Chemical synthesis planning is a key aspect in many fields of chemistry, especially drug discovery. Recent implementations of machine learning and artificial intelligence techniques for retrosynthetic analysis have shown great potential to improve computational methods for synthesis planning. Herein, we present a multiscale, data-driven approach for retrosynthetic analysis with deep highway networks (DHN). We automatically extracted reaction rules (i.e., ways in which a molecule is produced) from a data set consisting of chemical reactions derived from U.S. patents. We performed the retrosynthetic reaction prediction task in two steps: first, we built a DHN model to predict which group of reactions (consisting of chemically similar reaction...
© 2019 The Royal Society of Chemistry. We present a supervised learning approach to predict the prod...
Identifying synthetic routes for molecules of interest is a crucial step when discovering new drugs ...
We investigated the effect of different training scenarios on predicting the (retro)synthesis of che...
Chemical synthesis planning is a key aspect in many fields of chemistry, especially drug discovery. ...
Retrosynthesis prediction is a fundamental problem in organic synthesis, where the task is to identi...
Synthetic organic chemists face a dearth of challenges in the efficient construction of functional m...
Copyright © 2020 American Chemical Society. This work presents efforts to augment the performance of...
Discovering new reactions, optimizing their performance, and extending the synthetically accessible ...
We present an extension of our Molecular Transformer model combined with a hyper-graph exploration s...
With the increasing application of deep-learning-based generative models for de novo molecule design...
Abstract Retrosynthesis is at the core of organic chemistry. Recently, the rapid gr...
State of the art computer-aided synthesis planning models are naturally biased toward commonly repor...
With the idea of retrosynthetic analysis, which was raised in the 1960s, chemical synthesis analysis...
The drug-like chemical space is estimated to be 10 to the power of 60 molecules, and the largest gen...
We demonstrate molecular similarity to be a surprisingly effective metric for proposing and ranking ...
© 2019 The Royal Society of Chemistry. We present a supervised learning approach to predict the prod...
Identifying synthetic routes for molecules of interest is a crucial step when discovering new drugs ...
We investigated the effect of different training scenarios on predicting the (retro)synthesis of che...
Chemical synthesis planning is a key aspect in many fields of chemistry, especially drug discovery. ...
Retrosynthesis prediction is a fundamental problem in organic synthesis, where the task is to identi...
Synthetic organic chemists face a dearth of challenges in the efficient construction of functional m...
Copyright © 2020 American Chemical Society. This work presents efforts to augment the performance of...
Discovering new reactions, optimizing their performance, and extending the synthetically accessible ...
We present an extension of our Molecular Transformer model combined with a hyper-graph exploration s...
With the increasing application of deep-learning-based generative models for de novo molecule design...
Abstract Retrosynthesis is at the core of organic chemistry. Recently, the rapid gr...
State of the art computer-aided synthesis planning models are naturally biased toward commonly repor...
With the idea of retrosynthetic analysis, which was raised in the 1960s, chemical synthesis analysis...
The drug-like chemical space is estimated to be 10 to the power of 60 molecules, and the largest gen...
We demonstrate molecular similarity to be a surprisingly effective metric for proposing and ranking ...
© 2019 The Royal Society of Chemistry. We present a supervised learning approach to predict the prod...
Identifying synthetic routes for molecules of interest is a crucial step when discovering new drugs ...
We investigated the effect of different training scenarios on predicting the (retro)synthesis of che...