메뉴 건너뛰기




Volumn 50, Issue 51, 2011, Pages 12232-12235

Reversing the reactivity of carbonyl functions with phosphonium salts: Enantioselective total synthesis of (+)-centrolobine

Author keywords

alkylations; carbonyl reactivity; natural products; phosphonium salts; reductions

Indexed keywords

ALKYLATION REACTIONS; ASYMMETRIC TOTAL SYNTHESIS; CARBONYL FUNCTION; CARBONYL GROUPS; ENANTIOSELECTIVE TOTAL SYNTHESIS; NATURAL PRODUCTS; PHOSPHONIUM SALTS; TRIMETHYLSILYL;

EID: 83755184128     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201106046     Document Type: Article
Times cited : (41)

References (40)
  • 17
    • 84990134867 scopus 로고
    • 3. However, they studied only the methylation of a 1:1 mixture of aldehyde and ketone compounds, but not compounds that have an aldehyde and a ketone function in the same molecule. The substrates were rather simple and yields and selectivity were good to moderate
    • 3. However, they studied only the methylation of a 1:1 mixture of aldehyde and ketone compounds, but not compounds that have an aldehyde and a ketone function in the same molecule. The substrates were rather simple and yields and selectivity were good to moderate.
    • (1988) Angew. Chem. Int. Ed. Engl. , vol.27 , pp. 944
  • 18
    • 83755168147 scopus 로고    scopus 로고
    • The selective formation of the phosphonium salt was confirmed by an NMR study on substrate 1-d. See the Supporting Information for details
    • The selective formation of the phosphonium salt was confirmed by an NMR study on substrate 1-d. See the Supporting Information for details.
  • 40
    • 83755161711 scopus 로고    scopus 로고
    • After the transformation, the selectivity was determined by HPLC analysis on a chiral stationary phase. See the Supporting Information for details
    • After the transformation, the selectivity was determined by HPLC analysis on a chiral stationary phase. See the Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.