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Volumn 47, Issue 5, 2008, Pages 840-871

More than bystanders: The effect of olefins on transition-metal-catalyzed cross-coupling reactions

Author keywords

Additives; Alkynes; Cross coupling homogeneous catalysis; Olefins

Indexed keywords

CATALYST ACTIVITY; LIGANDS; OLEFINS; REACTION KINETICS;

EID: 38549132389     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200700278     Document Type: Review
Times cited : (320)

References (219)
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    • These results are in contrast to those of Yamamoto et al, who obtained primarily ethane and ethene under similar reaction conditions. The reason for this discrepancy is not clear
    • These results are in contrast to those of Yamamoto et al., who obtained primarily ethane and ethene under similar reaction conditions. The reason for this discrepancy is not clear.
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    • this methodology was also utilized in the synthesis of chokol C: c B. M. Trost, L. T. Phan, Tetrahedron Lett. 1993, 34, 4735.
    • this methodology was also utilized in the synthesis of chokol C: c) B. M. Trost, L. T. Phan, Tetrahedron Lett. 1993, 34, 4735.
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    • It should be noted that a similar olefin effect is not observed with dialkyl palladium complexes containing PR3 ligands instead of bipy; see reference [34b] and a S. Komiya, Y. Akai, K. Tanaka, T. Yamamoto, A. Yamamoto, Organometallics 1985, 4, 1130;
    • 3 ligands instead of bipy; see reference [34b] and a) S. Komiya, Y. Akai, K. Tanaka, T. Yamamoto, A. Yamamoto, Organometallics 1985, 4, 1130;
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    • and references therein; For a review that includes metal-olefin species as active intermediates in catalytic cycles, see: a
    • For a review that includes metal-olefin species as active intermediates in catalytic cycles, see: a) G. Zasinnovich, G. Mestroni, S. Gladiali, Chem. Rev. 1992, 92, 1051, and references therein;
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    • It is well documented that metal coordination of a prochiral olefin on either face generates a chiral olefin for early work, see: G. Paiaro, A. Panunzi, J. Am. Chem. Soc. 1964, 86, 5148, This section deals with the use of dienes that display chirality prior to complexation or resolved complexes that are utilized in catalysis
    • It is well documented that metal coordination of a prochiral olefin on either face generates a chiral olefin (for early work, see: G. Paiaro, A. Panunzi, J. Am. Chem. Soc. 1964, 86, 5148). This section deals with the use of dienes that display chirality prior to complexation or resolved complexes that are utilized in catalysis.
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    • For examples of the use of asymmetric π-allyl fragments, see: a R. A. Fernandes, Y. Yamamoto, J. Org. Chem. 2004, 69, 3562;
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    • Hayashi and coworkers provide an example of such a reaction, see ref, 114j];
    • a) Hayashi and coworkers provide an example of such a reaction, see ref. [114j];
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    • We apologize for any potential oversight within this body of work. We invite the reader to contact one of the authors concerning any omission such that future updates of this area will be more comprehensive
    • We apologize for any potential oversight within this body of work. We invite the reader to contact one of the authors concerning any omission such that future updates of this area will be more comprehensive.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.