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Published in 2021 at "Organic letters"
DOI: 10.1021/acs.orglett.1c02719
Abstract: An unusual exo-selective photoenolization/Diels-Alder reaction of electron-rich 2-methylbenzaldehydes and dienophiles containing a benzoyl group at its α position was reported herein. The chiral TADDOL-type ligand plays a key role in this process: (1) accelerating the…
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Keywords:
diels alder;
reaction;
exo selective;
photoenolization diels ... See more keywords
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Published in 2020 at "ACS Macro Letters"
DOI: 10.1021/acsmacrolett.0c00555
Abstract: Next-generation membranes use highly engineered polymeric structures with enhanced chain rigidity, yet difficulties in polymerization often limit molecular weights required for film formation. Addi...
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Keywords:
molecular weights;
reductive heck;
heck derived;
derived polynorbornenes ... See more keywords
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Published in 2018 at "ACS Sustainable Chemistry & Engineering"
DOI: 10.1021/acssuschemeng.8b02099
Abstract: An exo-selective catalytic Diels–Alder reaction was developed using a Lewis acid catalyst with size-exclusion structural design. Exploiting the steric effect, especially the steric attraction, the Lewis acid catalyst was able to reroute the reaction along…
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Keywords:
lewis acid;
diels alder;
acid catalyst;
reaction ... See more keywords
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Published in 2017 at "New Journal of Chemistry"
DOI: 10.1039/c7nj02168b
Abstract: An exo-selective one-pot synthesis of novel spiro[cyclohexanone-pyrandione] derivatives through two sequential organobase-catalysed 1,4-conjugate additions of pyran-2,4-dione precursors on diarylideneacetone derivatives is described. The resulting 7,11-diaryl-2-oxaspiro[5.5]undec-3-ene-1,5,9-triones were obtained as a 2 : 1 mixture of exo- and endo-diastereomers…
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Keywords:
spiro cyclohexanone;
cyclohexanone pyrandione;
exo selective;