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January 1, 1992Journal of the Chemical Society Chemical Communications

Conjugated heterocumulenes. Synthesis of conjugated carbodiimides and their facile conversion via intramolecular cycloaddition into nitrogen heterocycles, quinoline and pyrido2,3-bindole (α-carboline) derivatives

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Authors

TSTakao SaitoKyoto Institute of TechnologyHOHiromasa OhmoriEFEiji FurunoTokyo University of Science

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Saito et al. (1992) studied this question.

synapsesocial.com/papers/6a9634eb78d14db02cfa080dhttps://doi.org/10.1039/c39920000022
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Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1On the Reaction of (Vinylimino)phosphoranes. Part 17. Preparation of N-Vinylcarbodiimides and Their [4+2] Cycloaddition with Several Dienophiles to Give Pyridine Ring System1991 · 17 citations
  2. 2Conjugated heterocumulenes. Synthesis of CC- and NC-conjugated ketenimines through a Wittig-type reaction and their conversion into hetero(carbo)cycles1989 · 22 citations
  3. 3Cycloaddition reactions of carbodiimides. The first example of an intramolecular Diels–Alder reaction of CC-conjugated carbodiimides1990 · 37 citations