Photocyclization of n-chloroacetyl derivatives of indolylethylamines to azepinoindoles and azocinoindoles. Correlation of the reactivity of indole radicals with frontier electron densities calculated by unrestricted hartree-fock mo-Reference-Cited by-同舟云学术

Photocyclization of n-chloroacetyl derivatives of indolylethylamines to azepinoindoles and azocinoindoles. Correlation of the reactivity of indole radicals with frontier electron densities calculated by unrestricted hartree-fock mo

Published:1975-01 Issue:39 Volume:16 Page:3399-3402
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Naruto Shunji,Yonemitsu Osamu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference20 articles.

1. Photoreductions and Photocyclizations of Tryptophan

2. Photocyclizations of N-chloroacetyltyramine. I. Formation of novel dimeric cage compounds

3. Photocyclizations of N-chloroacetyltyramines. II. Flash photolysis and substituent effect studies on the formation of dimeric cage compounds, and novel acid-catalyzed reversion

4. Mechanisms of photochemical reactions in solution. LXV. Quenching of excited singlet states of electron-rich aromatic compounds by methyl chloroacetate

5. EXCIPLEXES AND CAGE COMPLEXES IN THE PHOTOLYSIS OF N-CHLOROACETYLMESCALINE AND OTHER PHENETHYLAMINES

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