About: Enantioselective Organocatalytic Synthesis of 5 and 6 Membered Heterocycles     Goto   Sponge   NotDistinct   Permalink

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Description
  • During last decade the field of Organocatalysis emerged as one of the cornerstones of organic asymmetric synthesis. The use of organocatalysis has some advantages such as metal free reactions, environmentally friendly conditions, does not need to use dry solvents or inert atmosphere, avoid the use of protecting groups, etc... For these reasons, several research groups have focused their efforts on the development of new organocatalytic methodologies that render the final products in excellent yields and stereoselectivities. Concretely, the organocatalytic synthesis of 5 and 6 membered heterocycles has attracted much attention. In this review we have the aim to describe the different organocatalytic methodologies developed since in the synthesis of 5 and 6 heterocycles.
  • During last decade the field of Organocatalysis emerged as one of the cornerstones of organic asymmetric synthesis. The use of organocatalysis has some advantages such as metal free reactions, environmentally friendly conditions, does not need to use dry solvents or inert atmosphere, avoid the use of protecting groups, etc... For these reasons, several research groups have focused their efforts on the development of new organocatalytic methodologies that render the final products in excellent yields and stereoselectivities. Concretely, the organocatalytic synthesis of 5 and 6 membered heterocycles has attracted much attention. In this review we have the aim to describe the different organocatalytic methodologies developed since in the synthesis of 5 and 6 heterocycles. (en)
Title
  • Enantioselective Organocatalytic Synthesis of 5 and 6 Membered Heterocycles
  • Enantioselective Organocatalytic Synthesis of 5 and 6 Membered Heterocycles (en)
skos:prefLabel
  • Enantioselective Organocatalytic Synthesis of 5 and 6 Membered Heterocycles
  • Enantioselective Organocatalytic Synthesis of 5 and 6 Membered Heterocycles (en)
skos:notation
  • RIV/00216208:11310/11:10105200!RIV12-MSM-11310___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • Z(MSM0021620857)
http://linked.open...iv/cisloPeriodika
  • 24
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 197432
http://linked.open...ai/riv/idVysledku
  • RIV/00216208:11310/11:10105200
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • cascade reaction; azomethine ylides; conjugate addition; alpha,beta-unsaturated aldehydes; nitroso aldol/michael reaction; asymmetric 1,3-dipolar cycloaddition; michael-aldol reactions; pictet-spengler reactions; one-pot synthesis; Diels-Alder reaction (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • NL - Nizozemsko
http://linked.open...ontrolniKodProRIV
  • [2F43BC25513E]
http://linked.open...i/riv/nazevZdroje
  • Current Organic Chemistry
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 15
http://linked.open...iv/tvurceVysledku
  • Veselý, Jan
  • Rios, Ramon
http://linked.open...ain/vavai/riv/wos
  • 000299645800003
http://linked.open...n/vavai/riv/zamer
issn
  • 1385-2728
number of pages
http://localhost/t...ganizacniJednotka
  • 11310
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