Formal Total Syntheses of (+)-Prelaureatin and (+)-Laurallene by Diastereoselective Brook Rearrangement-Mediated [3 + 4] Annulation-Reference-Cited by-同舟云学术

Formal Total Syntheses of (+)-Prelaureatin and (+)-Laurallene by Diastereoselective Brook Rearrangement-Mediated [3 + 4] Annulation

Published:2010-05-12 Issue:11 Volume:75 Page:3941-3943
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Sasaki Michiko¹,Oyamada Kazuhisa¹,Takeda Kei¹

Affiliation:

1. Department of Synthetic Organic Chemistry, Graduate School of Medical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-Ku, Hiroshima 734-8553, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo100708n

Reference39 articles.

1. Prelaureatin, a new biogenetic key intermediate isolated from Laurencia nipponica

2. Conversion of prelaureatin into laurallene, a bromo-allene compound, by enzymatic and chemical bromo-etherification reactions

3. Laurallene, new bromoallene from the marine red alga Yamada

4. Laureatin and isolaureatin, constituents of Laurencia nipponica Yamada

5. Isolaureatin, a constituent from yamada

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