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Volumn 55, Issue 22, 2016, Pages 6556-6560

Enantioselective total synthesis of (-)-terengganensine A

Author keywords

asymmetric synthesis; domino cyclization; hydroxylation; monoterpene indole alkaloids; total synthesis

Indexed keywords

ALKALOIDS; CHEMICAL COMPOUNDS; ENANTIOSELECTIVITY; HYDROGENATION; HYDROXYLATION; METABOLITES; MONOTERPENES; PLANTS (BOTANY); POLYCYCLIC AROMATIC HYDROCARBONS; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

EID: 84969630134     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201602374     Document Type: Article
Times cited : (58)

References (47)
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    • The presence of the spirocyclopentene unit in 6 might also be responsible for the observed high diastereoselectivity. Chlorination of C20-unsubstituted octahydroindolo[2,3-a]quinolizine under similar conditions afforded a mixture of two diastereomers. See:, L. J. Dolby, G. W. Gribble, J. Org. Chem. 1967, 32, 1391-1398.
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    • th ed., Butterworth-Heinemann, Elsevier, Burlington, . This compound can be stored for weeks in a freezer without noticeable degradation
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    • To our knowledge, there has been only one report dealing with the C3 benzoyloxylation of N-methyl indole by DBP under a radical mechanism (80 °C), see:, See also Ref. [16]
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.