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1
Published in 2020 at "Organic letters"
DOI: 10.1021/acs.orglett.0c02982
Abstract: Staudinger ligation is an attractive bio-orthogonal reaction that has been widely used to tag proteins, carbohydrates, and nucleic acids. Here, we explore the traceless variant of the Staudinger ligation for 3'-end modification of oligoribonucleotides. An…
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Keywords:
phosphine mediated;
bioconjugation end;
end;
rna ... See more keywords
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1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.1c04388
Abstract: A domino [2+4]/[2+3] sequential annulation reaction of MBH carbonates with N-unprotected indoles has been developed to provide various pyrroloquinoline derivatives in ≤94% yield and 20:1 dr. The reaction could be either mediated by stoichiometric PCy3…
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Keywords:
annulation construct;
sequential annulation;
mediated sequential;
annulation ... See more keywords
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0
Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b04248
Abstract: We herein report a phosphine-mediated domino process of MBH-type reaction/umpolung γ-addition through the rational integration of the privileged reactivities of alkynoate. Simply by manipulating the nucleophilic reagent, the developed protocol offers a facile, diversity-oriented construction…
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Keywords:
umpolung addition;
domino;
mbh type;
phosphine mediated ... See more keywords
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1
Published in 2022 at "Synlett"
DOI: 10.1055/s-0042-1751434
Abstract: A tertiary phosphine-mediated [3+2] cyclization reaction of ynones with fluorinated coumarin derivatives has been developed to give a series of coumarin-based CF3-containing furanones in moderate to good yields under mild reaction conditions. Preliminary investigation into…
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Keywords:
coumarin based;
phosphine mediated;
containing furanones;
mediated cyclization ... See more keywords