메뉴 건너뛰기




Volumn 12, Issue 19, 2010, Pages 4300-4303

Synthesis of inherently chiral azacalix[4]arenes and diazadioxacalix[4] arenes

Author keywords

[No Author keywords available]

Indexed keywords


EID: 77957145214     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol1017454     Document Type: Article
Times cited : (45)

References (49)
  • 2
    • 0004287470 scopus 로고    scopus 로고
    • Kluwer Academic Publishers: Dordrecht, Netherlands
    • Vystotsky, M.; Saadioui, M.; Böhmer, V. Calixarenes 2001; Kluwer Academic Publishers: Dordrecht, Netherlands, 2001; pp 250 - 265.
    • (2001) Calixarenes 2001 , pp. 250-265
    • Vystotsky, M.1    Saadioui, M.2    Böhmer, V.3
  • 19
    • 77953202146 scopus 로고    scopus 로고
    • See also 1d, e and references cited therein
    • Hu, S.-Z.; Chen, C.-F. Chem. Commun. 2010, 46, 4199-4201 See also 1d, e and references cited therein.
    • (2010) Chem. Commun. , vol.46 , pp. 4199-4201
    • Hu, S.-Z.1    Chen, C.-F.2
  • 45
    • 77957156354 scopus 로고    scopus 로고
    • The term "inherently chiral" is used to identify macrocycles that lack internal planes of symmetry due to asymmetrically disposed substituents. The inherently chiral heteracalix[4]arenes described in this letter undergo enantiomerization at ambient temperature. Future work will address post-cyclization derivativization to furnish resolvable enantiomers
    • The term "inherently chiral" is used to identify macrocycles that lack internal planes of symmetry due to asymmetrically disposed substituents. The inherently chiral heteracalix[4]arenes described in this letter undergo enantiomerization at ambient temperature. Future work will address post-cyclization derivativization to furnish resolvable enantiomers.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.