Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ravuri, Srinath"'
Autor:
Saswati Adhikary, Leena Majumder, Sourav Pakrashy, Ravuri Srinath, Kaustuv Mukherjee, Chitra Mandal, Biswadip Banerji
Publikováno v:
ACS Omega, Vol 5, Iss 24, Pp 14394-14407 (2020)
Externí odkaz:
https://doaj.org/article/d783752b0d124a108928bf9eadbeac41
Autor:
Vinothkumar Vinayagam, Satish Kumar Karre, Sreenivasa Reddy Kasu, Ravuri Srinath, Hema Sundar Naveen Babu Bathula, Subir Kumar Sadhukhan
Publikováno v:
Organic Letters. 24:6142-6147
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bb9f40b78bada4fc8d2dc5d01173de3
https://doi.org/10.1021/acs.orglett.2c02231
https://doi.org/10.1021/acs.orglett.2c02231
Autor:
Nakul C. Maiti, Subhankar Shee, Biswadip Banerji, Saswati Ghosh, Arindam Manna, Ravuri Srinath, Krishnendu Khamaru, Vijay Babu Pathi
Publikováno v:
Organic Letters. 23:9365-9370
Herein, a one-pot protocol to synthesize tetracyclic triazole-piperazine-quinazolinone-fused N-heterocyclic scaffolds is reported. In this strategy, a tandem approach of two highly efficient synthetic reactions, click and cross-dehydrogentive couplin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5b9ea757abb450d65b53f880963fd21
https://doi.org/10.1021/acs.orglett.1c03435
https://doi.org/10.1021/acs.orglett.1c03435
Autor:
Vinothkumar, Vinayagam, Satish Kumar, Karre, Sreenivasa Reddy, Kasu, Ravuri, Srinath, Hema Sundar, Naveen Babu Bathula, Subir Kumar, Sadhukhan
Publikováno v:
Organic letters. 24(33)
Herein, we report for the first time a transition-metal-free frustrated Lewis pair (FLP) catalyzed CHF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c1a00f1e877bdc532245d4b00a093a7d
https://pubmed.ncbi.nlm.nih.gov/35938941
https://pubmed.ncbi.nlm.nih.gov/35938941
Autor:
Ravuri Srinath, Kaustuv Mukherjee, Saswati Adhikary, Sourav Pakrashy, Leena Majumder, Biswadip Banerji, Chitra Mandal
Publikováno v:
ACS Omega, Vol 5, Iss 24, Pp 14394-14407 (2020)
An iodine-catalyzed, environmentally benign one-pot methodology has been developed for the synthesis of diverse substituted imidazoles. This transition-metal-free, aerobic, water-mediated cyclization reaction is operationally simple and works well wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b511dfad9ce5871b91e96d284a20ab59
https://doi.org/10.1021/acsomega.0c00934
https://doi.org/10.1021/acsomega.0c00934
Autor:
Ravuri Srinath, Satadru Chatterjee, Afifa Rahman, Krishnendu Khamaru, Suvankar Bera, Biswadip Banerji
Publikováno v:
Organic Letters. 21:9028-9032
A modular strategy to obtain three different products from a single substrate was developed. The present methodology unveils new step-economical and cost-efficient routes to access diverse fused qu...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::922140a4beeac450942f2c410d97af1e
https://doi.org/10.1021/acs.orglett.9b03428
https://doi.org/10.1021/acs.orglett.9b03428
Akademický článek
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Autor:
Satadru, Chatterjee, Ravuri, Srinath, Suvankar, Bera, Krishnendu, Khamaru, Afifa, Rahman, Biswadip, Banerji
Publikováno v:
Organic letters. 21(22)
A modular strategy to obtain three different products from a single substrate was developed. The present methodology unveils new step-economical and cost-efficient routes to access diverse fused quinazolinoquinazolinone derivatives which are not prev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::724a314f23877958dde4d9f896005bdd
https://pubmed.ncbi.nlm.nih.gov/31680524
https://pubmed.ncbi.nlm.nih.gov/31680524