Published in J Am Chem Soc on April 28, 2004
Chemistry of polyvalent iodine. Chem Rev (2008) 2.13
Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach. J Am Chem Soc (2008) 2.10
Allene formation by gold catalyzed cross-coupling of masked carbenes and vinylidenes. Proc Natl Acad Sci U S A (2007) 1.37
Cu-catalyzed cross-dehydrogenative coupling: a versatile strategy for C-C bond formations via the oxidative activation of sp(3) C-H bonds. Proc Natl Acad Sci U S A (2006) 1.30
Enantioselective total syntheses of (-)-palau'amine, (-)-axinellamines, and (-)-massadines. J Am Chem Soc (2011) 1.25
The essence of total synthesis. Proc Natl Acad Sci U S A (2004) 0.96
Room-temperature aromatization of tetrahydro-β-carbolines by 2-iodoxybenzoic acid: utility in a total synthesis of eudistomin U. Org Lett (2010) 0.96
Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance. Chem Soc Rev (2012) 0.84
Potassium N-iodo p-toluenesulfonamide (TsNIK, Iodamine-T): a new reagent for the oxidation of hydrazones to diazo compounds. Chemistry (2014) 0.75
An approach towards azafuranomycin analogs by gold-catalyzed cycloisomerization of allenes: synthesis of (αS,2R)-(2,5-dihydro-1H-pyrrol-2-yl)glycine. Beilstein J Org Chem (2013) 0.75
Effect of Substituents and Stability of Transient Aluminum-Aminals in the Presence of Nucleophiles. Synthesis (Stuttg) (2014) 0.75
The Diels--Alder reaction in total synthesis. Angew Chem Int Ed Engl (2002) 5.22
Tandem reactions, cascade sequences, and biomimetic strategies in total synthesis. Chem Commun (Camb) (2003) 1.91
Oxidation of silyl enol ethers by using IBX and IBX.N-oxide complexes: a mild and selective reaction for the synthesis of enones. Angew Chem Int Ed Engl (2002) 1.27
HIO3 and I2O5: mild and selective alternative reagents to IBX for the dehydrogenation of aldehydes and ketones. Angew Chem Int Ed Engl (2002) 1.03
Modulation of the reactivity profile of IBX by ligand complexation: ambient temperature dehydrogenation of aldehydes and ketones to alpha,beta-unsaturated carbonyl compounds. Angew Chem Int Ed Engl (2002) 0.99
The total synthesis of coleophomones B, C, and D. J Am Chem Soc (2005) 0.91
New reactions of IBX: oxidation of nitrogen- and sulfur-containing substrates to afford useful synthetic intermediates. Angew Chem Int Ed Engl (2003) 0.86
Spiroperoxy lactones from furans in one pot: synthesis of (+)-premnalane a. Org Lett (2007) 0.85
Synthesis of imides, N-acyl vinylogous carbamates and ureas, and nitriles by oxidation of amides and amines with Dess-Martin periodinane. Angew Chem Int Ed Engl (2005) 0.83
Regioselective ortho lithiation of 3-aryl and 3-styryl furans. Org Lett (2005) 0.82
The total synthesis of coleophomones B and C. Angew Chem Int Ed Engl (2002) 0.82
Copper(I) complexes of a heavily fluorinated beta-diketiminate ligand: synthesis, electronic properties, and intramolecular aerobic hydroxylation. Inorg Chem (2003) 0.79
Biomimetic total synthesis of litseaverticillols B, E, I, and J and structural reassignment of litseaverticillol E. Org Lett (2004) 0.79
Illustrating the power of singlet oxygen chemistry in a synthetic context: biomimetic syntheses of litseaverticillols A-G, I and J and the structural reassignment of litseaverticillol E. Chemistry (2005) 0.75
Singlet oxygen-mediated synthesis of bis-spiroketals found in azaspiracids. Org Lett (2014) 0.75
Using singlet oxygen to synthesise a [6,6,5]-bis-spiroketal in one-pot from a simple 2,5-disubstituted furan. Org Biomol Chem (2007) 0.75
From simple furans to complex nitrogen-bearing aromatic polycycles by means of a flexible and general reaction sequence initiated by singlet oxygen. Chemistry (2013) 0.75
Photooxidations of 2-(γ,ε-dihydroxyalkyl) furans in water: synthesis of DE-bicycles of the pectenotoxins. Org Lett (2012) 0.75
Gamma-spiroketal gamma-lactones from 2-(gamma-hydroxyalkyl)furans: syntheses of epi-pyrenolide D and crassalactone D. Org Lett (2009) 0.75
Synthesis of the spirocyclic core of the prunolides using a singlet oxygen-mediated cascade sequence. Org Lett (2005) 0.75
A versatile and general one-pot method for synthesizing bis-spiroketal motifs. Org Lett (2006) 0.75
Singlet oxygen initiated cascade transformation of a simple difuran into the key ABC-ring motif of the pectenotoxins. Chem Commun (Camb) (2010) 0.75
A versatile synthesis of Meyers' bicyclic lactams from furans: singlet-oxygen-initiated reaction cascade. Angew Chem Int Ed Engl (2012) 0.75
One-pot synthesis of the tetracyclic framework of the aromatic erythrina alkaloids from simple furans. Org Lett (2013) 0.75
Using singlet oxygen to synthesise the CDE-ring system of the pectenotoxins. Org Biomol Chem (2012) 0.75