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Volumn 5, Issue 10, 2003, Pages 1789-1791

The C2 selective nucleophilic substitution reactions of 2,3-epoxy alcohols mediated by trialkyl borates: The first endo-mode epoxide-opening reaction through an intramolecular metal chelate

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; BORIC ACID; EPOXIDE; METAL CHELATE;

EID: 0141674890     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol034455f     Document Type: Article
Times cited : (94)

References (25)
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    • For C2 selective reactions with carbon nucleophiles. (a) Johnson, M. R.; Nakata, T.; Kishi, Y. Tetrahedron Lett. 1979, 20, 4343-4346. (b) Tius, M. A.; Fauq, A. H. J. Org. Chem. 1983, 48, 4131-4132. (c) Chong, J. M.; Cyr, D. R.; Mar, E. K. Tetrahedron Lett. 1987, 28, 5009-5012. (d) Lipshutz, B. H.; Sengupta, S. Org. React. 1992, 41, 135-631. (e) Sasaki, M.; Tanino, K.; Miyashita, M. Org. Lett. 2001, 3, 1765-1767.
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    • note
    • Calculations were performed with the GAUSSIAN 98 program at the B3LYP/6-31G*//HF/3-21G level. For details, see the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.