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Volumn 133, Issue 51, 2011, Pages 20712-20715

Directing group-controlled hydrosilylation: Regioselective functionalization of alkyne

Author keywords

[No Author keywords available]

Indexed keywords

ACCELERATING EFFECT; HOMOPROPARGYLIC ALCOHOLS; REGIO-SELECTIVE; REGIOISOMERS; REGIOSELECTIVE FUNCTIONALIZATION; TRANSFORMATION REACTIONS;

EID: 84555195155     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja209553f     Document Type: Article
Times cited : (80)

References (42)
  • 18
    • 22244480386 scopus 로고    scopus 로고
    • Trost et al. reported an efficient approach for oxy-functionalized compounds from Z -silylalkenes by Ru-catalyzed hydrosilylation of alkynes
    • Trost et al. reported an efficient approach for oxy-functionalized compounds from Z -silylalkenes by Ru-catalyzed hydrosilylation of alkynes: Trost, B. M.; Ball, Z. T.; Laemmerhold, K. M. J. Am. Chem. Soc. 2005, 127, 10028
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 10028
    • Trost, B.M.1    Ball, Z.T.2    Laemmerhold, K.M.3
  • 28
    • 84555183293 scopus 로고
    • U.S. Patent 3419593
    • Willing, D. N. U.S. Patent 3419593, 1968.
    • (1968)
    • Willing, D.N.1
  • 29
    • 84555182094 scopus 로고
    • U.S. Patent 3775452
    • Karstedt, B. D. U.S. Patent 3775452, 1973.
    • (1973)
    • Karstedt, B.D.1
  • 33
    • 36749010679 scopus 로고    scopus 로고
    • Brookhart et al. reported Co-catalyzed intramolecular hydrogen transfer from an amine moiety to a DMVS group and proposed that DMVS acts as a DG
    • Brookhart et al. reported Co-catalyzed intramolecular hydrogen transfer from an amine moiety to a DMVS group and proposed that DMVS acts as a DG: Bolig, A. D.; Brookhart, M. J. Am. Chem. Soc. 2007, 129, 14544
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 14544
    • Bolig, A.D.1    Brookhart, M.2
  • 38
    • 33645801391 scopus 로고    scopus 로고
    • Tsipis and Kefalidis reported a pioneering theoretical study on alkyne hydrosilylation using a Pt(0) catalyst, where acetylene and phosphane were used as substrate and ligand, respectively
    • Tsipis and Kefalidis reported a pioneering theoretical study on alkyne hydrosilylation using a Pt(0) catalyst, where acetylene and phosphane were used as substrate and ligand, respectively: Tsipis, C. A.; Kefalidis, C. E. Organometallics 2006, 25, 1696
    • (2006) Organometallics , vol.25 , pp. 1696
    • Tsipis, C.A.1    Kefalidis, C.E.2
  • 39
    • 0001900153 scopus 로고
    • These results clearly indicate that hydrosilylation of TBS ether 7 is faster than that of alkyne 16. Regarding the substituent effect of the oxy-functional group at the propargylic position, Tsipis reported that hydrosilylation of propargylic alcohols is faster than that of non-substituted alkynes
    • These results clearly indicate that hydrosilylation of TBS ether 7 is faster than that of alkyne 16. Regarding the substituent effect of the oxy-functional group at the propargylic position, Tsipis reported that hydrosilylation of propargylic alcohols is faster than that of non-substituted alkynes: Tsipis, C. A. J. Organomet. Chem. 1980, 188, 53
    • (1980) J. Organomet. Chem. , vol.188 , pp. 53
    • Tsipis, C.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.