메뉴 건너뛰기




Volumn 8, Issue 5, 2006, Pages 971-974

A formal [3,3]-sigmatropic rearrangement route to quaternary α-vinyl amino acids: Use of allylic N-PMP trifluoroacetimidates

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; FLUORINATED HYDROCARBON; IMIDOESTER; PALLADIUM;

EID: 33644943742     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol060019s     Document Type: Article
Times cited : (27)

References (49)
  • 28
    • 14544301554 scopus 로고    scopus 로고
    • For examples of thermal rearrangements (typically refluxing toluene for days) of allylic trichloroacetimidates to access quaternary centers in the lactacystin class of natural products, see: (a) Sato, H.; Maeba, T.; Yanase, R.; Yamaji-Hasegawa, A.; Kobayashi, T.; Chida, N. J. Antibiot. 2005, 58, 37-49.
    • (2005) J. Antibiot. , vol.58 , pp. 37-49
    • Sato, H.1    Maeba, T.2    Yanase, R.3    Yamaji-Hasegawa, A.4    Kobayashi, T.5    Chida, N.6
  • 38
    • 0041350419 scopus 로고    scopus 로고
    • Subsequently, Overman and co-workers reported asymmetric, Pd-(II) rearrangements of N-PMP trifluoroacetimidates in nonquaternary model systems: (a) Overman, L. E.; Owen, C. E.; Pavan, M. M.; Richards, C. J. Org. Lett. 2003, 5, 1809-1812.
    • (2003) Org. Lett. , vol.5 , pp. 1809-1812
    • Overman, L.E.1    Owen, C.E.2    Pavan, M.M.3    Richards, C.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.