Abstract
The identification of metrics to assess sustainability of complex chemical synthesis routes has been a topic of interest in recent years. The diversity of life cycle assessment (LCA) approaches for fine chemicals and pharmaceuticals that have been developed face a common challenge: limited availability of production data. This critically affects completeness, accuracy, and reliability. Herein, we describe an iterative closed-loop approach, bridging life cycle assessment and multi-step synthesis development. Our comprehensive analysis leverages documented sustainability data augmented by infor-mation extrapolated from basic chemicals through retrosynthesis. The LCA results are discussed and evaluated against the more traditional process mass intensity (PMI). We have chosen the synthesis of the commercial antiviral drug Le-termovir as a case study: Implementation of LCA to the published route in parallel to a de novo synthesis enables us to benchmark, compare, and contrast routes. Identification of bottlenecks in both syntheses revealed negative impacts on the sustainability in asymmetric catalysis as well as metal-mediated couplings, highlighting the continued demand for sustainable catalysis that minimizes adverse effects on global warming potential, ecosystem quality, human health, and natural resources. This comprehensive strategy for multi-level sustainability assessment increases the accuracy, facili-tates comparisons, and enables targeted optimization of sustainability in organic chemistry.



![Author ORCID: We display the ORCID iD icon alongside authors names on our website to acknowledge that the ORCiD has been authenticated when entered by the user. To view the users ORCiD record click the icon. [opens in a new tab]](https://www.cambridge.org/engage/assets/public/coe/logo/orcid.png)