The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.
Mechanistic Manifold and New Developments of the Julia–Kocienski Reaction
Abstract
The Julia–Kocienski reaction has become indispensable in the synthetic organic chemist's olefination toolbox. Although the stereochemical outcome of the transformation is sometimes difficult to predict, some trends can be explained by an array of mechanistic hypotheses which have been put forward since the initial disclosure of the reaction. Moreover, several important developments have been recently reported and are summarised in this microreview. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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Cites
Molecular rearrangements of organosilicon compounds
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A Concise Formal Total Synthesis of TMC-95A/B Proteasome Inhibitors
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Stereocontrolled Total Synthesis of a Polyfunctional Carotenoid, Peridinin
Furuichi, N., Hara, H., Osaki, T., Nakano, M., Mori, H., & Katsumura, S. (2004) · The Journal of Organic Chemistry · doi:10.1021/jo048852v · Cited by 86
Total Synthesis of (−)‐Amphidinolide E
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3,5-Bis(trifluoromethyl)phenyl Sulfones in the Direct Julia−Kocienski Olefination
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An expedient approach to E,Z-dienes using the Julia olefination
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Highly Efficient Stereocontrolled Total Synthesis of the Polyfunctional Carotenoid Peridinin
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Cited by
Zhang, N., Samanta, S. R., Rosen, B. M., & Percec, V. (2014) · Chemical Reviews · doi:10.1021/cr400689s · Cited by 458
Functions, Therapeutic Applications, and Synthesis of Retinoids and Carotenoids
Álvarez, R., Vaz, B., Gronemeyer, H., & de Lera, Á. R. (2014) · Chemical Reviews · doi:10.1021/cr400126u · Cited by 260
Metadata
- Authors
- Aïssa, C.
- Venue
- European Journal of Organic Chemistry
- Publisher
- Wiley
- Published
- 2009-03-30
- Volume
- 2009
- Issue
- 12
- Pages
- 1831-1844
- ISSN
- 1099-0690 (ISSN-L)
- 1434-193X
- OpenAlex
- W2057033979
- Cited by
- 259
- References
- 15
- FWCI
- 10.54
- Type
- journal article
- Language
- en
- Open access
- closed
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