TempRe: Template generation for single and direct multi-step retrosynthesis
Not on the map. Why?
Abstract (arXiv)
Retrosynthesis planning remains a central challenge in molecular discovery due to the vast and complex chemical reaction space. While traditional template-based methods offer tractability, they suffer from poor scalability and limited generalization, and template-free generative approaches risk generating invalid reactions. In this work, we propose TempRe, a generative framework that reformulates template-based approaches as sequence generation, enabling scalable, flexible, and chemically plausible retrosynthesis. We evaluated TempRe across single-step and multi-step retrosynthesis tasks, demonstrating its superiority over both template classification and SMILES-based generation methods. On the PaRoutes multi-step benchmark, TempRe achieves strong top-k route accuracy. Furthermore, we extend TempRe to direct multi-step synthesis route generation, providing a lightweight and efficient alternative to conventional single-step and search-based approaches. These results highlight the potential of template generative modeling as a powerful paradigm in computer-aided synthesis planning.
Key facts. Cited by 6 papers in the map (data through 14 Oct 2026). Builds on 14 of its 44 references that are in the map. First posted on arXiv 29 Jul 2025.
Builds on
14 of 44 references.
References · 14
- 2017Attention Is All You Needcited by 60,361
- 2014Adam: A Method for Stochastic Optimizationcited by 37,240
- 2017OpenNMT: Open-source Toolkit for Neural Machine Translationcited by 251
- 2018Molecular Transformer - A Model for Uncertainty-Calibrated Chemical Reaction Predictioncited by 229
- 2017Learning to Plan Chemical Synthesescited by 179
- 2017Retrosynthetic reaction prediction using neural sequence-to-sequence modelscited by 86
- 2020Retro*: Learning Retrosynthetic Planning with Neural Guided A* Searchcited by 76
- 2021Permutation invariant graph-to-sequence model for template-free retrosynthesis and reaction predictioncited by 68
- 2022Root-aligned SMILES: A Tight Representation for Chemical Reaction Predictioncited by 51
- 2023Re-evaluating Retrosynthesis Algorithms with Syntheseuscited by 27
- 2023Models Matter: The Impact of Single-Step Retrosynthesis on Synthesis Planningcited by 15
- 2021RetroComposer: Composing Templates for Template-Based Retrosynthesis Predictioncited by 13
Built on by
Citing papers per year: 2025: 1; 2026: 5.
6 papers.
- 2025SynthStrategy: Extracting and Formalizing Latent Strategic Insights from LLMs in Organic Chemistrycited by 3
- 2026Project Ariadne: Prompt-Conditioned Route Generation for Synthesis Planningcited by 1
- 2026Mechanistic Reaction Prediction via Discrete Flow Matching on Graph-Structured Electron Occupationcited by 1
- 2026RetroReasoner: A Reasoning LLM for Strategic Retrosynthesis Predictioncited by 0
- 2026Reinforced Reasoning for End-to-End Retrosynthetic Planningcited by 0
- 2026Strategy-first synthesis planning for complex natural productscited by 0
- 2026Mechanistic Reaction Prediction via Discrete Flow Matching on Graph-Structured Electron Occupation27 Aug 2026
- 2026Strategy-first synthesis planning for complex natural products7 Aug 2026
- 2026Project Ariadne: Prompt-Conditioned Route Generation for Synthesis Planning23 Jun 2026
- 2026Reinforced Reasoning for End-to-End Retrosynthetic Planning31 Mar 2026
- 2026RetroReasoner: A Reasoning LLM for Strategic Retrosynthesis Prediction13 Mar 2026
- 2025SynthStrategy: Extracting and Formalizing Latent Strategic Insights from LLMs in Organic Chemistry1 Dec 2025