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Beckmann Rearrangement – Master Organic Chemistry
Beckmann Rearrangement – Master Organic Chemistry

Mechanistic Insight into Self-Propagation of Organo-Mediated Beckmann  Rearrangement: A Combined Experimental and Computational Study | The  Journal of Organic Chemistry
Mechanistic Insight into Self-Propagation of Organo-Mediated Beckmann Rearrangement: A Combined Experimental and Computational Study | The Journal of Organic Chemistry

Synthesis of 6-alkyl analogues of the 1-azabicyclo[4.3.0]nonan-2-one system  by a strategy of geminal acylation and Beckmann rearrangement - Journal of  the Chemical Society, Perkin Transactions 1 (RSC Publishing)  DOI:10.1039/B108164K
Synthesis of 6-alkyl analogues of the 1-azabicyclo[4.3.0]nonan-2-one system by a strategy of geminal acylation and Beckmann rearrangement - Journal of the Chemical Society, Perkin Transactions 1 (RSC Publishing) DOI:10.1039/B108164K

Hydroxylamine-O-sulfonic acid - Wikipedia
Hydroxylamine-O-sulfonic acid - Wikipedia

The Mechanochemical Beckmann Rearrangement: An Eco-efficient  “Cut-and-Paste” Strategy to Design the “Good Old Amide Bond” | ACS  Sustainable Chemistry & Engineering
The Mechanochemical Beckmann Rearrangement: An Eco-efficient “Cut-and-Paste” Strategy to Design the “Good Old Amide Bond” | ACS Sustainable Chemistry & Engineering

Direct synthesis of secondary amides from ketones through Beckmann  rearrangement using O-(mesitylsulfonyl)hydroxylamine - ScienceDirect
Direct synthesis of secondary amides from ketones through Beckmann rearrangement using O-(mesitylsulfonyl)hydroxylamine - ScienceDirect

Table 3 from Mild, calcium catalysed Beckmann rearrangements. | Semantic  Scholar
Table 3 from Mild, calcium catalysed Beckmann rearrangements. | Semantic Scholar

The Mechanochemical Beckmann Rearrangement: An Eco-efficient  “Cut-and-Paste” Strategy to Design the “Good Old Amide Bond” | ACS  Sustainable Chemistry & Engineering
The Mechanochemical Beckmann Rearrangement: An Eco-efficient “Cut-and-Paste” Strategy to Design the “Good Old Amide Bond” | ACS Sustainable Chemistry & Engineering

Scope and Mechanism of a True Organocatalytic Beckmann Rearrangement with a  Boronic Acid/Perfluoropinacol System under Ambient Conditions | Journal of  the American Chemical Society
Scope and Mechanism of a True Organocatalytic Beckmann Rearrangement with a Boronic Acid/Perfluoropinacol System under Ambient Conditions | Journal of the American Chemical Society

Dichloroimidazolidinedione-Activated Beckmann Rearrangement of Ketoximes  for Accessing Amides and Lactams | The Journal of Organic Chemistry
Dichloroimidazolidinedione-Activated Beckmann Rearrangement of Ketoximes for Accessing Amides and Lactams | The Journal of Organic Chemistry

Beckmann Reaction - an overview | ScienceDirect Topics
Beckmann Reaction - an overview | ScienceDirect Topics

Hydroxylamine-mediated C–C amination via an aza-hock rearrangement | Nature  Communications
Hydroxylamine-mediated C–C amination via an aza-hock rearrangement | Nature Communications

Zinc(II)-Catalyzed Synthesis of Secondary Amides from Ketones via Beckmann  Rearrangement Using Hydroxylamine-O-sulfonic Acid in Aqueous Media
Zinc(II)-Catalyzed Synthesis of Secondary Amides from Ketones via Beckmann Rearrangement Using Hydroxylamine-O-sulfonic Acid in Aqueous Media

Dichloroimidazolidinedione-Activated Beckmann Rearrangement of Ketoximes  for Accessing Amides and Lactams | The Journal of Organic Chemistry
Dichloroimidazolidinedione-Activated Beckmann Rearrangement of Ketoximes for Accessing Amides and Lactams | The Journal of Organic Chemistry

Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic  Acid (HOSA). - Abstract - Europe PMC
Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC

Direct synthesis of secondary amides from ketones through Beckmann  rearrangement using O-(mesitylsulfonyl)hydroxylamine - ScienceDirect
Direct synthesis of secondary amides from ketones through Beckmann rearrangement using O-(mesitylsulfonyl)hydroxylamine - ScienceDirect

Synthesis and reactivity of heterocyclic hydroxylamine-O-sulfonates
Synthesis and reactivity of heterocyclic hydroxylamine-O-sulfonates

Beckmann Rearrangement of Ketoximes to Lactams by Triphosphazene Catalyst |  The Journal of Organic Chemistry
Beckmann Rearrangement of Ketoximes to Lactams by Triphosphazene Catalyst | The Journal of Organic Chemistry

Beckmann Reaction - an overview | ScienceDirect Topics
Beckmann Reaction - an overview | ScienceDirect Topics

Zinc(II)-Catalyzed Synthesis of Secondary Amides from Ketones via Beckmann  Rearrangement Using Hydroxylamine-O-sulfonic Acid in Aqueous  Media,Synthesis - X-MOL
Zinc(II)-Catalyzed Synthesis of Secondary Amides from Ketones via Beckmann Rearrangement Using Hydroxylamine-O-sulfonic Acid in Aqueous Media,Synthesis - X-MOL

Beckmann Rearrangement
Beckmann Rearrangement

PDF] Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using  Hydroxylamine-O-sulfonic Acid (HOSA) | Semantic Scholar
PDF] Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA) | Semantic Scholar

Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic  Acid (HOSA). - Abstract - Europe PMC
Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). - Abstract - Europe PMC

Hydroxylamine-mediated C–C amination via an aza-hock rearrangement | Nature  Communications
Hydroxylamine-mediated C–C amination via an aza-hock rearrangement | Nature Communications

Beckmann Rearrangement
Beckmann Rearrangement

Hydroxylamine-O-sulfonic acid - Wikipedia
Hydroxylamine-O-sulfonic acid - Wikipedia

Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic  Acid (HOSA)
Cu(OTf)2-Catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA)