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Volumn 5, Issue 8, 2014, Pages 3046-3056

Complete stereodivergence in the synthesis of 2-amino-1,3-diols from allenes

Author keywords

[No Author keywords available]

Indexed keywords

CHIRALITY; NITROGEN; STEREOCHEMISTRY;

EID: 84903715856     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c4sc01214c     Document Type: Article
Times cited : (25)

References (125)
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    • references therein For recent reviews on the synthesis of allenes, see
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    • Recent reviews on transformations utilizing allenes as starting materials or intermediates
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    • 10.1002/chir22256 For selected references on approaches to 1-amino-2,3-diol stereotriads, see
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  • 89
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    • 0003527522 scopus 로고
    • Conformational analysis of six-membered carbocyclic rings with exocyclic double bonds
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    • J. B. Lambert, Conformational analysis of six-membered carbocyclic rings with exocyclic double bonds, in The Conformational Analysis of Cyclohexenes, Cyclohexadienes, and Related Hydroaromatic Compounds, ed., P. W. Rabideau, VCH, New York, 1989, pp. 47-64
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    • Rearrangements and tautomerizations of enamines
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    • Z.-T. Huang and M.-X. Wang, Rearrangements and tautomerizations of enamines, in The Chemistry of Enamines, ed., Z. Rappoport, Wiley-Interscience, Chichester, 1994, vol. 2, pp. 889-922
    • (1994) The Chemistry of Enamines , vol.2
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    • Configuration, conformation and chiroptical properties of enamines
    • in, ed. Z. Rappoport, Wiley-Interscience, Chichester, 219-254 The 1,3-syn stereochemistry of the imines was inferred from the crystal structure of compound 43, as well as by comparison to the known 1,3-anti diastereomer
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    • See ESI for details. Interestingly, the stereochemical configuration of detoxinine was originally assigned with the arrangement shown in compound 68. For the study that revised the stereochemistry through synthesis of both stereoisomers, see
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.