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pro vyhledávání: '"Chinthaginjala Srinivasulu"'
Autor:
Chinthaginjala Srinivasulu, Nagamangala R. Sagar, Thimmalapura M. Vishwanatha, Suram Durgamma, Vommina V. Sureshbabu
Publikováno v:
ACS Omega, Vol 6, Iss 7, Pp 4680-4686 (2021)
Externí odkaz:
https://doaj.org/article/9cd726b07dae4c95a83f4c4f404fa32e
Akademický článek
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Autor:
Chinthaginjala, Srinivasulu1 (AUTHOR), Alavandimat, Nanda H.1 (AUTHOR), Umesha, Vathsala1 (AUTHOR), Sureshbabu, Vommina V.1 (AUTHOR)
Publikováno v:
Synthetic Communications. 2021, Vol. 51 Issue 19, p2975-2983. 9p. 1 Black and White Photograph, 2 Graphs.
Autor:
Chinthaginjala, Srinivasulu1 (AUTHOR), Kuppi Reddy Gari, Divya1 (AUTHOR), Nagamangala Ramachandra, Sagar1 (AUTHOR), Sureshbabu, Vommina V.1 (AUTHOR) sureshbabuvommina@rediffmail.com
Publikováno v:
Synthetic Communications. 2020, Vol. 50 Issue 14, p2171-2180. 10p. 4 Diagrams, 1 Chart.
An efficient and facile method has been developed for the synthesis of chiral ��-amino bromides from their corresponding alcohols under Appel reaction conditions. This approach allows for the deoxybromination of a variety of ��-amino alcohols
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29f8d9a43620c3c9b716110bae721d09
Autor:
Chinthaginjala, Srinivasulu, Nagamangala R, Sagar, Thimmalapura M, Vishwanatha, Suram, Durgamma, Vommina V, Sureshbabu
Publikováno v:
ACS Omega
Chiral amino acid-derived formamides represent one of the most versatile components in multicomponent reactions. Herein, we describe a facile synthesis of Nβ-protected amino sulfenyl methyl formamides and sulfonyl methyl formamides via the Mannich r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::19a538778e2fcaebcb67aa41f2bc1f73
https://pubmed.ncbi.nlm.nih.gov/33644575
https://pubmed.ncbi.nlm.nih.gov/33644575