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Volumn 19, Issue 9, 2008, Pages 1134-1138

Corrigendum to "Stereoselective total synthesis of (+)-pinellic acid from l-(+)-tartaric acid". [Tetrahedron: Asymmetry 19 (2008) 1134] (DOI:10.1016/j.tetasy.2008.04.015);Stereoselective total synthesis of (+)-pinellic acid from l-(+)-tartaric acid

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; GAMMA HYDROXYBUTYRAMIDE; NATURAL PRODUCT; PINELLIC ACID; TARTARIC ACID;

EID: 43649090982     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2008.05.026     Document Type: Erratum
Times cited : (24)

References (18)
  • 5
    • 33846245038 scopus 로고    scopus 로고
    • For an optimized synthesis of γ-oxo-amides by controlled addition of Grignard reagents to 4 , see: K.R. Prasad A. Chamdrakumar Tetrahedron 63 2007 1798
    • (2007) Tetrahedron , vol.63 , pp. 1798
    • Prasad, K.R.1    Chamdrakumar, A.2
  • 6
    • 31444450052 scopus 로고    scopus 로고
    • (a) Application of γ-hydroxybutyramides in the synthesis of natural products see: K.R. Prasad P. Anbarasan Tetrahedron Lett. 47 2006 1433
    • (2006) Tetrahedron Lett. , vol.47 , pp. 1433
    • Prasad, K.R.1    Anbarasan, P.2
  • 16
    • 0000377359 scopus 로고
    • 4, K-selectride produced alcohols with varied selectivity. The alcohols were inseparable at this stage. The formation of the major diastereomer can be attributed to the addition of hydride either by a Cram/Felkin open chain model or by a β-chelation, similar to that reported by Chikasita et al.: H. Chikashita T. Nikaya H. Uemura K. Itoh Bull. Chem. Soc. Jpn. 62 1989 2121
    • (1989) Bull. Chem. Soc. Jpn. , vol.62 , pp. 2121
    • Chikashita, H.1    Nikaya, T.2    Uemura, H.3    Itoh, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.