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Volumn 21, Issue 33, 2015, Pages 11855-11864

Asymmetric Total Synthesis of Indole Alkaloids Containing an Indoline Spiroaminal Framework

Author keywords

alkaloids; fused ring systems; natural products; spiro compounds; total synthesis

Indexed keywords

ALKALOIDS; CARBON; METABOLITES; NITROGEN COMPOUNDS; POLYCYCLIC AROMATIC HYDROCARBONS; STEREOSELECTIVITY;

EID: 84938422967     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201501150     Document Type: Article
Times cited : (22)

References (64)
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    • S. Omura, Tetrahedron 2011, 67, 6420-6459.
    • (2011) Tetrahedron , vol.67 , pp. 6420-6459
    • Omura, S.1
  • 33
    • 84938434204 scopus 로고    scopus 로고
    • Imidate 24 was treated with allyl tributylstannane instead of 22 to introduce an allyl group at C3a. Subsequently, removal of the Alloc group and protection of the resulting secondary amine with a Cbz group afforded the known intermediate of physovenine.[11a,14]
    • Imidate 24 was treated with allyl tributylstannane instead of 22 to introduce an allyl group at C3a. Subsequently, removal of the Alloc group and protection of the resulting secondary amine with a Cbz group afforded the known intermediate of physovenine.[11a,14]
  • 57
    • 0001668724 scopus 로고    scopus 로고
    • Angew. Chem. 2000, 112, 4768-4771.
    • (2000) Angew. Chem. , vol.112 , pp. 4768-4771


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.