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- Deciphering chemical logic of fungal natural product biosynthesis through heterologous expression and genome mining. Chen-Yu Chiang, Masao Ohashi, Yi Tang
, Nat. Prod. Rep.
, 2023
, 40
, 89
- Lithium pipecolinate as a facile and efficient ligand for copper-catalyzed hydroxylation of aryl halides in water. Linhai Jing, Jiangtao Wei, Li Zhou, Zhiyong Huang, Zhengkai Li, Xiangge Zhou
, Chem. Commun.
, 2010
, 46
, 4767
- A photocatalytic traceless C–N bond formation/cleavage strategy enabling the use of (α-chiral) alkyl aldehydes as deoxygenative (chiral) alkyl radical equivalents. Hanyang Bao, Limeng Zheng, Qian Liu, Mingfeng Han, Ya Li, Miao Bao, Yuanqiang Li, Pucha Yan, Yunkui Liu
, Org. Chem. Front.
, 2023
, 10
, 5551
- Formation and hydrolysis of amide bonds by lipase A from Candida antarctica; exceptional features. Arto Liljeblad, Pauli Kallio, Marita Vainio, Jarmo Niemi, Liisa T. Kanerva
, Org. Biomol. Chem.
, 2010
, 8
, 886
- Biosynthetic medicinal chemistry of natural product drugs. Frank E. Koehn
, Med. Chem. Commun.
, 2012
, 3
, 854
- Dissecting non-ribosomal and polyketide biosynthetic machineries using electrospray ionization Fourier-Transform mass spectrometry. Pieter C. Dorrestein, Neil L. Kelleher
, Nat. Prod. Rep.
, 2006
, 23
, 893
- One-pot tandem enantioselective hydrogenation–hydroformylation synthesis of cyclic α-amino acids. Euneace Teoh, Eva M. Campi, W. Roy Jackson, Andrea J. Robinson
, New J. Chem.
, 2003
, 27
, 387
- Synthesis and evaluation of conformationally restricted inhibitors of aspartate semialdehyde dehydrogenase. Andrew S. Evitt, Russell J. Cox
, Mol. BioSyst.
, 2011
, 7
, 1564
- A non-immunosuppressive FK506 analogue with neuroregenerative activity produced from a genetically engineered Streptomyces strain. Pramod B. Shinde, Yeon Hee Ban, Jae-yeon Hwang, Yumi Cho, Yi-Ahn Chen, Eunji Cheong, Sang-Jip Nam, Ho Jeong Kwon, Yeo Joon Yoon
, RSC Adv.
, 2015
, 5
, 6823
- Synthesis and biological evaluation of rapamycin-derived, next generation small molecules. Shiva Krishna Reddy Guduru, Prabhat Arya
, Med. Chem. Commun.
, 2018
, 9
, 27