REFERENCES

1. Maruoka K, Ito M, Yamamoto H. Unprecedented nucleophilic addition of organolithiums to aromatic aldehydes and ketones by complexation with aluminum tris(2,6-diphenylphenoxide). J Am Chem Soc 1995;117:9091-2.

2. Yamamoto H, Futatsugi K. “Designer acids”: combined acid catalysis for asymmetric synthesis. Angew Chem Int Ed Engl 2005;44:1924-42.

3. Bhadra S, Yamamoto H. Substrate directed asymmetric reactions. Chem Rev 2018;118:3391-446.

4. Sawano T, Yamamoto H. Substrate-directed catalytic selective chemical reactions. J Org Chem 2018;83:4889-904.

5. Isidro-Llobet A, Kenworthy MN, Mukherjee S, et al. Sustainability challenges in peptide synthesis and purification: from R&D to production. J Org Chem 2019;84:4615-28.

6. Tsuji H, Yamamoto H. Hydroxy-directed amidation of carboxylic acid esters using a tantalum alkoxide catalyst. J Am Chem Soc 2016;138:14218-21.

7. Muramatsu W, Hattori T, Yamamoto H. Substrate-directed lewis-acid catalysis for peptide synthesis. J Am Chem Soc 2019;141:12288-95.

8. Muramatsu W, Yamamoto H. Peptide bond formation of amino acids by transient masking with silylating reagents. J Am Chem Soc 2021;143:6792-7.

9. Hattori T, Yamamoto H. Synthesis of silacyclic dipeptides: peptide elongation at both N- and C-termini of dipeptide. J Am Chem Soc 2022;144:1758-65.

10. Yamamoto H. Unpublished.

Chemical Synthesis
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All published articles are preserved here permanently:

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