Efficient Syntheses of Korupensamines A, B and Michellamine B by Asymmetric Suzuki-Miyaura Coupling Reactions-Reference-Cited by-同舟云学术

Efficient Syntheses of Korupensamines A, B and Michellamine B by Asymmetric Suzuki-Miyaura Coupling Reactions

Published:2013-10-28 Issue:2 Volume:136 Page:570-573
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Xu Guangqing¹,Fu Wenzhen¹,Liu Guodu¹,Senanayake Chris H.²,Tang Wenjun¹

Affiliation:

1. State Key Laboratory of Bio-Organic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China

2. Chemical Development, Boehringer Ingelheim Pharmaceuticals Inc, Ridgefield, Connecticut CT06877, United States

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja409669r

Reference63 articles.

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2. Anti-HIV Michellamines from Ancistrocladus korupensis

3. Michellamines D−F, New HIV-Inhibitory Dimeric Naphthylisoquinoline Alkaloids, and Korupensamine E, a New Antimalarial Monomer, from Ancistrocladus korupensis

4. dBringmann, G.; Pokorny, F.InThe Alkaloids;Cordell, G. A., Ed.Academic Press:New York, 1995; Vol.46, pp127.

5. Korupensamines A-D, Novel Antimalarial Alkaloids from Ancistrocladus korupensis

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