2.09 The Aldol Reaction: Group IV Enolates (Mukaiyama, Enol Ethers)
S. Kobayashi,* Y. Yamashita, W. J. Yoo, T. Kitanosono, J. -F. Soulé. Vol. Comprehensive Organic Synthesis II (Second Edition), Comprehensive Organic Synthesis II (Second Edition) ed., Elsevier, Amsterdam Elsevier, 2014, 396-450.  Link
9.ga
A Simple and Efficient Synthesis of (Hetero)Aryl-Substituted Benzothiazolyl or Benzoxazolyl Furan, Thiophene and N-methylpyrrole Derivatives through a Palladium-Catalyzed Regioselective C–H Bond Arylation
F. Abdellaoui, C. Youssef, H. Ben Ammar, J.-F. Soulé, H. Doucet* . Synthesis 2014, 46, 3341-3350. (DOI:10.1055/s-0034-1379021).  Link
94.ticlopidine
A Straightforward One‐Step Access to Ticlopidine Derivatives Arylated at the C5‐Position of the Thienyl Ring via Pd‐Catalyzed Direct Arylations
D. Atoui, H. Li, R. Ben Salem, T. Roisnel, J.-F. Soulé,* H. Doucet* . Asian J. Org. Chem. 2019, 8, 2155-2161. (10.1002/ajoc.201900609).  Link
56.selenophenereview2
Access to (Hetero)arylated Selenophenes via Palladium-catalysed Stille, Negishi or Suzuki Couplings or C−H Bond Functionalization Reaction
A. Skhiri, R. Ben Salem, J.-F. Soulé,* H. Doucet* . ChemCatChem 2017, 9, 2895-2913. (DOI:10.1002/cctc.201700256) Review.  Link
78.radical cyclization–asc
Access to 3-(2-Oxoalkyl)-azaspiro[4.5]trienones via Acid-Triggered Oxidative Cascade Reactions through Alkenyl Peroxide Radical Intermediate
C.-S. Wang, T. Roisnel, P. H. Dixneuf, J.-F. Soulé* . Adv. Synth. Catal. 2019, 361, 445-450. (10.1002/adsc.201801203).  Link
107.cc wided pcpt
Access to Functionalized Luminescent Pt(II) Complexes by Photoredox-Catalyzed Minisci Alkylation of 6-Aryl-2,2’-bipyridines
W. Hagui, M. Cordier, J. Boixel,* J.-F. Soulé*. Chem. Commun.  2021, 57, 1038-1041. (10.1039/D0CC07307E).  Link
Acridinium-based photoredox catalysts, synthesis and use thereof in oxidative cleavage of C–O bonds
Y.-X. Cao, G. Zhu, J.-F. Soulé*. EP 20306217.9 .
47.cc 2017
An unexpected copper-catalyzed carbonylative acetylation of amines
Y. Li, C. Wang, F. Zhu, Z. Wang, J.-F. Soulé, P. H. Dixneuf, X.-F. Wu* . Chem. Commun. 2017, 53, 142-144. (DOI:10.1039/C6CC08929A).  Link
89.ga chem pah
Application of Palladium-Catalyzed C(sp2)–H Bond Arylation to the Synthesis of Polycyclic (Hetero)Aromatics
W. Hagui, H. Doucet, J.-F. Soulé* . Chem. 2019, 5, 2006-2078. (10.1016/j.chempr.2019.06.005) Review.  Link
40.ejic201600675 toc 0001 m
Asymmetrical 1,3-Bis(heteroazolyl)benzene Platinum Complexes with Tunable Second-Order Non-Linear Optical Properties
T. T. Dang, J.-F. Soulé, H. Doucet, M. A. Benmensour, A. Boucekkine, A. Colombo,* C. Dragonetti, S. Righetto, D. Jacquemin, J. Boixel,* V. Guerchais. Eur. J. Inorg. Chem. 2016, 4774-4782. (DOI:10.1002/ejic.201600675).  Link
10.i t0227 ga 10 1055 s 0033 1340188
Benzenesulfonyl Chlorides: Alternative Coupling Partners for Regiocontrolled Palladium-Catalyzed Direct Desulfitative 5-Arylation of Furans
A. Beladhria, K. Yuan, H. Ben Ammar, J.-F. Soulé, R. Ben Salem, H. Doucet* . Synthesis 2014, 46, 2515-2523. (DOI:10.1055/s-0033-1340188).  Link
110.ga cd3 2
Broadening of Horizons in the Synthesis of CD3-Labeled Molecules” Review Selected as Inside Cover
Q. Sun, J.-F. Soulé*. Chem. Soc. Rev.  2021, 50, 10806-10835. (10.1039/D1CS00544H).  Link
104.beta pyrazole3
C−H Bond Arylation of Pyrazoles at the β-Position: General Conditions and Computational Elucidation for a High Regioselectivity
X. Shi, E. D. Sosa Carrizo, M. Cordier, J. Roger, N. Pirio, J.-C. Hierso, P. Fleurat-Lessard,* J.-F. Soulé,* H. Doucet*. Chem. Eur. J.  2021, 27, 5546-5554 (10.1002/chem.202100031).  Link
82.acs–iridium rev2
Catalyst-Controlled Regiodivergent C–H Arylation Site of Fluorinated 2-Arylpyridine Derivatives: Application to Luminescent Iridium(III) Complexes
R. Boyaala, R. Touzani, T. Roisnel, V. Dorcet, E. Caytan, D. Jacquemin,* J. Boixel, V. Guerchais,* H. Doucet,* J.-F. Soulé*. ACS Catal. 2019, 9, 1320-1328. (10.1021/acscatal.8b04553).  Link
18.toc mariemrev
Conditions for palladium-catalyzed direct arylations of 4-bromo and 4-iodo N-substituted pyrazoles without C-Br or C-I bond cleavage
M. Brahim, I. Smari, H. Ben Ammar,* B. Ben Hassine, J.-F. Soulé, H. Doucet* . Org. Chem. Front. 2015, 2, 917-926. (DOI:10.1039/C5QO00093A).  Link