317. A rearrangement of o-aminodiphenyl ethers. Part IV. N-alphylphenoxazines

Roberts, Kenneth C.; Clark, Hilda B.

doi:10.1039/jr9350001312

Cited by 13 publications

(4 citation statements)

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“…(377). 2-Mercapto-and 2-hydroxy-2', 4', 6'-trinitrodiphenylamines and related compounds are readily cyclized to, respectively, phenothiazines (599) and phenoxazines (equation 10) (486,489,562). The nitro groups displaced in these reactions are, it should be noted, situated meta to the activating nitro groups.…”

Section: Replacement Of the Nitro Groupmentioning

confidence: 99%

Aromatic Nucleophilic Substitution Reactions.

Bunnett¹,

Zahler²

1951

Chem. Rev.

1,046

500

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Section: Replacement Of the Nitro Groupmentioning

confidence: 99%

Aromatic Nucleophilic Substitution Reactions.

Bunnett¹,

Zahler²

1951

Chem. Rev.

1,046

500

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“…67 Most of these sequences were eventually released to GenBank without restrictions (and so also EMBL-EBI and the DDBJ). 68 The solution was about credit and not proprietary dealings with the data, and involved finding a balance between encouraging submissions while protecting confidentiality until the researchers doing the sequencing had an opportunity to gain credit (discussed further below).…”

Section: Submitters Are Advised That the Information Displayed On Thementioning

confidence: 99%

Open Access DNA, Rna and Amino Acid Sequences: The Consequences and Solutions for the International Regulation of Access and Benefit Sharing

Lawson

Rourke

2016

SSRN Journal

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This article addresses how open access to DNA, RNA and amino acid sequences might be reconciled with the benefit-sharing obligations under the United Nations' Convention on Biological Diversity and its Nagoya Protocol, the Food and Agriculture Organization of the United Nations' International Treaty on Plant Genetic Resources for Food and Agriculture, and the World Health Organization's Pandemic Influenza Preparedness Framework for the Sharing of Influenza Viruses and Access to Vaccines and Other Benefits. Tracing the evolution of open access databases, the article posits models for reconciling open access and benefit sharing; the article concludes, however, that none of the proposed solutions-monitoring and tracing, the contract model, and the copyright and database right model-provides a perfect solution. Each model does, however, suggest that open access to these sequences might be at least partially reconciled with benefit sharing.

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“…In the case of X = CH3, the rearrangement gave the phenoxazine (XXXII), which was evidently formed by cyclization of the expected rearrangement product. Synthetic N-methyl-o-hydroxydiphenylamine cyclized to give XXXII under the 0 XV \X\ N ch3 XXXII conditions of the rearrangement (229).…”

Section: N02mentioning

confidence: 99%

The Chemistry of the Diaryl Ethers.

Ungnade¹

1946

Chem. Rev.

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317. A rearrangement of o-aminodiphenyl ethers. Part IV. N-alphylphenoxazines

Cited by 13 publications

References 0 publications

Aromatic Nucleophilic Substitution Reactions.

Aromatic Nucleophilic Substitution Reactions.

Open Access DNA, Rna and Amino Acid Sequences: The Consequences and Solutions for the International Regulation of Access and Benefit Sharing

The Chemistry of the Diaryl Ethers.

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