Zobrazeno 1 - 10
of 192
pro vyhledávání: '"Vommina V. Sureshbabu"'
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
Publikováno v:
ARKIVOC, Vol 2018, Iss 7, Pp 449-457 (2018)
Externí odkaz:
https://doaj.org/article/d0ed7cd9c4054b41b7b6cb2dbf956e83
Publikováno v:
ARKIVOC, Vol 2010, Iss 11, Pp 77-90 (2010)
Externí odkaz:
https://doaj.org/article/bb77d5da63c649548dce94e0a6f78d0c
Autor:
Vommina V. Sureshbabu, Hemantha H. P.
Publikováno v:
ARKIVOC, Vol 2008, Iss 2, Pp 243-249 (2008)
Externí odkaz:
https://doaj.org/article/dd22853b5aca4077a626372804d28b45
Publikováno v:
Synthetic Communications. 51:2975-2983
An efficient and facile method has been developed for the synthesis of chiral β-amino bromides from their corresponding alcohols under Appel reaction conditions. This approach allows for the deoxyb...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdb21bfd1082ee4ffc8f03848d7419a0
https://doi.org/10.1080/00397911.2021.1955270
https://doi.org/10.1080/00397911.2021.1955270
Publikováno v:
ACS Omega, Vol 6, Iss 7, Pp 4680-4686 (2021)
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 formami...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78e6dba031ca19a30471f5b8e79a9913
https://doi.org/10.1021/acsomega.0c05419
https://doi.org/10.1021/acsomega.0c05419
Publikováno v:
International Journal of Peptide Research and Therapeutics. 27:497-502
An efficient synthesis of Nα-protected amino nitriles from Nα-protected amino acid amides employing Ph3P, I2 and NMM was described. Various amino acid amides, protected by Fmoc, Z and Boc were conveniently converted to nitriles in high yields. Side
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00f283d883b075afc417d73881aedd98
https://doi.org/10.1007/s10989-020-10101-y
https://doi.org/10.1007/s10989-020-10101-y
Publikováno v:
New Journal of Chemistry. 44:7261-7264
The synthesis of a new class of amino phosphinodiselenoic acid ester and β-amino diselenides is conducted by employing a reaction between Nβ-protected aminoalkyl iodide and phosphorus pentaselenide (P2Se5) has been described. In the presence of pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d50c7fa16a1295f922a57e574305956
https://doi.org/10.1039/d0nj00012d
https://doi.org/10.1039/d0nj00012d
Publikováno v:
ChemistrySelect. 4:6408-6413
Herein we demonstrate a chemoselective reaction of Nβ-protected amino alkyl sulfonyl azides with in situ generated Nα-protected amino acid selenocarboxylates via step wise intramolecular cyclization followed by decomposition to obtain N-acyl sulfon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c539e64baf39d6e28200bdfd6609c05b
https://doi.org/10.1002/slct.201901024
https://doi.org/10.1002/slct.201901024
Publikováno v:
ARKIVOC, Vol 2018, Iss 7, Pp 449-457 (2018)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20efd2f4917ab2b3e9a3fa0246d139ba
https://doi.org/10.24820/ark.5550190.p010.727
https://doi.org/10.24820/ark.5550190.p010.727