Non-precious metals catalyze formal [4 + 2] cycloaddition reactions of 1,2-diazines and siloxyalkynes under ambient conditions.

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Non-precious metals catalyze formal [4 + 2] cycloaddition reactions of 1,2-diazines and siloxyalkynes under ambient conditions. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1021/OL501254H
P932PMC publication ID4076001
P698PubMed publication ID24911346
P5875ResearchGate publication ID262940416

P50authorYunus TürkmenQ57447193
P2093author name stringViresh H Rawal
Chintan S Sumaria
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Axially chiral biaryl diols catalyze highly enantioselective hetero-Diels-Alder reactions through hydrogen bondingQ81351509
Modified BINAP: the how and the whyQ81732507
Synthesis of 2-naphthols via carbonylative Stille coupling reaction of 2-bromobenzyl bromides with tributylallylstannane followed by the Heck reactionQ82457418
Chiral phosphoric acids: powerful organocatalysts for asymmetric addition reactions to iminesQ83835832
Synthesis of eight-membered lactones: intermolecular [6+2] cyclization of amphoteric molecules with siloxy alkynesQ84140520
One-pot synthesis of phthalazines and pyridazino-aromatics: a novel strategy for substituted naphthalenesQ84351679
Lewis acid catalyzed inverse electron-demand Diels-Alder reaction of 1,2-diazinesQ84759138
Enantioenriched synthesis of C1-symmetric BINOLs: iron-catalyzed cross-coupling of 2-naphthols and some mechanistic insightQ85011794
Tunable synthesis of 3-acyl-2-naphthols and 3-substituted isocoumarins via Jones reagent promoted cascade reactions of 2-(4-hydroxy-but-1-ynyl)benzaldehydesQ85744344
Domino inverse electron-demand Diels-Alder/cyclopropanation reaction of diazines catalyzed by a bidentate Lewis acidQ87445845
P433issue12
P407language of work or nameEnglishQ1860
P921main subjectcycloadditionQ898648
P304page(s)3236-3239
P577publication date2014-06-09
P1433published inOrganic LettersQ2396276
P1476titleNon-precious metals catalyze formal [4 + 2] cycloaddition reactions of 1,2-diazines and siloxyalkynes under ambient conditions
P478volume16

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cites work (P2860)
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