Two highly efficient syntheses of scalemic azocines

Tetrahedron Letters

Volumn 37, Issue 25, 1996, Pages 4317-4318

  Winkler, Jeffrey D ^a   Stelmach, John E ^a   Axten, Jeffrey ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; AZOCINE DERIVATIVE;

ALKYLATION; ARTICLE; CHEMICAL STRUCTURE; PHOTOCHEMISTRY; STEREOCHEMISTRY; SYNTHESIS; TRANS ISOMER; X RAY CRYSTALLOGRAPHY;

EID: 0030002630     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00834-9     Document Type: Article

References (19)

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2. a) Hino, T.; Nakagawa, M. J. Heterocyctic Chem. 1994, 31, 625;
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12. 3)=-85.04°.
13. 2, benzene, 75%
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16. The metathesis strategy for the synthesis of azocines has recently been reported independently by Martin (Martin, S.F.; Liao, Y.; Chen, H.; Patzel, M.; Ramser, M.N. Tetrahedron Lett. 1994, 35, 6005) and more recently by Pandit (Pandit, U.K. Farmaco 1995, 50, 749).
17. The metathesis strategy for the synthesis of azocines has recently been reported independently by Martin (Martin, S.F.; Liao, Y.; Chen, H.; Patzel, M.; Ramser, M.N. Tetrahedron Lett. 1994, 35, 6005) and more recently by Pandit (Pandit, U.K. Farmaco 1995, 50, 749).
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