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Volumn 14, Issue 24, 2012, Pages 6306-6309

Complementary asymmetric routes to (R)-2-(7-hydroxy-2,3-dihydro-1 H-pyrrolo[1,2-a]indol-1-yl)acetate

Author keywords

[No Author keywords available]

Indexed keywords

(R) 2 (7 HYDROXY 2,3 DIHYDRO 1H PYRROLO(1,2 A)INDOL 1 YL)ACETATE; (R)-2-(7-HYDROXY-2,3-DIHYDRO-1H-PYRROLO(1,2-A)INDOL-1-YL)ACETATE; ACETIC ACID DERIVATIVE; DRUG DERIVATIVE; FINGOLIMOD; INDOLE DERIVATIVE; PROPANEDIOL DERIVATIVE; PYRROLE DERIVATIVE; SPHINGOSINE; SPHINGOSINE 1 PHOSPHATE RECEPTOR;

EID: 84871589941     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol303070k     Document Type: Article
Times cited : (31)

References (28)
  • 3
    • 84871546519 scopus 로고    scopus 로고
    • http://www.gilenya.com/info/multiple-sclerosis/multiple-sclerosis- information.jsp.
  • 20
    • 0002165370 scopus 로고
    • Another significant feature of N -acyl oxazolidinone 5 is that epimerization at the α-stereogenic carbon in these systems is strongly discouraged, suggesting that the R -stereochemistry at the asymmetric carbon atom would remain unaffected by the strongly basic conditions encountered during the dilithiation reaction. See: Evans, D. A. Aldrichimica Acta 1982, 15, 23-32
    • (1982) Aldrichimica Acta , vol.15 , pp. 23-32
    • Evans, D.A.1
  • 21
    • 0001597804 scopus 로고
    • Bis(ester) 11 was prepared in two steps from N -acyl oxazolidinone 5 by peroxolysis followed by methylation. For removal of the chiral auxiliary by lithium hydroxide/hydrogen peroxide, see: Evans, D. A.; Britton, T. C.; Ellman, J. A. Tetrahedron Lett. 1987, 28, 6141-6144
    • (1987) Tetrahedron Lett. , vol.28 , pp. 6141-6144
    • Evans, D.A.1    Britton, T.C.2    Ellman, J.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.