Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kurhade Suresh Eknath"'
Publikováno v:
Angew Chem Int Ed Engl
An engineered cyanovirin-N homolog that exhibits specificity for high mannose N-glycans has been constructed to aid type I α-1,2-mannosidase inhibitor discovery and development. Engineering the lectins C-terminus permitted facile functionalization w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77b9297a75389daf31ff8873e568e2c0
https://pubmed.ncbi.nlm.nih.gov/33728787
https://pubmed.ncbi.nlm.nih.gov/33728787
Publikováno v:
Synthesis. 45:1689-1692
The synthesis of a recently identified and highly active sex pheromone of the longtailed mealybug, Pseudococcus longispinus is reported. A concise synthetic route, use of the under explored Meyer–Schuster rearrangement, Claisen rearrangement, and r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::580c85e01051f629de476ed665c2fa7e
https://doi.org/10.1055/s-0033-1338450
https://doi.org/10.1055/s-0033-1338450
Autor:
Madhav S. Mane, Dipak Harel, Bhavana Kardile, Sandip Gavade, Kamlesh Padiya, Shaji Varghese, Vivek S. Gaware, Manojkumar Tiwari, Swapnil Ramesh Bajare, Kurhade Suresh Eknath
Publikováno v:
Organic Letters. 14:2814-2817
The first "In Water" imidazolecarbonylation of amine is described. A one pot reaction of carbonylimidazolide in water with a nucleophile provides an efficient and general method for the preparation of urea, carbamates and thiocarbamates. Use of an an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19e6222be42d0a105adea6f982ee7bd8
https://doi.org/10.1021/ol301009d
https://doi.org/10.1021/ol301009d
Autor:
Salunkhe Videsh, Debnath Bhuniya, Kurhade Suresh Eknath, Vidavalur Siddaiah, D. Srinivasa Reddy
Publikováno v:
Synthesis. 2011:3523-3529
An efficient and convenient method was developed for the synthesis of novel 1,4-oxazepine- and 1,5-oxazocine-based sugar hybrids from readily available deoxysugar azides by means of tributylphosphine-mediated tandem reactions. The resulting glycoconj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0bff46e08ba1fe81d8de8c901f9e778d
https://doi.org/10.1055/s-0030-1260218
https://doi.org/10.1055/s-0030-1260218
Autor:
D. Srinivasa Reddy, Vidavalur Siddaiah, Debnath Bhuniya, Sudhir Ravula, Kurhade Suresh Eknath
Publikováno v:
Tetrahedron Letters. 52:4313-4315
A convenient one-step method for the synthesis of novel dihydrooxazine and oxazoline based sugar hybrids is reported starting from the readily accessible sugar azides and aldehydes. We have used Aube’s protocol to achieve this transformation. The r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5acfa7bd73805aa86818e536016d3bfc
https://doi.org/10.1016/j.tetlet.2011.06.035
https://doi.org/10.1016/j.tetlet.2011.06.035
Autor:
Salunkhe Videsh, D. Srinivasa Reddy, Kurhade Suresh Eknath, Vidavalur Siddaiah, Debnath Bhuniya
Publikováno v:
ChemInform. 43
An efficient and convenient method was developed for the synthesis of novel 1,4-oxazepine- and 1,5-oxazocine-based sugar hybrids from readily available deoxysugar azides by means of tributylphosphine-mediated tandem reactions. The resulting glycoconj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4ed9587f9ff9191b685459f646f0677
https://doi.org/10.1002/chin.201211188
https://doi.org/10.1002/chin.201211188
Autor:
Abbas Sanchawala, Debnath Bhuniya, D. Srinivasa Reddy, Velayutham Ravikumar, Kurhade Suresh Eknath
Publikováno v:
Organic letters. 13(14)
The first total synthesis of isofregenedadiol, a bicyclic diterpene isolated from H. Viscosum, is reported starting from a d-(−)-pantolactone chiral pool. A one-pot quadruple reaction sequence comprising an enyne ring-closing metathesis/cross-metat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f5dc3cb93ece08eff15ed1be77a7de9
https://pubmed.ncbi.nlm.nih.gov/21699171
https://pubmed.ncbi.nlm.nih.gov/21699171
Autor:
D. Srinivasa Reddy, Tanaji Mengawade, Venkata P. Palle, Kurhade Suresh Eknath, Debnath Bhuniya
Publikováno v:
Organicbiomolecular chemistry. 9(3)
An efficient and convenient method for the synthesis of sugar-lactam conjugates is reported starting from readily available sugar azides using the Aube reaction. Cyclic azido alcohols are used in the Aube reaction for the first time in a carbohydrate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccdc5a0f8df4d0eb9036110c8fdcd1ce
https://pubmed.ncbi.nlm.nih.gov/21082141
https://pubmed.ncbi.nlm.nih.gov/21082141