A stereoselective cyclization to carbafuranose derivatives starting from 1,4-bis-epoxides
- Author
- LMH Leung, AJ Boydell, V Gibson, ME Light and Bruno Linclau (UGent)
- Organization
- Abstract
- A concise synthesis of highly functionalized cyclopentane derivatives via a Brook rearrangement mediated stereoselective linchpin cyclization reaction involving tert-butyldimethylsilyl-1,3-dithianyllithium and homochiral 1,4-bis-epoxides is described.
- Keywords
- MULTICOMPONENT LINCHPIN COUPLINGS, METAL-HALOGEN EXCHANGE, CARBOCYCLIC, NUCLEOSIDES, BROOK REARRANGEMENT, IN-VITRO, ANALOGS, HIV, STRATEGIES, INHIBITOR, ARABITOL
Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-01GMMXB1RFKKRJ4M1F262E9BQV
- MLA
- Leung, LMH, et al. “A Stereoselective Cyclization to Carbafuranose Derivatives Starting from 1,4-Bis-Epoxides.” ORGANIC LETTERS, vol. 7, no. 23, 2005, pp. 5183–86, doi:10.1021/ol052009h.
- APA
- Leung, L., Boydell, A., Gibson, V., Light, M., & Linclau, B. (2005). A stereoselective cyclization to carbafuranose derivatives starting from 1,4-bis-epoxides. ORGANIC LETTERS, 7(23), 5183–5186. https://doi.org/10.1021/ol052009h
- Chicago author-date
- Leung, LMH, AJ Boydell, V Gibson, ME Light, and Bruno Linclau. 2005. “A Stereoselective Cyclization to Carbafuranose Derivatives Starting from 1,4-Bis-Epoxides.” ORGANIC LETTERS 7 (23): 5183–86. https://doi.org/10.1021/ol052009h.
- Chicago author-date (all authors)
- Leung, LMH, AJ Boydell, V Gibson, ME Light, and Bruno Linclau. 2005. “A Stereoselective Cyclization to Carbafuranose Derivatives Starting from 1,4-Bis-Epoxides.” ORGANIC LETTERS 7 (23): 5183–5186. doi:10.1021/ol052009h.
- Vancouver
- 1.Leung L, Boydell A, Gibson V, Light M, Linclau B. A stereoselective cyclization to carbafuranose derivatives starting from 1,4-bis-epoxides. ORGANIC LETTERS. 2005;7(23):5183–6.
- IEEE
- [1]L. Leung, A. Boydell, V. Gibson, M. Light, and B. Linclau, “A stereoselective cyclization to carbafuranose derivatives starting from 1,4-bis-epoxides,” ORGANIC LETTERS, vol. 7, no. 23, pp. 5183–5186, 2005.
@article{01GMMXB1RFKKRJ4M1F262E9BQV,
abstract = {{A concise synthesis of highly functionalized cyclopentane derivatives via a Brook rearrangement mediated stereoselective linchpin cyclization reaction involving tert-butyldimethylsilyl-1,3-dithianyllithium and homochiral 1,4-bis-epoxides is described.}},
author = {{Leung, LMH and Boydell, AJ and Gibson, V and Light, ME and Linclau, Bruno}},
issn = {{1523-7060}},
journal = {{ORGANIC LETTERS}},
keywords = {{MULTICOMPONENT LINCHPIN COUPLINGS,METAL-HALOGEN EXCHANGE,CARBOCYCLIC,NUCLEOSIDES,BROOK REARRANGEMENT,IN-VITRO,ANALOGS,HIV,STRATEGIES,INHIBITOR,ARABITOL}},
language = {{eng}},
number = {{23}},
pages = {{5183--5186}},
title = {{A stereoselective cyclization to carbafuranose derivatives starting from 1,4-bis-epoxides}},
url = {{http://doi.org/10.1021/ol052009h}},
volume = {{7}},
year = {{2005}},
}
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