Challenge: Text-to-molecule models have shown great potential across chemical applications . however, they rely on atom-level tokenizations, which limiting the ability of models to capture global structural context within molecules.
Approach: They propose a text-to-molecule model that uses substructure-level tokenizations to model global connectivity.
Outcome: The proposed model outperforms state-of-the-art models using only 2% of training tokens.

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Bridging the Gap Between Molecule and Textual Descriptions via Substructure-aware Alignment (2025.emnlp-main)

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Challenge: Existing models lack the ability to learn fine-grained alignments between molecules and their descriptions.
Approach: They propose a molecule–text learning framework based on substructure-aware alignments that augments original molecule-description pairs with additional alignment signals derived from molecular substructures and chemical phrases.
Outcome: The proposed framework outperforms state-of-the-art models on a wide range of molecular benchmarks.
BioT5+: Towards Generalized Biological Understanding with IUPAC Integration and Multi-task Tuning (2024.findings-acl)

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Challenge: BioT5+ is an extension of the BioT5, but lacked a nuanced understanding of molecular structures.
Approach: They propose a new bio-entity modeling framework, BioT5+, which integrates IUPAC names and molecule data.
Outcome: The proposed model bridges the gap between molecular representations and textual descriptions and improves the grounded reasoning of bio-text and bio-sequences.
Translation between Molecules and Natural Language (2022.emnlp-main)

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Challenge: MolT5 pretrains models on unlabeled natural language text and molecule strings . bringing a new drug to market can cost over a billion dollars and take over ten years .
Approach: They propose a self-supervised learning framework for pretraining models on unlabeled natural language text and molecule strings.
Outcome: The proposed framework pretrains models on unlabeled natural language text and molecule strings, and it generates high quality outputs.
BioT5: Enriching Cross-modal Integration in Biology with Chemical Knowledge and Natural Language Associations (2023.emnlp-main)

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Challenge: et al., 2022) argue that the current models for drug discovery lack the ability to integrate molecules, proteins, and natural language.
Approach: They propose a framework that integrates biological knowledge with chemical knowledge and natural language associations.
Outcome: The proposed framework shows superior performance across a wide range of tasks.
ByT5: Towards a Token-Free Future with Pre-trained Byte-to-Byte Models (2022.tacl-1)

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Challenge: a number of pre-trained language models use sequences of tokens corresponding to word units . token-free models that operate directly on raw text have many advantages .
Approach: They propose a standard Transformer architecture that can be used to process byte sequences . they also characterize trade-offs in terms of parameter count, training FLOPs, and inference speed .
Outcome: The proposed model is more robust to noise and more robust on spelling and pronunciation tasks.
Categorizing Semantic Representations for Neural Machine Translation (2022.coling-1)

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Challenge: Modern neural machine translation models suffer limitation in compositional generalization, resulting in weakened translation performance on unseen compounds.
Approach: They propose to introduce categorization to the contextualized representations to improve generalization by reducing sparsity and overfitting.
Outcome: The proposed method reduces compositional generalization error rates by 24% on a dedicated MT dataset.
ReactXT: Understanding Molecular “Reaction-ship” via Reaction-Contextualized Molecule-Text Pretraining (2024.findings-acl)

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Challenge: Molecular-text modeling is an emerging research field that aims to facilitate molecule-relevant tasks with a textual interface and textual knowledge.
Approach: They propose a new method for reaction-text modeling that uses three types of input contexts to incrementally pretrain LMs.
Outcome: The proposed method improves experimental procedure prediction and molecule captioning and offers competitive results in retrosynthesis.
CrystalICL: Enabling In-Context Learning for Crystal Generation (2025.emnlp-main)

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Challenge: Existing methods for crystal generation are limited to zero-shot scenarios and are unable to benefit from few-shot situations.
Approach: They propose a model designed for few-shot crystal generation that exploits in-context learning by capturing structure-property relationships from limited data.
Outcome: The proposed model reduces complexity of modeling crystal symmetry in LLMs and exploits ICL by capturing structure-property relationships from limited data.
Lost in Translation: Chemical Language Models and the Misunderstanding of Molecule Structures (2024.findings-emnlp)

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Challenge: chemistry and natural language processing (NLP) have advanced drug discovery.
Approach: They propose a framework for assessment of Chemistry LMs of different natures that relies on augmentations that preserve an underlying chemical.
Outcome: The proposed framework relies on augmentations that preserve an underlying chemical, such as kekulization and cycle replacements.
Learn Your Tokens: Word-Pooled Tokenization for Language Modeling (2023.findings-emnlp)

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Challenge: Language models typically tokenize text into subwords, using a deterministic, hand-engineered heuristic of combining characters into longer surface-level strings such as ‘ing’ or whole words.
Approach: They propose a 'learn your tokens' scheme which pooles bytes/characters into word representations and decodes individual characters/bytes per word in parallel.
Outcome: The proposed tokenizer outperforms subword models and byte/character models over the word boundary and outperformed on rare words by a factor of 30!

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