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- Asymmetric [3+2]-cyclization of α-imino amide surrogates to construct 3,4-diaminopyrrolidine-2,5-diones. Peiran Ruan, Cefei Zhang, Jin Wu, Fengnan Xiao, Yongyan Zhang, Qingfa Tan, Zhishan Su, Xiaoming Feng, Xiaohua Liu
, Chem. Commun.
, 2023
, 59
, 8250
- The chemistry and biology of organic guanidine derivatives. Roberto G. S. Berlinck, Antonio Carlos B. Burtoloso, Miriam H. Kossuga
, Nat. Prod. Rep.
, 2008
, 25
, 919
- Catalytic asymmetric formal [3+2] cycloaddition of isatogens with azlactones to construct indolin-3-one derivatives. Lihua Xie, Yi Li, Shunxi Dong, Xiaoming Feng, Xiaohua Liu
, Chem. Commun.
, 2021
, 57
, 239
- New synthetic routes to α-amino acids and γ-oxygenated α-amino acids. Reductive denitration and oxidative transformations of γ-nitro-α-amino acids. Maxwell J. Crossley, Yik M. Fung, Efstathia Kyriakopoulos, Jeffrey J. Potter
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 1123
- Conjugate additions of organocuprates to a 3-methylene-6-isopropyldiketopiperazine acceptor for the asymmetric synthesis of homochiral α-amino acids. Steven D. Bull, Stephen G. Davies, A. Christopher Garner, Michael D. O'Shea
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 3281
- Type II non-ribosomal peptide synthetase proteins: structure, mechanism, and protein–protein interactions. Matt J. Jaremko, Tony D. Davis, Joshua C. Corpuz, Michael D. Burkart
, Nat. Prod. Rep.
, 2020
, 37
, 355
- Combining flavin photocatalysis with parallel synthesis: a general platform to optimize peptides with non-proteinogenic amino acids. Jacob R. Immel, Maheshwerreddy Chilamari, Steven Bloom
, Chem. Sci.
, 2021
, 12
, 10083
- Polymer-coated quantum dots. Nikodem Tomczak, Rongrong Liu, Julius G. Vancso
, Nanoscale
, 2013
, 5
, 12018
- Amino-acids and peptides. Part XXXVII. Trifluoroacetylation during the coupling of t-butoxycarbonylamino-acids with peptide esters in the presence of trifluoroacetate anion. George A. Fletcher, Miklos Löw, Geoffrey T. Young
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 1162
- The use of a macroreticular ion-exchange resin in the isolation stage of the picolyl ester method of peptide synthesis. J. Burton, G. A. Fletcher, G. T. Young
, J. Chem. Soc. D
, 1971
, 1057