Enamine intermediates in the synthesis of analogs of pyrrolnitrin

DOI: 10.1002/jhet.5570110236

Source and publish data:

Journal of Heterocyclic Chemistry p. 275 - 277 (1974)

Update date:2022-08-05

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Authors:

Garcia Garcia

Benjamin

Fryer Fryer

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Article abstract of DOI:10.1002/jhet.5570110236

Full text of DOI:10.1002/jhet.5570110236

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Article Doi

Enamine intermediates in the synthesis of analogs of pyrrolnitrin

DOI: 10.1002/jhet.5570110236

Source and publish data:

Authors:

Article abstract of DOI:10.1002/jhet.5570110236

Full text of DOI:10.1002/jhet.5570110236

Products guided by the article

R&D Labs maybe for 52853-50-6

Relevant to this article

A NEW CARBON-CARBON BOND FORMING REACTION IN INDOLE CHEMISTRY. C3-ARYLATION AND ALKYLATION WITH PHENYL (β-INDOLYL)IODONIUM TRIFLUOROACETATE

Novel quinolinone-phosphonic acid AMPA antagonists devoid of nephrotoxicity.

Multifunctional thiosemicarbazones and deconstructed analogues as a strategy to study the involvement of metal chelation, Sigma-2 (σ2) receptor and P-gp protein in the cytotoxic action: In vitro and in vivo activity in pancreatic tumors

Letter: Synthesis of new beta-lactam antibiotics.

Addition Reaction of gem-Dichloroallyl Lithium to Benzophenones in the Presence of Macrocyclic Ligands: Formation of Chloro Oxiranes

A NEW CARBON-CARBON BOND FORMING REACTION IN INDOLE CHEMISTRY. C₃-ARYLATION AND ALKYLATION WITH PHENYL (β-INDOLYL)IODONIUM TRIFLUOROACETATE

Multifunctional thiosemicarbazones and deconstructed analogues as a strategy to study the involvement of metal chelation, Sigma-2 (σ₂) receptor and P-gp protein in the cytotoxic action: In vitro and in vivo activity in pancreatic tumors