Victor B. Rybakov

Часть публикаций из профиля, по году от новых к старым. Это не полный список последних работ автора; работы без года — в конце.

• Concise and Free-Metal Access to Lactone-Annelated Pyrrolo[2,1-a]isoquinoline Derivatives via a 1,2-Rearrangement Step2024
• A Concise and Free‐Metal Access to Lactone Annelated Pyrrolo[2,1‐a]isoquinoline Derivatives via a 1,2‐Rearrangement Step2023
• CCDC 2091121: Experimental Crystal Structure Determination2023
• Donor–Acceptor Cyclopropane Ring Expansion to 1,2-Dihydronaphthalenes. Access to Bridged Seven-Membered Lactones2023
• Divergent and Nucleophile‐Assisted Rearrangement in the Construction of Pyrrolo[2,1‐b][3]benzazepine and Pyrido[2,1‐a]isoquinoline Scaffolds2023
• (3+3)‐Annulation of Donor–Acceptor Cyclopropanes with Diaziridines2018 · аннотациясвернуть

  The first example of (3+3)-annulation of two different three-membered rings is reported herein. Donor-acceptor cyclopropanes in reaction with diaziridines were found to afford perhydropyridazine derivatives in high…

• From Umpolung to Alternation: Modified Reactivity of Donor–Acceptor Cyclopropanes Towards Nucleophiles in Reaction with Nitroalkanes2016 · аннотациясвернуть

  A conceptually new type of donor-acceptor cyclopropane reactivity towards nucleophiles has been disclosed. An essential characteristic of the process is an unusual nucleophilic attack on the C(3)-position of a…

• Duality of Donor–Acceptor Cyclopropane Reactivity as a Three‐Carbon Component in Five‐Membered Ring Construction: [3+2] Annulation Versus [3+2] Cycloaddition2013 · аннотациясвернуть

  Quo vadis? The Lewis acid catalyzed reaction of (hetero)aryl-derived donor-acceptor cyclopropanes with alkenes can be selectively directed along a [3+2] annulation pathway (see scheme). This new process provides…