Issue 12, 1991
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Photocyclisation of enamides. Part 35. New total syntheses of the ergot alkaloids (±)-chanoclavine-1 and (±)-isochanoclavine-I using a fragmentation of 3-amino alcohols

Ichiya Ninomiya,   Naoko Habe (née Kuninobu),   Toshiko Kiguchi  and  Takeaki Naito  

Abstract

A new synthetic route involving the fragmentation reaction of 3-amino alcohols for the total synthesis of 6,7-secoergoline alkaloids was developed and then successfully applied to the total syntheses of (±)-chanoclavine-I and (±)-isochanoclavine-I.

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Article information

DOI
https://doi.org/10.1039/P19910003275
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1991, 3275-3285

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Photocyclisation of enamides. Part 35. New total syntheses of the ergot alkaloids (±)-chanoclavine-1 and (±)-isochanoclavine-I using a fragmentation of 3-amino alcohols

I. Ninomiya, N. Habe (<em xmlns="http://www.rsc.org/schema/rscart38">née</em> Kuninobu), T. Kiguchi and T. Naito, J. Chem. Soc., Perkin Trans. 1, 1991, 3275 DOI: 10.1039/P19910003275

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