Diazine-derived guanidines, isothioureas, and isoureas: Synthesis and attempts of configurational assignment
The utility of diazinyl substituted carbodiimides (1a‐c) for the synthesis of novel guanidines (2), isothioureas (3), and isoureas (4) is shown. Attempts to determine the stereochemistry of the target compounds using NOE difference spectroscopy or X‐ray analysis, respectively, are described.
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Published in: | Journal of heterocyclic chemistry Vol. 39; no. 4; pp. 695 - 702 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Hoboken
Wiley-Blackwell
01-07-2002
Wiley‐Blackwell |
Online Access: | Get full text |
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Summary: | The utility of diazinyl substituted carbodiimides (1a‐c) for the synthesis of novel guanidines (2), isothioureas (3), and isoureas (4) is shown. Attempts to determine the stereochemistry of the target compounds using NOE difference spectroscopy or X‐ray analysis, respectively, are described. |
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Bibliography: | ArticleID:JHET5570390414 ark:/67375/WNG-RPQL4LMB-N istex:6A7D8D8E2E260355BF6AF35E0DBC109C7C0F7D95 |
ISSN: | 0022-152X 1943-5193 |
DOI: | 10.1002/jhet.5570390414 |