메뉴 건너뛰기




Volumn 50, Issue 3, 2011, Pages 676-679

Formal syntheses of (-)- and (+)-phalarine

Author keywords

cross coupling; natural products; palladium; total synthesis

Indexed keywords

CROSS-COUPLINGS; FORMAL SYNTHESIS; HYPERVALENT IODINE; MODULAR APPROACH; NATURAL PRODUCTS; OXIDATIVE COUPLING REACTIONS; TITLE COMPOUNDS; TOTAL SYNTHESIS;

EID: 78651386231     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201006367     Document Type: Article
Times cited : (24)

References (23)
  • 4
    • 34247851027 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 1444-1447
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1444-1447
  • 6
    • 34247844617 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 1448-1450
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1448-1450
  • 11
    • 33750977591 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 7134-7186.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 7134-7186
  • 12
    • 36749031103 scopus 로고    scopus 로고
    • For related palladium-catalyzed vicinal aminoalkoxylation reactions of alkenes
    • K. Muñiz, J. Am. Chem. Soc. 2007, 129, 14542-14543. For related palladium-catalyzed vicinal aminoalkoxylation reactions of alkenes
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 14542-14543
    • Muñiz, K.1
  • 16
    • 34547480362 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 5737-5740
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 5737-5740
  • 19
    • 33846893890 scopus 로고    scopus 로고
    • For preparation of the stannane 7, see
    • L. Yin, J. Liebscher, Chem. Rev. 2007, 107, 133-173. For preparation of the stannane 7, see
    • (2007) Chem. Rev. , vol.107 , pp. 133-173
    • Yin, L.1    Liebscher, J.2
  • 22
    • 78651398166 scopus 로고    scopus 로고
    • A palladium-free oxidative aminoacetoxylation of alkene in the presence of hypervalent iodine reagent under acidic conditions was observed by Sorensen and co-workers, see Ref. [4b].
    • A palladium-free oxidative aminoacetoxylation of alkene in the presence of hypervalent iodine reagent under acidic conditions was observed by Sorensen and co-workers, see Ref. [4b].
  • 23
    • 78651381724 scopus 로고    scopus 로고
    • The acetonide 15 a and TBS ether 15 b were prepared from ketal 14 by a three-step procedure, involving deketalization, either acetonide formation (for 15 a) or TBS protection (for 15 b), and removal of the BOM ether. For details, see the Supporting Information.
    • The acetonide 15 a and TBS ether 15 b were prepared from ketal 14 by a three-step procedure, involving deketalization, either acetonide formation (for 15 a) or TBS protection (for 15 b), and removal of the BOM ether. For details, see the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.