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Volumn 30, Issue 5, 2009, Pages 1003-1008

Anti-Selective dihydroxylation reactions of monosubstituted and (E)-ester conjugated allylic amines by bulky alkyl groups

Author keywords

Amino alcohols; Asymmetric synthesis; Dihydroxylations; OBO ester

Indexed keywords

ALKYL GROUPS; ALLYLIC AMINES; AMINO ALCOHOLS; ANTI-SELECTIVITY; ASYMMETRIC SYNTHESIS; CHIRAL REAGENT; DIASTEREO-SELECTIVITY; DIHYDROXYLATION REACTION; DIHYDROXYLATIONS; EFFICIENT SYNTHESIS; ESTER GROUPS; GLUCOSIDASE; L-SERINE; OBO ESTER; STEREO-SELECTIVE; SYNTHETIC UTILITY;

EID: 70349859780     PISSN: 02532964     EISSN: 12295949     Source Type: Journal    
DOI: 10.5012/bkcs.2009.30.5.1003     Document Type: Article
Times cited : (7)

References (50)
  • 6
    • 11944249437 scopus 로고
    • For reviews see
    • For reviews, see: Cha, J. K.; Kim, N.-S. Chem. Rev. 1995, 95, 1761.
    • (1995) Chem. Rev. , vol.95 , pp. 1761
    • Cha, J.K.1    Kim, N.-S.2
  • 30
    • 70349867809 scopus 로고    scopus 로고
    • Note
    • 4,5 values of the trans γ-lactams with different side alkyl groups (Me, Bn, i-Bu and i-Pr) showed ca. 6.0 Hz, whereas the larger J4,5 values of 7.1-7.5 Hz were observed with the cis γ-lactams. Oh, J. S. Ph. D. Dissertation, Seoul National University, Seoul Republic of Korea, 2004.
  • 31
    • 70349880030 scopus 로고    scopus 로고
    • Note
    • The larger coupling constant of 7.3 Hz in oxazolidinones is generally attributed to the cis oxazolidinone structure (ref. 5(a) and references therein).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.