Enantioefficient Synthesis of α-Ergocryptine: First Direct Synthesis of (+)-Lysergic Acid-Reference-Cited by-同舟云学术

Enantioefficient Synthesis of α-Ergocryptine: First Direct Synthesis of (+)-Lysergic Acid

Published:2004-08-03 Issue:18 Volume:69 Page:5993-6000
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Moldvai István¹,Temesvári-Major Eszter¹,Incze Mária¹,Szentirmay Éva¹,Gács-Baitz Eszter¹,Szántay Csaba¹

Affiliation:

1. Chemical Research Center, Institute of Biomolecular Chemistry, Hungarian Academy of Sciences, POB 17, H-1525 Budapest, Hungary, and Research Group for Alkaloid Chemistry of the Hungarian Academy of Sciences, Budapest University of Technology and Economics, Gellért tér 4, H-1521 Budapest, Hungary

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo049209b

Reference36 articles.

1. The Merck Index, 12th ed.; Merck and Co. Inc. Whitehouse Station, New York, 1996; p 231.

2. (a) Somei, M.; Yokoyama, Y.; Murakami, Y.; Ninomiya, I.; Kiguchi, T.; Naito, T.Recent Synthetic Studies on theErgot Alkaloids and RelatedCompounds; The Alkaloids, Vol. 54; Cordell, G. A., Ed.; Academic Press: San Diego, CA, 2000; pp 191−257.

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