Journal article
Enhanced reactivity of tuned imidazolidin-2-one chiral auxiliaries in Diels–Alder reactions
Tetrahedron: Asymmetry, Vol.9(6), pp.923-926
1998
Abstract
Readily accessible alkyl 1-N-benzoyl-2-oxoimidazolidin-4-carboxylates display enhanced reactivity as efficient chiral auxiliaries in the Diels- Alder reaction of their 3-N-enoyl derivatives.
Details
- Title
- Enhanced reactivity of tuned imidazolidin-2-one chiral auxiliaries in Diels–Alder reactions
- Authors/Creators
- G.H.P. Roos (Author/Creator) - Sultan Qaboos UniversityS. Balasubramaniam (Author/Creator) - Murdoch University
- Publication Details
- Tetrahedron: Asymmetry, Vol.9(6), pp.923-926
- Publisher
- Elsevier Limited
- Identifiers
- 991005545518307891
- Murdoch Affiliation
- School of Mathematical and Physical Sciences
- Language
- English
- Resource Type
- Journal article
UN Sustainable Development Goals (SDGs)
This output has contributed to the advancement of the following goals:
Source: InCites
Metrics
19 Record Views
InCites Highlights
These are selected metrics from InCites Benchmarking & Analytics tool, related to this output
- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 2 Chemistry
- 2.1 Synthesis
- 2.1.945 Cyclopropanation Chemistry
- Web Of Science research areas
- Chemistry, Inorganic & Nuclear
- Chemistry, Organic
- Chemistry, Physical
- ESI research areas
- Chemistry