Acid-mediated cyclizations of SEM-protected heterocyclic anilines and adjacent hydroxyls or enol-ethers - ScienceDirect
C-H bonds as ubiquitous functionality: a general approach to complex arylated imidazoles via regioselective sequential arylation of all three C-H bonds and regioselective N-alkylation enabled by SEM-group transposition. - Abstract - Europe
Organic Syntheses Procedure
Remarkable effect of 2,2′-bipyridyl : mild and highly chemoselective deprotection of methoxymethyl (MOM) ethers in combination with TMSOTf (TESOTf)–2, ... - Chemical Communications (RSC Publishing) DOI:10.1039/B907910F
C-H bonds as ubiquitous functionality: a general approach to complex arylated imidazoles via regioselective sequential arylation of all three C-H bonds and regioselective N-alkylation enabled by SEM-group transposition. - Abstract - Europe
Total Synthesis of Dibromoagelaspongin by Feldman
Synthesis of Raputimonoindoles A–C and Congeners - Kock - 2019 - European Journal of Organic Chemistry - Wiley Online Library
Scheme 7 Synthesis of neurodazine. Reagents and conditions: a) benzyl... | Download Scientific Diagram
Sonochemical protocol for protection and deprotection of functional groups in organic synthesis - ScienceDirect
Silyl Protective Groups | Chem-Station Int. Ed.
Protecting groups and deprotection- -OH, -COOH, C=O, -NH2 groups.
Molecules | Free Full-Text | An Efficient Synthesis of Aryl-Substituted Pyrroles by the Suzuki–Miyaura Coupling Reaction of SEM-Protected Pyrroles | HTML
Scheme 7 Synthesis of neurodazine. Reagents and conditions: a) benzyl... | Download Scientific Diagram
Acid-mediated cyclizations of SEM-protected heterocyclic anilines and adjacent hydroxyls or enol-ethers - ScienceDirect
Silyl Protective Groups | Chem-Station Int. Ed.
Organic Syntheses Procedure
Synthesis of Raputimonoindoles A–C and Congeners - Kock - 2019 - European Journal of Organic Chemistry - Wiley Online Library
Synthesis of Raputimonoindoles A–C and Congeners - Kock - 2019 - European Journal of Organic Chemistry - Wiley Online Library