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- Crystallographic characterization of the conformation of the 1-aminocyclohexane-1-carboxylic acid residue in simple derivatives and peptides. Giovanni Valle, Marco Crisma, Claudio Toniolo, Nirupa Sen, Muppalla Sukumar, Padmanabhan Balaram
, J. Chem. Soc., Perkin Trans. 2
, 1988
, 393
- Comparison of heme and nonheme iron-based 1-aminocyclopropane-1-carboxylic acid oxidase mimics: kinetic, mechanistic and computational studies. Dóra Lakk-Bogáth, Gábor Speier, Mihai Surducan, Radu Silaghi-Dumitrescu, A. Jalila Simaan, Bruno Faure, József Kaizer
, RSC Adv.
, 2015
, 5
, 2075
- Amino acid fluorides: viable tools for synthesis of peptides, peptidomimetics and enantiopure heterocycles. Girish Prabhu, N. Narendra, Basavaprabhu, V. Panduranga, Vommina V. Sureshbabu
, RSC Adv.
, 2015
, 5
, 48331
- 1161. Peptides. Part XVIII. Derivatives of 1-aminocyclohexanecarboxylic acid. G. W. Kenner, J. Preston, R. C. Sheppard
, J. Chem. Soc.
, 1965
, 6239
- Single and multiple peptide γ-turns: literature survey and recent progress. Marco Crisma, Marta De Zotti, Alessandro Moretto, Cristina Peggion, Bruno Drouillat, Karen Wright, François Couty, Claudio Toniolo, Fernando Formaggio
, New J. Chem.
, 2015
, 39
, 3208
- Analysis of designed β-hairpin peptides: molecular conformation and packing in crystals. Subrayashastry Aravinda, Upadhyayula S. Raghavender, Rajkishor Rai, Veldore V. Harini, Narayanaswamy Shamala, Padmanabhan Balaram
, Org. Biomol. Chem.
, 2013
, 11
, 4220
- Tripeptide based super-organogelators: structure and function. Debasish Podder, Srayoshi Roy Chowdhury, Sujay Kumar Nandi, Debasish Haldar
, New J. Chem.
, 2019
, 43
, 3743
- Peptide backbone folding induced by the C
α-tetrasubstituted cyclic α-amino acids 4-amino-1,2-dithiolane-4-carboxylic acid (Adt) and 1-aminocyclopentane-1-carboxylic acid (Ac5c). A joint computational and experimental study. Massimiliano Aschi, Gino Lucente, Fernando Mazza, Adriano Mollica, Enrico Morera, Marianna Nalli, Mario Paglialunga Paradisi
, Org. Biomol. Chem.
, 2003
, 1
, 1980
- Utilization of achiral alkenyl amines for the preparation of high affinity Grb2 SH2 domain-binding macrocycles by ring-closing metathesis. Fa Liu, Karen M. Worthy, Lakshman Bindu, Alessio Giubellino, Donald P. Bottaro, Robert J. Fisher, Terrence R. Burke Jr.
, Org. Biomol. Chem.
, 2007
, 5
, 367
- 29. Triad prototropic systems. Part I. The mobility of the azomethine system during decarboxylation. Fawzy G. Baddar
, J. Chem. Soc.
, 1950
, 136