메뉴 건너뛰기




Volumn 63, Issue 21, 1998, Pages 7180-7182

Facile and efficient synthesis of bolaamphiphilic tetraether phosphocholines

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000538452     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9803176     Document Type: Article
Times cited : (35)

References (29)
  • 20
    • 0040289315 scopus 로고
    • Vicens, J.; Böhmer, V., Eds.; Kluwer Academic: Dordrecht, Holland
    • The four hydroxy groups presumably trap water molecules, via hydrogen bonding, between lamellar plates formed by association of the polymethylene segments in a manner similar to that reported for calixarene solids. See: Atwood, J. L.; Bott, S. G. In Calixarenes: A Versatile Class of Macrocydic Compounds; Vicens, J.; Böhmer, V., Eds.; Kluwer Academic: Dordrecht, Holland, 1991; pp 199-210.
    • (1991) Calixarenes: A Versatile Class of Macrocydic Compounds , pp. 199-210
    • Atwood, J.L.1    Bott, S.G.2
  • 22
    • 0342788843 scopus 로고
    • Bittman and co-workers have also reported the synthesis of chiral benzyl glycidyl ethers from chiral glycidyl tosylates. See: Byun, H.-S.; Bittman, R. Tetrahedron Lett. 1989, 30, 2751-2754.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 2751-2754
    • Byun, H.-S.1    Bittman, R.2
  • 23
    • 85034158518 scopus 로고    scopus 로고
    • 2O-catalyzed addition of ω-chloroalkan-1-ols to rac-benzyl glycidyl ether. See: ref 11
    • 2O-catalyzed addition of ω-chloroalkan-1-ols to rac-benzyl glycidyl ether. See: ref 11.
  • 26
    • 85034156777 scopus 로고    scopus 로고
    • 11 required an additional three steps to effect the synthesis of closely related benzyl-protected tetraethers in lower net yields.
    • 11 required an additional three steps to effect the synthesis of closely related benzyl-protected tetraethers in lower net yields.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.