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rdf:type
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Description
| - Alpha-methylene lactones added stereoselectively various kinds of 1,3-dipolar compounds. Spiro pyrrolidines and spiro pyrrolizidines were prepared by addition of azomethin ylides generated from sarcosin and prolin resp. Cycloaddition of a photochemically generated nitril ylide showed an unusual exo-selectivity. Alpha-methylene-gamma-lactone with a bulky substituent (OBO) in gamma position, which was prepared as a single enantiomer from L-glutamic acid, added 1,3-dipolar compounds in anti-manner almost exclusively.
- Alpha-methylene lactones added stereoselectively various kinds of 1,3-dipolar compounds. Spiro pyrrolidines and spiro pyrrolizidines were prepared by addition of azomethin ylides generated from sarcosin and prolin resp. Cycloaddition of a photochemically generated nitril ylide showed an unusual exo-selectivity. Alpha-methylene-gamma-lactone with a bulky substituent (OBO) in gamma position, which was prepared as a single enantiomer from L-glutamic acid, added 1,3-dipolar compounds in anti-manner almost exclusively. (en)
- Alpha-methylene lactones added stereoselectively various kinds of 1,3-dipolar compounds. Spiro pyrrolidines and spiro pyrrolizidines were prepared by addition of azomethin ylides generated from sarcosin and prolin resp. Cycloaddition of a photochemically generated nitril ylide showed an unusual exo-selectivity. Alpha-methylene-gamma-lactone with a bulky substituent (OBO) in gamma position, which was prepared as a single enantiomer from L-glutamic acid, added 1,3-dipolar compounds in anti-manner almost exclusively. (cs)
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Title
| - Diastereoselectivity in 1,3-dipolar cycloaddition reactions of alpha-methylene lactone derivatives
- Diastereoselectivity in 1,3-dipolar cycloaddition reactions of alpha-methylene lactone derivatives (en)
- Diastereoselectivity in 1,3-dipolar cycloaddition reactions of alpha-methylene lactone derivatives (cs)
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skos:prefLabel
| - Diastereoselectivity in 1,3-dipolar cycloaddition reactions of alpha-methylene lactone derivatives
- Diastereoselectivity in 1,3-dipolar cycloaddition reactions of alpha-methylene lactone derivatives (en)
- Diastereoselectivity in 1,3-dipolar cycloaddition reactions of alpha-methylene lactone derivatives (cs)
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skos:notation
| - RIV/00216224:14310/01:00006003!RIV08-MSM-14310___
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http://linked.open.../vavai/riv/strany
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http://linked.open...avai/riv/aktivita
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http://linked.open...avai/riv/aktivity
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http://linked.open...vai/riv/dodaniDat
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http://linked.open...aciTvurceVysledku
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http://linked.open.../riv/druhVysledku
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http://linked.open...iv/duvernostUdaju
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http://linked.open...titaPredkladatele
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http://linked.open...dnocenehoVysledku
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http://linked.open...ai/riv/idVysledku
| - RIV/00216224:14310/01:00006003
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http://linked.open...riv/jazykVysledku
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http://linked.open.../riv/klicovaSlova
| - Stereoselectivity; Methylene Lactones; 1; 3-Dipolar Cycloaddition (en)
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http://linked.open.../riv/klicoveSlovo
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http://linked.open...ontrolniKodProRIV
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http://linked.open...v/mistoKonaniAkce
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http://linked.open...i/riv/mistoVydani
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http://linked.open...i/riv/nazevZdroje
| - 9th Meeting on Stereochemistry, Book of Abstracts
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http://linked.open...in/vavai/riv/obor
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http://linked.open...ichTvurcuVysledku
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http://linked.open...cetTvurcuVysledku
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http://linked.open...UplatneniVysledku
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http://linked.open...iv/tvurceVysledku
| - Mazal, Ctibor
- Melša, Petr
- Častulík, Jakub
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http://linked.open...vavai/riv/typAkce
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http://linked.open.../riv/zahajeniAkce
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http://linked.open...n/vavai/riv/zamer
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number of pages
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http://purl.org/ne...btex#hasPublisher
| - Vysoká škola chemicko-technologická v Praze; Česká společnost chemická
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https://schema.org/isbn
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http://localhost/t...ganizacniJednotka
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