Binghui Wang, Xu Ban and Zhiyong Jiang
Chem. Soc. Rev., 2026, Advance Article
Abstract
Bicyclo[1.1.0]butanes (BCBs), characterized by their compact and highly strained carbocyclic frameworks, have emerged as versatile building blocks in modern synthetic chemistry.
Xiang Liu, Jiawei He, Keyu Lin, Xingyue Wang and Hua Cao
Org. Chem. Front., 2024,11, 6942-6957
From themed collection:
FOCUS: Cycloaddition Chemistry
Abstract
This review primarily focuses on the latest developments in Lewis acid-catalyzed strain-release cycloaddition reactions of BCBs.
Shiksha Deswal, Rohan Chandra Das and Akkattu T. Biju
Chem. Soc. Rev., 2026, Advance Article
Abstract
This tutorial review provides an overview of the important structural features and reactivity modes of BCBs and delves deep into the recent advances in BCB chemistry for the synthesis of bicyclic scaffolds and functionalized cyclobutanes.
Eugenio RoĆ and Quentin Lefebvre
Org. Chem. Front., 2026,13, 2493-2598
From themed collection:
2026 Organic Chemistry Frontiers Review-type Articles
Abstract
This comprehensive review describes the methodologies reported between 2020 and early 2025 for the synthesis of (hetero)bicyclo[2.1.1]hexane derivatives, organised by mechanisms and the exit vectors achieved.
Xiang Zhou, Ye Hu, Yao Huang and Yang Xiong
Chem. Commun., 2025,61, 23-32
Abstract
Bicyclo[1.1.0]butanes have beautiful conformations, distinctive properties, and novel reactivities. We summarize and highlight the recent advances of its photochemical strain-release reactions relying on SET or EnT strategies.