J. D. Hartog

发表

Solid-phase synthesis of peptidosulfonamide containing peptides derived from Leu-enkephalin

R. Liskamp, D. B. Bont, G.W.H. Dijkstra, 1996 .

A straightforward synthesis of 1,3-dichloro-5,8-dihydroisoquinoline by consecutive Stille cross-coupling and metathesis reactions

A. V. D. Hoogenband, J. Terpstra, J. D. Hartog, 2009 .

An efficient one-pot synthesis of novel 4-aryl-1-methyloxindoles

J. Lange, A. V. D. Hoogenband, J. Terpstra, 2006 .

Solid phase ring-closing metathesis: Cyclization/cleavage approach towards a seven membered cycloolefin

G. M. Visser, J. Maarseveen, J. D. Hartog, 1996 .

Synthesis of oligoribonucleotides with sequences identical to the nucleation region of Tobacco Mosaic Virus RNA: Preparation of AAG, AAGAAG and AAGAAGUUG via phosphotriester methods†

J. V. Boom, G. Wille, J. D. Hartog, 2010 .

The preparation of diribonucleoside monophosphates containing 4-thiouridine via the phosphotriester approach

J. H. Boom, G. A. Marel, J. D. Hartog, 1976 .

A novel synthesis of N-(piperidin-4-yl)-1,3-dihydroindol-2-one via an intramolecular Pd-catalyzed amination

J. Lange, A. V. D. Hoogenband, J. Terpstra, 2004 .

An efficient synthesis of 4-bromo-N-substituted oxindoles by an intramolecular copper-catalyzed amidation reaction

J. Lange, A. V. D. Hoogenband, J. Terpstra, 2007 .

Synthesis of 5-deazaflavine adenine dinucleotide (5-dFAD) by a modified triester approach

J. H. Boom, H. Plas, G. A. Marel, 2010 .

4-Nitrophenyl 4-morpholinylphosphonochloridate: A convenient reagent for the synthesis of ribonucleoside mono-, di- and tri-phosphates

J. H. Boom, J. D. Hartog, 2010 .

Chemical synthesis of pppA2'p5'A2'p5'A, an interferon-induced inhibitor of protein synthesis, and some functional analogs

J. H. Boom, R. Crea, R. Wijnands, 1981 .

Chemical synthesis of a 5′‐ and 3′/2′‐phosphorylated heptamer sequence of E. coli tRNA fmet: pAGCCUGG(3′/2′)p via phosphotriester methods

J. H. Boom, J. D. Hartog, 2010 .

Synthesis of the 5′‐triphosphate of a trimer containing 2′‐5′‐internucleotide linked riboadenosines

J. H. Boom, R. Crea, J. D. Hartog, 2010 .

Purification of fully protected oligonucleotide phosphotriester intermediates by gel filtration on sephadex LH-60

J. H. Boom, G. A. Marel, R. Arentzen, 1979 .

Two novel syntheses of the histamine H3 antagonist thioperamide

J. Lange, A. V. D. Hoogenband, J. D. Hartog, 1995 .

New methods for the synthesis of 2-arylpyrroles

J. Bouw, J. D. Hartog, C. Kruse, 1987 .

Synthesis of 5-deazaflavin adenine dinucleotide (5-dFAD) using a modified triester approach.

J. H. Boom, H. Plas, G. A. Marel, 2010 .

Structure-Activity Studies on the Corticotropin Releasing Factor Antagonist Astressin, Minimal Sequence Necessary for Antagonistic Activity: Implications for a New Pharmacophoric Model

R. Liskamp, D. Rijkers, J. D. Hartog, 2001 .