the addition of ester enolate to optically active α,β-epoxyaldehydes , 1999 .

[47]  S. Armstrong Ring closing diene metathesis in organic synthesis , 1998 .

[48]  Robert H. Grubbs,et al.  Recent advances in olefin metathesis and its application in organic synthesis , 1998 .

[49]  J. Tanaka,et al.  Bioactive marine macrolides , 1998 .

[50]  I. Paterson,et al.  Total Synthesis of Bioactive Marine Macrolides , 1995 .

[51]  M. VanNieuwenhze,et al.  Catalytic Asymmetric Dihydroxylation , 1994 .

[52]  M. Frigerio,et al.  A mild oxidizing reagent for alcohols and 1,2-diols: o-iodoxybenzoic acid (IBX) in DMSO , 1994 .

[53]  D. Dess,et al.  A useful 12-I-5 triacetoxyperiodinane (the Dess-Martin periodinane) for the selective oxidation of primary or secondary alcohols and a variety of related 12-I-5 species , 1991 .

[54]  K. Sharpless,et al.  Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization , 1987 .

[55]  K. Takai,et al.  Simple and selective method for RCHO → (E)-RCH=CHX conversion by means of a CHX3-CrCl2 system , 1986 .

[56]  E. Dalcanale,et al.  Selective oxidation of aldehydes to carboxylic acids with sodium chlorite-hydrogen peroxide , 1986 .

[57]  K. Horita,et al.  On the selectivity of deprotection of benzyl, mpm (4-methoxybenzyl) and dmpm (3,4-dimethoxybenzyl) protecting groups for hydroxy functions , 1986 .

[58]  D. Dess,et al.  Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones , 1983 .

[59]  S. Nozaki,et al.  Rapid Peptide Synthesis in Liquid Phase. Preparation of Angiotensin II and Delta-sleep-inducing Peptide by the “Hold-in-Solution” Method , 1982 .

[60]  A. Pfaltz,et al.  Regioselective Opening of α‐ and β‐Alkoxyepoxides with Trimethylaluminum , 1982 .

[61]  I. T. Ibrahim,et al.  Carbodiimide chemistry: recent advances , 1981 .

[62]  W. Childers,et al.  Oxidation of α,β-un saturated aldehydes , 1981 .

[63]  Marian Mikoz.xl,et al.  Recent developments in the carbodiimide chemistry , 1981 .

[64]  T. Katsuki,et al.  A rapid esterification by means of mixed anhydride and its application to large-ring lactonization. , 1979 .

[65]  W. Steglich,et al.  Simple Method for the Esterification of Carboxylic Acids , 1978 .

[66]  C. Brown,et al.  “P-2 nickel” catalyst with ethylenediamine, a novel system for highly stereospecific reduction of alkynes to cis-olefins , 1973 .

[67]  J. Preston,et al.  A RAPID SYNTHESIS OF OLIGOPEPTIDE DERIVATIVES WITHOUT ISOLATION OF INTERMEDIATES. , 1965, Journal of the American Chemical Society.