D. Candito

发表

Harnessing a p-Quinone Methide Intermediate in the Biomimetic Total Synthesis of the Highly Active Antibiotic 20-Deoxy-Elansolid B1.

A. Kirschning, R. Müller, J. Herrmann, 2017, Chemistry.

Synthetic Studies Probing Elansolid Biosynthesis: A para‐Quinone‐Methide‐Triggered Intramolecular Diels–Alder Reaction

A. Kirschning, G. Dräger, Liang-Liang Wang, 2017 .

Discovery of Diaminopyrimidine Carboxamide HPK1 Inhibitors as Preclinical Immunotherapy Tool Compounds.

X. Fradera, Haiyan Xu, M. Bittinger, 2021, ACS medicinal chemistry letters.

Development of an intramolecular aryne ene reaction and application to the formal synthesis of (±)-crinine.

M. Lautens, D. Candito, D. Dobrovolsky, 2012, Journal of the American Chemical Society.

Intramolecular aryne-ene reaction: synthetic and mechanistic studies.

M. Lautens, J. Panteleev, D. Candito, 2011, Journal of the American Chemical Society.

Lessons from the synthetic chemist nature.

A. Kirschning, Gerrit Jürjens, D. Candito, 2015, Natural product reports.

Exploiting the divergent reactivity of aryl-palladium intermediates for the rapid assembly of fluorene and phenanthrene derivatives.

Brian Mariampillai, M. Lautens, B. Laleu, 2009, Angewandte Chemie.

Formal synthesis of nitidine and NK109 via palladium-catalyzed domino direct arylation/N-arylation of aryl triflates.

M. Lautens, D. Candito, Mathieu Blanchot, 2011, Organic letters.

Palladium-catalyzed domino direct arylation/N-arylation: convenient synthesis of phenanthridines.

M. Lautens, D. Candito, 2009, Angewandte Chemie.

Exploiting the chemistry of strained rings: synthesis of indoles via domino reaction of aryl iodides with 2H-azirines.

M. Lautens, D. Candito, 2010, Organic letters.

Palladium-catalyzed reductive ortho-arylation: evidence for the decomposition of 1,2-dimethoxyethane and subsequent arylpalladium(II) reduction.

M. Lautens, Andrew Martins, D. Candito, 2010, Organic letters.

SYNTHESIS OF (S,S)-DIISOPROPYL TARTRATE (E)-CROTYLBORONATE AND ITS REACTION WITH ALDEHYDES: (2R,3R,4R)-1,2-DIDEOXY-2-ETHENYL-4,5-O-(1-METHYLETHYLIDENE)-XYLITOL.

W. Roush, M. Lautens, D. Candito, 2012, Organic syntheses; an annual publication of satisfactory methods for the preparation of organic chemicals.

High yielding alkylations of unactivated sp3 and sp2 centres with alkyl-9-BBN reagents using an NHC-based catalyst: Pd-PEPPSI-IPrf.

Cory Valente, M. Organ, D. Candito, 2008, Chemical communications.

Exploiting the Divergent Reactivity of Aryl—Palladium Intermediates for the Rapid Assembly of Fluorene and Phenanthrene Derivatives.

Brian Mariampillai, M. Lautens, B. Laleu, 2009 .

A Bio-Chemosynthetic Approach to Superparamagnetic Iron Oxide-Ansamitocin Conjugates for Use in Magnetic Drug Targeting.

A. Balakrishnan, M. Ott, A. Kirschning, 2017, Chemistry.

Racemic Synthesis of a Key 1,4-Dihydro-2H-spiro[isoquinoline-3,4′-piperidin]-3′-ol Building Block

Leo A. Joyce, Theodore A. Martinot, Matthew L. Maddess, 2022, Organic Process Research & Development.

Discovery and Optimization of Potent, Selective, and Brain-Penetrant 1-Heteroaryl-1H-Indazole LRRK2 Kinase Inhibitors for the Treatment of Parkinson's Disease.

Theodore A. Martinot, Michael J. Ardolino, Matthew L. Maddess, 2022, Journal of medicinal chemistry.

Development of a Flexible and Robust Synthesis of Tetrahydrofuro[3,4-b]furan Nucleoside Analogues.

Ryan V. Quiroz, Hongming Li, D. Witter, 2021, The Journal of organic chemistry.