Enantioselective Synthesis of Sealutomicin C-Reference-Cited by-同舟云学术

Enantioselective Synthesis of Sealutomicin C

Published:2024-06-17 Issue:26 Volume:146 Page:17757-17764
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Astle Stuart M.¹^ORCID,Guggiari Sean¹,Frost James R.²^ORCID,Hepburn Hamish B.³,Klauber David J.⁴^ORCID,Christensen Kirsten E.¹,Burton Jonathan W.¹^ORCID

Affiliation:

1. Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1 3TA, U.K.

2. UCB Pharma, 216 Bath Road, Slough, Berkshire SL1 3WE, U.K.

3. Vertex Pharmaceuticals, 86-88 Jubilee Avenue Milton Park, Abingdon OX14 4RW, U.K.

4. Chemical Development, Pharmaceutical Technology & Development, Operations, AstraZeneca, Macclesfield SK10 2NA, U.K.

Funder

AstraZeneca

Novartis

Engineering and Physical Sciences Research Council

UCB

Defence Science and Technology Laboratory

Diamond Light Source

Pfizer

GlaxoSmithKline

Vertex

Takeda

Evotec

Syngenta

Janssen

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.4c02969

Reference51 articles.

1. Sealutomicins, new enediyne antibiotics from the deep-sea actinomycete Nonomuraea sp. MM565M-173N2

2. Uncialamycin, A New Enediyne Antibiotic

3. Dynemicin A, a novel antibiotic with the anthraquinone and 1,5-diyn-3-ene subunit.

4. Strain Prioritization and Genome Mining for Enediyne Natural Products

5. Genome Mining of Micromonospora yangpuensis DSM 45577 as a Producer of an Anthraquinone-Fused Enediyne

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