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Volumn 138, Issue 36, 2016, Pages 11970-11978

Stereoselective and Versatile Preparation of Tri- and Tetrasubstituted Allylic Amine Scaffolds under Mild Conditions

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; PALLADIUM; REACTION INTERMEDIATES; SCAFFOLDS; STEREOCHEMISTRY;

EID: 84987811240     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.6b07382     Document Type: Article
Times cited : (132)

References (97)
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    • Yi, C.S.1    Yun, S.Y.2
  • 37
    • 84856878519 scopus 로고    scopus 로고
    • Also see ref 4a. and 4b. Through allylic substitution reactions, see reference 3m
    • Lishchynskyi, A.; Muñiz, K. Chem.-Eur. J. 2012, 18, 2212-2216 Also see ref 4a. and 4b. Through allylic substitution reactions, see reference 3m 10.1002/chem.201103435
    • (2012) Chem. - Eur. J. , vol.18 , pp. 2212-2216
    • Lishchynskyi, A.1    Muñiz, K.2
  • 48
    • 0029091957 scopus 로고
    • By noncatalytic allylic substitutions
    • By noncatalytic allylic substitutions: Sen, S. E.; Roach, S. L. Synthesis 1995, 1995, 756-758 10.1055/s-1995-4012
    • (1995) Synthesis , vol.1995 , pp. 756-758
    • Sen, S.E.1    Roach, S.L.2
  • 62
    • 84906272238 scopus 로고    scopus 로고
    • The lower isolated yield is a consequence of a competitive side reaction that involves aminolysis of the cyclic carbonate by the amine reagent, which was indeed observed as a side product. Such aminolysis behavior has been well-documented; see, e.g., ref 10b, and the following: Blain, M.; Jean-Gérard, L.; Auvergne, R.; Benazet, D.; Caillol, S.; Andrioletti, B. Green Chem. 2014, 16, 4286-4291 10.1039/C4GC01032A
    • (2014) Green Chem. , vol.16 , pp. 4286-4291
    • Blain, M.1    Jean-Gérard, L.2    Auvergne, R.3    Benazet, D.4    Caillol, S.5    Andrioletti, B.6
  • 88
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    • Yuan, R.; Lin, Z. ACS Catal. 2015, 5, 2866-2872 10.1021/acscatal.5b00252
    • (2015) ACS Catal. , vol.5 , pp. 2866-2872
    • Yuan, R.1    Lin, Z.2
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    • Tsuji, J. Pure Appl. Chem. 1982, 54, 197-206 10.1351/pac198254010197
    • (1982) Pure Appl. Chem. , vol.54 , pp. 197-206
    • Tsuji, J.1
  • 96
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    • Similar observations regarding substituent effects on substrate reactivity were noted in related allylic chemistry: Trost, B. M.; Bunt, R. C.; Lemoine, R. C.; Calkins, T. L. J. Am. Chem. Soc. 2000, 122, 5968-5976 10.1021/ja000547d
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 5968-5976
    • Trost, B.M.1    Bunt, R.C.2    Lemoine, R.C.3    Calkins, T.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.