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Volumn 8, Issue 1, 2013, Pages 80-83

Preparation of chiral α-substituted alaninates through an efficient diastereoselective synthesis of trisubstituted allylic alcohols

Author keywords

substituted alaninates; allylic compounds; amines; butane 1,2 diacetal protected L glyceraldehyde; diastereoselectivity

Indexed keywords

ALLYLIC ALCOHOL; ALLYLIC AMINES; ALLYLIC COMPOUNDS; BUTANE-1,2-DIACETAL-PROTECTED L -GLYCERALDEHYDE; DIASTEREO-SELECTIVITY; DIASTEREOSELECTIVE ADDITIONS; DIASTEREOSELECTIVE SYNTHESIS; QUATERNARY CARBON;

EID: 84871577866     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201200859     Document Type: Article
Times cited : (2)

References (51)
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  • 47
    • 0037120811 scopus 로고    scopus 로고
    • For a representative example of using an Overman rearrangement for the synthesis of a quaternary chiral allylic amine moiety of a complex natural product, see
    • Y. K. Chen, A. E. Lurain, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 12225-12231. For a representative example of using an Overman rearrangement for the synthesis of a quaternary chiral allylic amine moiety of a complex natural product, see
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 12225-12231
    • Chen, Y.K.1    Lurain, A.E.2    Walsh, P.J.3
  • 50
    • 33746922678 scopus 로고    scopus 로고
    • To convert the trichloroacetamide into the corresponding carbamates, a one-pot protocol was developed, see:, T. Nishikawa, D. Urabe, M. Tomita, T. Tsujimoto, T. Iwabuchi, M. Isobe, Org. Lett. 2006, 8, 3263. However, for the preparation of the Boc-protected allylic amine, a lower yield was observed in their study.
    • (2006) Org. Lett. , vol.8 , pp. 3263
    • Nishikawa, T.1    Urabe, D.2    Tomita, M.3    Tsujimoto, T.4    Iwabuchi, T.5    Isobe, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.