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Volumn 66, Issue 33, 2010, Pages 6340-6348

Synthesis of the Northern hemisphere of the briaranes

Author keywords

Allylation; Cyclolactonisation; Diels Alder; Oxidation; Sulfone

Indexed keywords

(2,6 DIMETHYL 4 TOSYLCYCLOHEX 2 ENYL)METHANOL; (2,6 DIMETHYL 4 TOSYLCYCLOHEX 3 ENYL)METHANOL; 1 (4 TOLYLSULFONYL) BUT 2 ENE; 1 METHYL 4 (PENTA 1,3 DIEN 2 YLSULFINYL) BENZENE; 2 (4 TOLYLSULFINYL) PENT 1 EN 3 OL; 2 (4 TOLYLSULFINYL) PENT 1 EN 3 YL METHANESULFONATE; 2 (4 TOLYLSULFONYL) PENT 3 EN 1 OL; 2 (4 TOLYLSULFONYL) PENTA 1,3 DIENE; 2 [6 [(TERT BUTYLDIMETHYLSILYLOXY)METHYL] 1,5 DIMETHYLCYCLOHEX 2 ENYL] N,N DIMETHYLACETAMIDE; 2 [6 [(TERT BUTYLDIMETHYLSILYLOXY)METHYL] 2 HYDROXY 1,5 DIMETHYL CYCLOHEX 3 ENYL] 2 HYDROXYETHYL 4 METHYLBENZENESULFONATE; 2 CYCLOHEXENONE; 4 [ (TERT BUTYLDIMETHYLSILYLOXY) METHYL] 3,5 DIMETHYLCYCLOHEX 2 ENONE; 4 [(TERT BUTYLDIMETHYLSILYLOXY)METHYL] 3 HYDROXY 3A,5 DIMETHYL 3,3A,4,5 TETRAHYDROBENZOFURAN 2 (7AH) ONE; 4 [(TERT BUTYLDIMETHYLSILYLOXY)METHYL] 3,5 DIMETHYLCYCLOHEX 2 ENOL; 4 [(TERT BUTYLDIMETHYLSILYLOXY)METHYL] 3A,5 DIMETHYL 4,5 DIHYDROBENZOFURAN 2,3 (3AH,7AH) DIONE; 4 [(TERT BUTYLDIMETHYLSILYLOXY)METHYL] 3A,5DIMETHYL 3,3A,4,5 TETRAHYDROBENZOFURAN 2 (7AH) ONE; 4 [(TERT BUTYLDIMETHYLSILYLOXY)METHYL] 7 IODO 3A,5 DIMETHYLHEXAHYDROBENZOFURAN 2 (3H) ONE; 5 [(TERT BUTYLDIMETHYLSILYLOXY)METHYL] 6 (1 HYDROXY 4 METHYLPENT 4 ENYL) 4,6 DIMETHYLCYCLOHEX 2 ENOL; BRIANTHEIN W; BUTENOLIDE; CYCLOHEXANE DERIVATIVE; LEWIS ACID; METHYL 2,6 DIMETHYL 4 (4 TOLYLSULFINYL) CYCLOHEX 3 ENECARBOXYLATE; METHYL 2,6 DIMETHYL 4 TOSYLCYCLOHEX 3 ENECARBOXYLATE; NATURAL PRODUCT; TERPENOID DERIVATIVE; TERT BUTYL [ (2,6 DIMETHYL 4 TOSYLCYCLOHEX 2 ENYL)METHOXY] DIMETHYLSILANE; TERT BUTYL [ (2,6 DIMETHYL 4 TOSYLCYCLOHEX 3 ENYL)METHOXY] DIMETHYLSILANE; UNCLASSIFIED DRUG;

EID: 77955778620     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.04.003     Document Type: Article
Times cited : (9)

References (43)
  • 12
    • 77955838282 scopus 로고    scopus 로고
    • note
    • 2: C, 64.38; H, 6.53. Found: C, 64.72; H, 6.54.
  • 23
    • 77955821606 scopus 로고    scopus 로고
    • note
    • 3Si requires 285.1886).
  • 32
    • 77955799011 scopus 로고    scopus 로고
    • note
    • Interestingly, a low yield of cyclohexenone 15 could be isolated from the reaction mixture.
  • 34
    • 77955838281 scopus 로고    scopus 로고
    • note
    • 3SiNa requires 335.2018).
  • 38
    • 77955802201 scopus 로고    scopus 로고
    • note
    • 2SiI requires 466.1638).
  • 39
    • 77955819215 scopus 로고    scopus 로고
    • note
    • 2Na requires 421.2206).
  • 41
    • 77955810719 scopus 로고    scopus 로고
    • note
    • 3Si requires 313.2199).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.