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Volumn 68, Issue 3, 2003, Pages 1146-1149

A mild deprotection strategy for allyl-protecting groups and its implications in sequence specific dendrimer synthesis

Author keywords

[No Author keywords available]

Indexed keywords

DEPROTECTION STRATEGY;

EID: 0037423340     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo026469p     Document Type: Article
Times cited : (87)

References (38)
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    • 3: (d) Dessolin, M.; Guillerez, M.G.; Thieriet, N.; Guibé, F.; Loffet, A. Tetrahedron Lett. 1995, 36, 5741. For palladium-catalyzed allyl cleavage under acidic conditions, see: (e) Smith, A. B., III; Rivero, R. A.; Hale, K. J.; Vaccaro, H. A. J. Am. Chem. Soc. 1991, 113, 2092. (f) Nakayama, K.; Uoto, K.; Higashi, K.; Soga, T.; Kusama, T. Chem. Pharm. Bull. 1992, 40, 1718. (g) In our methodology, we presume that carbonate anion acts as the nucleophile to react with the Pd-π-allyl species. However, note that this claim is unsubstantiated at this time.
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    • 3: (d) Dessolin, M.; Guillerez, M.G.; Thieriet, N.; Guibé, F.; Loffet, A. Tetrahedron Lett. 1995, 36, 5741. For palladium-catalyzed allyl cleavage under acidic conditions, see: (e) Smith, A. B., III; Rivero, R. A.; Hale, K. J.; Vaccaro, H. A. J. Am. Chem. Soc. 1991, 113, 2092. (f) Nakayama, K.; Uoto, K.; Higashi, K.; Soga, T.; Kusama, T. Chem. Pharm. Bull. 1992, 40, 1718. (g) In our methodology, we presume that carbonate anion acts as the nucleophile to react with the Pd-π-allyl species. However, note that this claim is unsubstantiated at this time.
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    • (1995) Tetrahedron Lett. , vol.36 , pp. 5741
    • Dessolin, M.1    Guillerez, M.G.2    Thieriet, N.3    Guibé, F.4    Loffet, A.5
  • 18
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    • 3: (d) Dessolin, M.; Guillerez, M.G.; Thieriet, N.; Guibé, F.; Loffet, A. Tetrahedron Lett. 1995, 36, 5741. For palladium-catalyzed allyl cleavage under acidic conditions, see: (e) Smith, A. B., III; Rivero, R. A.; Hale, K. J.; Vaccaro, H. A. J. Am. Chem. Soc. 1991, 113, 2092. (f) Nakayama, K.; Uoto, K.; Higashi, K.; Soga, T.; Kusama, T. Chem. Pharm. Bull. 1992, 40, 1718. (g) In our methodology, we presume that carbonate anion acts as the nucleophile to react with the Pd-π-allyl species. However, note that this claim is unsubstantiated at this time.
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  • 19
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    • (1992) Chem. Pharm. Bull. , vol.40 , pp. 1718
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    • note
    • 3: (d) Dessolin, M.; Guillerez, M.G.; Thieriet, N.; Guibé, F.; Loffet, A. Tetrahedron Lett. 1995, 36, 5741. For palladium-catalyzed allyl cleavage under acidic conditions, see: (e) Smith, A. B., III; Rivero, R. A.; Hale, K. J.; Vaccaro, H. A. J. Am. Chem. Soc. 1991, 113, 2092. (f) Nakayama, K.; Uoto, K.; Higashi, K.; Soga, T.; Kusama, T. Chem. Pharm. Bull. 1992, 40, 1718. (g) In our methodology, we presume that carbonate anion acts as the nucleophile to react with the Pd-π-allyl species. However, note that this claim is unsubstantiated at this time.
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    • Unpublished results from Tulane University
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    • note
    • When this reaction was carried out in ethanol, the corresponding deprotected ethyl ester was obtained as the only product. See also Table 1, entry 7.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.