Diastereoselective Syntheses of Indoloquinolizidines by a Pictet−Spengler/Lactamization Cascade-Reference-Cited by-同舟云学术

Diastereoselective Syntheses of Indoloquinolizidines by a Pictet−Spengler/Lactamization Cascade

Published:2010-11-09 Issue:23 Volume:12 Page:5366-5369
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Fang Huihui¹,Wu Xiaoyu¹,Nie Linlin¹,Dai Xiaoyang¹,Chen Jie¹,Cao Weiguo¹,Zhao Gang¹

Affiliation:

1. Department of Chemistry, Shanghai University, 99 Shangda Road, Shanghai 200444, China, and Key Laboratory of Synthetic Organic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol101922h

Reference62 articles.

1. bSzántay, C. and Honty, K.InThe Chemistry of Heterocyclic Compounds;Saxton, J. E., Ed.Wiley:New York, 1994; Vol. 25, pp161−216.

2. cBaxter, E. W. and Mariano, P. S.InAlkaloids: Chemical and Biological Perspectives;Pelletier, S. W., Ed.Springer:New York, 1992; Vol 8, pp197−319.

3. For selected examples of quinolizidine syntheses based on starting materials from the chiral pool, see:

4. An Enantioselective Total Synthesis of (+)-Geissoschizine

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