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Volumn 50, Issue 4, 1994, Pages 1073-1082

Conjugate addition of allylsilanes to α,β-unsaturated N-acyloxazolidinones

Author keywords

[No Author keywords available]

Indexed keywords

2 OXAZOLIDINONE DERIVATIVE;

EID: 0028137704     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)80818-8     Document Type: Article
Times cited : (39)

References (37)
  • 5
    • 0001311213 scopus 로고
    • Asymmetric 1,4-addition of organocuprates to chiral .alpha.,.beta.-unsaturated N-acyl-4-phenyl-2-oxazolidinones: a new approach to the synthesis of chiral .beta.-branched carboxylic acids
    • (1993) The Journal of Organic Chemistry , vol.58 , pp. 766
    • Nicolas1    Russell2    Hruby3
  • 13
  • 20
    • 85064355278 scopus 로고
    • Conjugate Addition of Allylsilanes with Subsequent Sila-Wagner-Meerwein Rearrangement: A Novel Methodology for Stereoselective Trimethylsilylcyclopentane Annulation
    • (1990) Synlett , pp. 429
    • Knolker1    Jones2    Pannek3
  • 29
    • 84913976251 scopus 로고    scopus 로고
    • The stereochemistry of 8a and 8b were not exactly determined. However, based on the proposed reaction mechanism in ref. 13, we presumed that the absolute configuration at C(β) of 8a is S and that of 8b is R.
  • 35
    • 84913976250 scopus 로고    scopus 로고
    • 2 (10 mL) at room temperature. The amount of molecular sieve required to obtained the highest stereoselectivity has been examined found that 0.1 g of 4A emolecular sieve to 1 mmol of substrate is the minimum quantity.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.