Photocyclisation of enamides. Part 39. General strategy for the synthesis of pseudodistomins: synthesis of triacetates of (±)-tetrahydropseudodistomin and proposed structures of pseudodistomins A and B-Reference-Cited by-同舟云学术

Photocyclisation of enamides. Part 39. General strategy for the synthesis of pseudodistomins: synthesis of triacetates of (±)-tetrahydropseudodistomin and proposed structures of pseudodistomins A and B

Published:1996 Issue:3 Volume: Page:281-288
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Naito Takeaki,Yuumoto Yoko,Kiguchi Toshiko,Ninomiya Ichiya

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1996/P1/P19960000281

Reference21 articles.

1. Photocyclization of Enamides. 38. Reductive Photocyclization of a-(Methylthio)- and a-(Arylthio)enamides

2. First total synthesis of pseudodistomin tetrahydroacetate

3. Pseudodistomins A and B, novel antineoplastic piperdine alkaloids with calmodulin antagonistic activity from the Okinawan tunicate Pseudodistoma kanoko

4. Synthesis of (±)-Tetrahydropseudodistomin, a Hydrogenation Product of Antineoplastic Alkaloids, Pseudodistomins A and B

5. Synthesis of (+)-tetrahydropseudodistomin

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