Literature DB >> 12489960

Stereospecific, enantiospecific total synthesis of the sarpagine indole alkaloids (E)16-epiaffinisine, (E)16-epinormacusine B, and dehydro-16-epiaffinisine.

Jianming Yu1, Xuebin Liao, James M Cook.   

Abstract

[reaction: see text] The first stereospecific total synthesis of the sarpagine indole alkaloids (E)16-epiaffinisine (1), (E)16-epinormacusine B (2), and dehydro-16-epiaffinisine (4) has been completed; this method has also resulted in the synthesis of dehydro-16-epinormacusine B (5). The formation of the required ether in both 4 and 5 was realized with complete control from the top face on treatment of the corresponding alcohols with DDQ/THF in 98% and 95% yields, respectively.

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Year:  2002        PMID: 12489960     DOI: 10.1021/ol020209c

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  5 in total

1.  Enantiospecific total synthesis of the important biogenetic intermediates along the ajmaline pathway, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epivellosimine and macusine A.

Authors:  Wenyuan Yin; M Shahjahan Kabir; Zhijian Wang; Sundari K Rallapalli; Jun Ma; James M Cook
Journal:  J Org Chem       Date:  2010-05-21       Impact factor: 4.354

2.  Access to the akuammiline family of alkaloids: total synthesis of (+)-scholarisine A.

Authors:  Gregory L Adams; Patrick J Carroll; Amos B Smith
Journal:  J Am Chem Soc       Date:  2012-12-26       Impact factor: 15.419

Review 3.  Sarpagine and Related Alkaloids.

Authors:  Ojas A Namjoshi; James M Cook
Journal:  Alkaloids Chem Biol       Date:  2015-10-09

4.  Synthesis of Structurally Diverse 2,3-Fused Indoles via Microwave-Assisted AgSbF6-Catalysed Intramolecular Difunctionalization of o-Alkynylanilines.

Authors:  Yuanqiong Huang; Yan Yang; Hongjian Song; Yuxiu Liu; Qingmin Wang
Journal:  Sci Rep       Date:  2015-08-27       Impact factor: 4.379

5.  Stereospecific total synthesis of the indole alkaloid ervincidine. Establishment of the C-6 hydroxyl stereochemistry.

Authors:  Sundari K Rallapalli; Ojas A Namjoshi; V V N Phani Babu Tiruveedhula; Jeffrey R Deschamps; James M Cook
Journal:  J Org Chem       Date:  2014-04-18       Impact factor: 4.354

  5 in total

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