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Efficacious N-protection of O-aryl sulfamates with 2,4-dimethoxybenzyl groups. Tristan Reuillon, Annalisa Bertoli, Roger J. Griffin, Duncan C. Miller, Bernard T. Golding , Org. Biomol. Chem. , 2012 , 10 , 7610

Two decades of recent advances of Ugi reactions: synthetic and pharmaceutical applications. Manar Ahmed Fouad, Hamida Abdel-Hamid, Mohammed Salah Ayoup , RSC Adv. , 2020 , 10 , 42644

A fluorescent 3,7-bis-(naphthalen-1-ylethynylated)-2′-deoxyadenosine analogue reports thymidine in complementary DNA by a large emission Stokes shift. Masaki Yanagi, Azusa Suzuki, Robert H. E. Hudson, Yoshio Saito , Org. Biomol. Chem. , 2018 , 16 , 1496

Divergent synthesis of 4-amino indoles with free amine groups via tandem reaction of 2-alkynylanilines. Xiaohua Li, Qiuqin He, Renhua Fan , Org. Chem. Front. , 2022 , 9 , 4146

Synthesis of 4′-aminopantetheine and derivatives to probe aminoglycoside N-6′-acetyltransferase. Xuxu Yan, T. Olukayode Akinnusi, Aaron T. Larsen, Karine Auclair , Org. Biomol. Chem. , 2011 , 9 , 1538

Synthesis of the fungus metabolite cladosin C. David Linder, Rainer Schobert , Org. Biomol. Chem. , 2017 , 15 , 7672

Recent applications of multicomponent reactions in medicinal chemistry. Paul Slobbe, Eelco Ruijter, Romano V. A. Orru , Med. Chem. Commun. , 2012 , 3 , 1189

Synthesis of γ-lactam analogues of carbapenems with substituted-thio groups at the C-3 position. Shohei Hashiguchi, Hideaki Natsugari, Michihiko Ochiai , J. Chem. Soc., Perkin Trans. 1 , 1988 , 2345

Chiral β3-isocyanopropionates for multicomponent synthesis of peptides and depsipeptides containing a β-amino acid fragment. Danil P. Zarezin, Olga I. Shmatova, Valentine G. Nenajdenko , Org. Biomol. Chem. , 2018 , 16 , 5987

Synthesis of new betulinic acid–peptide conjugates and in vivo and in silico studies of the influence of peptide moieties on the triterpenoid core activity. Anastasiya I. Govdi, Nadezda V. Sokolova, Irina V. Sorokina, Dmitry S. Baev, Tatyana G. Tolstikova, Victor I. Mamatyuk, Dmitry S. Fadeev, Sergey F. Vasilevsky, Valentine G. Nenajdenko , Med. Chem. Commun. , 2015 , 6 , 230