The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Asymmetric Synthesis of Hydrobenzofuranones via Desymmetrization of Cyclohexadienones Using the Intramolecular Stetter Reaction
Open accessAbstract
Dearomatization of phenols followed by oxidation affords cyclohexadienyloxyacetaldehydes, which produce hydrobenzofuranones via asymmetric intramolecular Stetter reaction in good to excellent yield. Quaternary as well as up to three contiguous stereocenters may be formed in good to excellent enantioselectivities and high diastereoselectivities.
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Citations
Cites
Nucleophilic Carbenes in Asymmetric Organocatalysis
Enders, D., & Balensiefer, T. (2004) · Accounts of Chemical Research · doi:10.1021/ar030050j · Cited by 1,045
A Highly Enantioselective Catalytic Intramolecular Stetter Reaction
Kerr, M. S., Read de Alaniz, J., & Rovis, T. (2002) · Journal of the American Chemical Society · doi:10.1021/ja027411v · Cited by 505
Self-citationHighly Stereoselective Radical Cyclization of Haloacetals Controlled by the Acetal Center
Villar, F., Kolly‐Kovac, T., Equey, O., & Renaud, P. (2003) · Chemistry - A European Journal · doi:10.1002/chem.200390180 · Cited by 55
Cited by
N‐heterocyclische Carbene als Organokatalysatoren
Marion, N., Díez‐González, S., & Nolan, S. P. (2007) · Angewandte Chemie · doi:10.1002/ange.200603380 · Cited by 428
Wadamoto, M., Phillips, E. M., Reynolds, T. E., & Scheidt, K. A. (2007) · Journal of the American Chemical Society · doi:10.1021/ja073987e · Cited by 255
Shee, S., Mukherjee, S., Gonnade, R. G., & Biju, A. T. (2020) · Organic Letters · doi:10.1021/acs.orglett.0c01756 · Cited by 34
Metadata
- Authors
- Liu, Q., & Rovis, T.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2006-02-02
- Volume
- 128
- Issue
- 8
- Pages
- 2552-2553
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W1994230458
- Cited by
- 296
- References
- 3
- FWCI
- 10.77
- Type
- journal article
- Language
- en
- Open access
- green
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