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Volumn 74, Issue 8, 2009, Pages 2942-2946

Diastereoselectivity control of the radical carboazidation of substituted methylenecyclohexanes

Author keywords

[No Author keywords available]

Indexed keywords

BULKY SUBSTITUENTS; CARBOAZIDATION; CYCLOHEXYL; DETRIMENTAL EFFECTS; DIASTEREO SELECTIVITIES; EQUATORIAL ATTACKS; REACTION PATHWAYS; STEREOCONTROL; SUBSTITUTION PATTERNS; SYSTEMATIC STUDIES;

EID: 65249140699     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo900088x     Document Type: Article
Times cited : (32)

References (15)
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    • Ollivier, C.; Renaud, P. J. Am. Chem. Soc. 2000, 122, 6496-6497. Ollivier, C.; Renaud, P. J. Am. Chem. Soc. 2001, 123, 4717-4727.
  • 2
    • 0037119657 scopus 로고    scopus 로고
    • Renaud, P.; Ollivier, C.; Panchaud, P. Angew. Chem., Int. Ed. 2002, 41, 3460-3462. Panchaud, P.; Chabaud, L.; Landais, Y.; Ollivier, C.; Renaud, P.; Zigmantas, S. Chem.-Eur. J. 2004, 10, 3606-3614.
    • Renaud, P.; Ollivier, C.; Panchaud, P. Angew. Chem., Int. Ed. 2002, 41, 3460-3462. Panchaud, P.; Chabaud, L.; Landais, Y.; Ollivier, C.; Renaud, P.; Zigmantas, S. Chem.-Eur. J. 2004, 10, 3606-3614.
  • 5
    • 65249187103 scopus 로고    scopus 로고
    • Chabaud, L.; Landais, Y.; Renaud, P. Org. Lett. 2002, 4, 4257-4260. Chabaud, L.; Landais, Y.; Renaud, P.; Robert, F.; Castet, F.; Lucarini, M.; Schenk, K. Chem.-Eur. J. 2008, 14, 2744-2756. Masterson, D. S.; Porter, N. A. Org. Lett. 2002, 4, 4253-4256.
    • Chabaud, L.; Landais, Y.; Renaud, P. Org. Lett. 2002, 4, 4257-4260. Chabaud, L.; Landais, Y.; Renaud, P.; Robert, F.; Castet, F.; Lucarini, M.; Schenk, K. Chem.-Eur. J. 2008, 14, 2744-2756. Masterson, D. S.; Porter, N. A. Org. Lett. 2002, 4, 4253-4256.
  • 7
    • 33748784323 scopus 로고    scopus 로고
    • Falciola, C. A.; Tissot-Croset, K.; Alexakis, A. Angew. Chem., Int. Ed. 2006, 45, 5995-5998. Falciola, C. A.; Tissot-Croset, K.; Reyneri, H.; Alexakis, A. Adv. Synth. Catal. 2008, 350, 1090-1100.
    • Falciola, C. A.; Tissot-Croset, K.; Alexakis, A. Angew. Chem., Int. Ed. 2006, 45, 5995-5998. Falciola, C. A.; Tissot-Croset, K.; Reyneri, H.; Alexakis, A. Adv. Synth. Catal. 2008, 350, 1090-1100.
  • 8
    • 65249083811 scopus 로고    scopus 로고
    • Curran, D. P.; Porter, N. A.; Giese, B.Stereochemistry of radical reactions: concepts, guidelines, and synthetic applications; VCH: New York, 1996; p 280. Renaud, P. Stereoselectivity of Intermolecular Radical Reactions: Cyclic Systems. In Radicals in Organic Synthesis; Renaud, P.; Sibi, M. P., Eds.; Wiley-VCH: Weinheim, 2001; 1, pp 400-415.
    • Curran, D. P.; Porter, N. A.; Giese, B.Stereochemistry of radical reactions: concepts, guidelines, and synthetic applications; VCH: New York, 1996; p 280. Renaud, P. Stereoselectivity of Intermolecular Radical Reactions: Cyclic Systems. In Radicals in Organic Synthesis; Renaud, P.; Sibi, M. P., Eds.; Wiley-VCH: Weinheim, 2001; Vol. 1, pp 400-415.
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    • Wu, Y. D.; Houk, K. N. J. Am. Chem. Soc. 1987, 109, 908-910. Wu, Y. D.; Houk, K. N.; Trost, B. M. J. Am. Chem. Soc. 1987, 109, 5560-5561.
    • Wu, Y. D.; Houk, K. N. J. Am. Chem. Soc. 1987, 109, 908-910. Wu, Y. D.; Houk, K. N.; Trost, B. M. J. Am. Chem. Soc. 1987, 109, 5560-5561.
  • 15
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    • For simplicity reasons, the cis/trans nomenclature has been also used for 2,5-disubstitued cyclohexyl azides and takes into account only the relative configuration of the newly formed center and the substituent at position 2.
    • For simplicity reasons, the cis/trans nomenclature has been also used for 2,5-disubstitued cyclohexyl azides and takes into account only the relative configuration of the newly formed center and the substituent at position 2.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.