메뉴 건너뛰기




Volumn 133, Issue 7, 2011, Pages 2140-2143

A domino approach (hydrolysis/dehydrohalogenation/heck coupling) for the synthesis of styrene sulfonate salts

Author keywords

[No Author keywords available]

Indexed keywords

CATALYTIC SYSTEM; ENVIRONMENTALLY FRIENDLY SOLVENTS; IODOARENES; KEY FEATURE; PHOSPHINE-FREE; SHORT REACTION TIME; SYNTHETIC METHODOLOGY;

EID: 79951818689     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja111462h     Document Type: Article
Times cited : (22)

References (52)
  • 5
    • 79951818392 scopus 로고
    • Previous synthese of styrene sulfonate salts can be found at: U. S. Patent 5 231 223
    • Previous synthese of styrene sulfonate salts can be found at: Bader, A.; Arlt, D.; Fiedel, D.; Meier, S.; U. S. Patent 5 231 223, 1992;
    • (1992)
    • Bader, A.1    Arlt, D.2    Fiedel, D.3    Meier, S.4
  • 6
    • 79951821490 scopus 로고
    • Chem. Abstr. 1993, 118, 101659.
    • (1993) Chem. Abstr. , vol.118 , pp. 101659
  • 17
    • 79951822108 scopus 로고    scopus 로고
    • Chem. Abstr. 1997, 130, 4115.
    • (1997) Chem. Abstr. , vol.130 , pp. 4115
  • 19
    • 0004034472 scopus 로고
    • Chem. Abstr. 1993, 101659.
    • (1993) Chem. Abstr. , pp. 101659
  • 20
    • 79951844543 scopus 로고
    • Toyo Soda Mfg. Co., Ltd., Japan.: Application: JP, 136314 55064565
    • Toyo Soda Mfg. Co., Ltd., Japan.: Application: JP, 136314 55064565, 1978;
    • (1978)
  • 21
    • 79951843258 scopus 로고
    • Chem. Abstr. 1978, 93 204267.
    • (1978) Chem. Abstr. , vol.93 , pp. 204267
  • 23
    • 79951843883 scopus 로고
    • Chem. Abstr. 1974, 86, 43406.
    • (1974) Chem. Abstr. , vol.86 , pp. 43406
  • 40
    • 79951817775 scopus 로고    scopus 로고
    • note
    • Use of palladium(II) chloride instead of palladium(II) acetate gave nearly identical conversion in a test reaction; however, we chose palladium(II) acetate as a precatalyst for all further reactions.
  • 50
    • 79951836995 scopus 로고    scopus 로고
    • note
    • 3 to the same reaction mixture followed by heating under identical conditions gave 1 in 82% yield.
  • 52
    • 79951836372 scopus 로고    scopus 로고
    • note
    • 2, rt, 24 h), unfortunately, did not produce the corresponding hydrogenated product (28). This could be due to the catalytic amount (2 mol%) of Pd being used for the Heck coupling versus 0.5 equiv used for the hydrogenation based on ref 46.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.