A Cascade Cyclization of Orthogonally Protected Diaminodiazoketones to Sp<sup>3</sup>‐Enriched Fused 1,2,3‐Triazoles

Abstract A convenient approach to the synthesis of sp 3 ‐enriched bicyclic 1,2,3‐triazole derivatives based on the cascade cyclization of diaminodiazoketones with orthogonal protecting groups has been developed. The method is based on available commercial starting compounds and simple, environmentally acceptable synthesis methods. The formation of a condensed 1,2,3‐triazole ring is accompanied by the loss of chirality of the carbon atom near Boc‐amino group.

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Journal
ChemistrySelect
Published
2025-04-01
DOI
https://doi.org/10.1002/slct.202406027
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

A Cascade Cyclization of Orthogonally Protected Diaminodiazoketones to Sp3‐Enriched Fused 1,2,3‐Triazoles

Hanna Yakovleva, Dmitriy M. Volochnyuk, Serhii Bohza, Svitlana V. Shishkina et al.
ChemistrySelect
Click Chemistry and Applications
article

A Cascade Cyclization of Orthogonally Protected Diaminodiazoketones to Sp3‐Enriched Fused 1,2,3‐Triazoles

Hanna Yakovleva, Dmitriy M. Volochnyuk, Serhii Bohza, Svitlana V. Shishkina, Viacheslav Pendiukh, Oleg Svaljavin
article en

Abstract

Abstract A convenient approach to the synthesis of sp 3 ‐enriched bicyclic 1,2,3‐triazole derivatives based on the cascade cyclization of diaminodiazoketones with orthogonal protecting groups has been developed. The method is based on available commercial starting compounds and simple, environmentally acceptable synthesis methods. The formation of a condensed 1,2,3‐triazole ring is accompanied by the loss of chirality of the carbon atom near Boc‐amino group.

ChemistrySelectVol. 10(13)
State Scientific Institution “Institute for Single Crystals” of National Academy of Sciences of Ukraine (UA), Institute of Organic Chemistry (UA)
National Academy of Sciences of Ukraine
Openalex Percentile: Top 95%
Click Chemistry and Applications
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