Expanding the Medicinal Chemist Toolbox: Comparing Seven C(sp2)–C(sp3) Cross-Coupling Methods by Library Synthesis AW Dombrowski, NJ Gesmundo, AL Aguirre, KA Sarris, JM Young, ... ACS Medicinal Chemistry Letters 11 (4), 597-604, 2020 | 179 | 2020 |
Functionalized 4-carboxy-and 4-keto-2, 3-dihydropyrroles via Ni (II)-catalyzed nucleophilic amine ring-opening cyclizations of cyclopropanes MC Martin, DV Patil, S France The Journal of Organic Chemistry 79 (7), 3030-3039, 2014 | 105 | 2014 |
Going beyond Polycomb: EZH2 functions in prostate cancer SH Park, KW Fong, E Mong, MC Martin, GE Schiltz, J Yu Oncogene 40 (39), 5788-5798, 2021 | 74 | 2021 |
A Catalytic Diastereoselective Formal [5+ 2] Cycloaddition Approach to Azepino [1, 2‐a] indoles: Putative Donor–Acceptor Cyclobutanes as Reactive Intermediates R Shenje, MC Martin, S France Angewandte Chemie International Edition 53 (50), 13907-13911, 2014 | 74 | 2014 |
Getting the Big Picture E Balka Methods of information in medicine 42 (04), 324-330, 2003 | 59 | 2003 |
Small molecule approaches for targeting the polycomb repressive complex 2 (PRC2) in cancer MC Martin, G Zeng, J Yu, GE Schiltz Journal of Medicinal Chemistry 63 (24), 15344-15370, 2020 | 45 | 2020 |
The Catalytic, Formal Homo‐Nazarov Cyclization as a Template for Diversity‐Oriented Synthesis MC Martin≠, R Shenje≠, S France Israel Journal of Chemistry 56 (6-7), 499-511, 2016 | 39 | 2016 |
Calcium-Catalyzed Formal [5 + 2] Cycloadditions of Alkylidene β-Ketoesters with Olefins: Chemodivergent Synthesis of Highly Functionalized Cyclohepta[b]indole … AN Parker, MC Martin, R Shenje, S France Organic letters 21 (18), 7268-7273, 2019 | 31 | 2019 |
Versatile methods to dispense submilligram quantities of solids using chemical-coated beads for high-throughput experimentation MC Martin, GM Goshu, JR Hartnell, CD Morris, Y Wang, NP Tu Organic Process Research & Development 23 (9), 1900-1907, 2019 | 25 | 2019 |
Dehydrative Nazarov-type electrocyclizations of alkenyl (hetero) aryl carbinols via calcium catalysis: Access to cyclopenta [b] thiophenes and indene derivatives MC Martin, MJ Sandridge, CW Williams, ZA Francis, S France Tetrahedron 73 (29), 4093-4108, 2017 | 14 | 2017 |
Calcium-catalyzed formal [5+ 2] cycloaddition of alkylidene beta-ketoesters with substituted olefins: Chemodivergent synthesis of highly functionalized cyclohepta [b] indoles A Parker, M Martin, R Shenje, S France ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 258, 2019 | | 2019 |
Catalytic formal [5+ 2] cycloaddition approach to azepino [1, 2-a] indoles and cyclohepta [b] indoles MC Martin, R Shenje, S France ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 250, 2015 | | 2015 |
Catalytic, diastereoselective synthesis of azepino [1, 2-a] indoles via formal [5+ 2] cycloadditions of N-indolyl alkylidene beta-amide esters and alkenes: Putative donor … R Shenje, MC Martin, SA France ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 248, 2014 | | 2014 |
Catalytic and diastereoselective synthesis of benzo-and heteroaryl fused cycloheptyl rings via formal [5+ 2] cycloadditions of alkylidene beta-keto esters and alkenes MC Martin, R Shenje, S France ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 248, 2014 | | 2014 |
Study of percutaneous absorption of all-trans-retinoic acid with three galenic formulations. C Boutrand, JL Michel, MC Martin, L Misery, F Cambazard JOURNAL OF INVESTIGATIVE DERMATOLOGY 112 (1), 133-133, 1999 | | 1999 |
Supporting Information For Calcium-Catalyzed Formal [5+ 2] Cycloadditions of Alkylidene β-Ketoesters with Olefins: Chemodivergent Synthesis of Highly Functionalized Cyclohepta … AN Parker, MC Martin, R Shenje, S France | | |
Correction to Lancet Healthy Longev 2021; 2: e121–22 JP Michel, M Leonardi, M Martin, M Prina | | |