메뉴 건너뛰기




Volumn 8, Issue 25, 2006, Pages 5729-5732

Asymmetric radical addition of ethers to enantiopure N-p-toluenesulfinyl aldimines, mediated by dimethylzinc-air

Author keywords

[No Author keywords available]

Indexed keywords

DIMETHYLZINC; DRUG DERIVATIVE; ETHER DERIVATIVE; FREE RADICAL; IMINE; ORGANOMETALLIC COMPOUND; SULFINIC ACID DERIVATIVE; SULFONAMIDE; TOLUENE; UNCLASSIFIED DRUG;

EID: 33846328726     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0621093     Document Type: Article
Times cited : (65)

References (61)
  • 11
    • 23044503907 scopus 로고    scopus 로고
    • Reviews on asymmetric radical addition to C=N bonds: (a) Friestad, G. K. Eur. J. Org. Chem. 2005, 3157-3172.
    • Reviews on asymmetric radical addition to C=N bonds: (a) Friestad, G. K. Eur. J. Org. Chem. 2005, 3157-3172.
  • 13
    • 33644652412 scopus 로고    scopus 로고
    • For selected recent examples on asymmetric radical addition to C= N bonds: (a) Miyabe, H.; Yamaoka, Y.; Takemoto, Y. J. Org. Chem. 2006, 71, 2099-2106.
    • For selected recent examples on asymmetric radical addition to C= N bonds: (a) Miyabe, H.; Yamaoka, Y.; Takemoto, Y. J. Org. Chem. 2006, 71, 2099-2106.
  • 20
    • 33747113614 scopus 로고    scopus 로고
    • For reviews on chemistry of N-sulfinyl imines: (a) Morton, D.; Stockman, R. A. Tetrahedron 2006, 62, 8869-8905.
    • For reviews on chemistry of N-sulfinyl imines: (a) Morton, D.; Stockman, R. A. Tetrahedron 2006, 62, 8869-8905.
  • 27
    • 33750316213 scopus 로고    scopus 로고
    • For latest examples of nucleophilic addition to chiral N-sulfinyl imines: (a) Sun, X.-W.; Xu, M.-H.; Lin, G.-Q. Org. Lett. 2006, 8, 4979-4982.
    • For latest examples of nucleophilic addition to chiral N-sulfinyl imines: (a) Sun, X.-W.; Xu, M.-H.; Lin, G.-Q. Org. Lett. 2006, 8, 4979-4982.
  • 55
    • 33846307529 scopus 로고    scopus 로고
    • The use of (R)-N-tert-butanesulfinyl benzaldehyde imine resulted in a complex mixture of products.
    • The use of (R)-N-tert-butanesulfinyl benzaldehyde imine resulted in a complex mixture of products.
  • 56
    • 33846291964 scopus 로고    scopus 로고
    • Adduct 11a was obtained in 73% yield with 73% ee when 60 equiv of dioxolane 10 was used.
    • Adduct 11a was obtained in 73% yield with 73% ee when 60 equiv of dioxolane 10 was used.
  • 57
    • 33846270458 scopus 로고    scopus 로고
    • Both Brönsted acid mediated and oxidative cleavage strategies led to either decomposition or recovery of starting material along with minimal product formation
    • Both Brönsted acid mediated and oxidative cleavage strategies led to either decomposition or recovery of starting material along with minimal product formation.
  • 58
    • 10644231048 scopus 로고    scopus 로고
    • N-Sulfinyl aldimines preferentially adopt a conformation in which the oxygen atom and imino group are synperiplanar: (a) Dobrowolski, J. Cz.; Kawȩcki, R. J. Mol. Struct. 2005, 734, 235-239.
    • N-Sulfinyl aldimines preferentially adopt a conformation in which the oxygen atom and imino group are synperiplanar: (a) Dobrowolski, J. Cz.; Kawȩcki, R. J. Mol. Struct. 2005, 734, 235-239.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.