Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Mukund G. Kulkarni"'
Autor:
Mukund G. Kulkarni, Mayur P. Desai, Deekshaputra R. Birhade, Yunus B. Shaikh, Ajit N. Dhatrak, Ramesh Gannimani
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 1725-1729 (2012)
Efficient syntheses are described for the synthetically important 3-methylquinoline-4-carbaldehydes 6a–h from o-nitrobenzaldehydes 1a–h employing a Wittig-olefination–Claisen-rearrangement protocol. The Wittig reaction of o-nitrobenzaldehydes w
Externí odkaz:
https://doaj.org/article/3198da7c50514e78838a56a03039ce18
Autor:
Mukund G. Kulkarni, Attrimuni P. Dhondge, Sanjay W. Chavhan, Ajit S. Borhade, Yunnus B. Shaikh, Deekshaputra R. Birhade, Mayur P. Desai, Nagorao R. Dhatrak
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 6, Iss 1, Pp 876-879 (2010)
Wittig olefination–Claisen rearrangement protocol was applied to obtain 3-allyl oxindole. This oxindole was then converted to (±)-coerulescine and (±)-horsfiline.
Externí odkaz:
https://doaj.org/article/3426423e3eac4dcf9aa15f4f00d8f82d
Autor:
Mukund G. Kulkarni, Sanjay W. Chavhan, Mahadev P. Shinde, Dnyaneshwar D. Gaikwad, Ajit S. Borhade, Attrimuni P. Dhondge, Yunnus B. Shaikh, Vijay B. Ningdale, Mayur P. Desai, Deekshaputra R. Birhade
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 5, Iss 1, p 4 (2009)
A zeolite-catalyzed, simple, one-pot, solvent-free, cost effective, and environmentally benign process for the synthesis of dihydropyrimidones is described. This reaction is scaleable to multigram scale and the catalyst is recyclable. This methodolog
Externí odkaz:
https://doaj.org/article/ec6a402456bb4308b6ca1a459369c8c0
Publikováno v:
Tetrahedron: Asymmetry. 26:746-750
A successful application of the Wittig-olefination–Claisen rearrangement protocol gave the allyl vinyl ether 12 , which was efficiently converted into (−)-tashiromine alkaloids in a short sequence with high overall yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51e618ec41ff9982839893435807f896
https://doi.org/10.1016/j.tetasy.2015.05.011
https://doi.org/10.1016/j.tetasy.2015.05.011
Autor:
Rangarao Kolla, Mukund G. Kulkarni, Narendra Kumar Tripathy, Chinmoy Pramanik, Srinivasarao Sompalli, Kiran Bapat, Ashok Chaudhari, Mukund K. Gurjar
Publikováno v:
Organic Process Research & Development. 18:495-500
Commercial manufacturing of benzphetamine hydrochloride along with its impurity profiling is disclosed. Deoxygenation of pseudoephedrine is reported with ∼100% retention by shielding the amine group as its tert-butyl carbamate, which is very straig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c985ab92f6dfe27ee0f5789a64ede391
https://doi.org/10.1021/op400313y
https://doi.org/10.1021/op400313y
Autor:
Mukund K. Gurjar, Narendra Kumar Tripathy, Sandeep Kotharkar, Yogesh More, Tushar P. Khaladkar, Balaji Vasant Chaugule, Kaliaperumal Neelakandan, Ashok Chaudhari, Ajit S. Borhade, Mukund G. Kulkarni, Chinmoy Pramanik, Pradip Patil, Dinkar Gotrane
Publikováno v:
Organic Process Research & Development. 18:152-156
A commercially viable manufacturing process for propofol (1) is described. The process avoids acid–base neutralization events during isolation of intermediate, 2,6-di-isopropylbenzoic acid (3) and crude propofol, and thus simplifies the synthesis o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::632cf15dc5d8124ed5277465d1e0dc88
https://doi.org/10.1021/op400300t
https://doi.org/10.1021/op400300t
Autor:
Mukund G. Kulkarni, Viraj A. Bhosale
Publikováno v:
Tetrahedron Letters. 56:2568-2570
An efficient total synthesis of (±) Xyloketal H is described, the Wittig olefination–Claisen rearrangement protocol has served here as the key transformation for constructing the core structure of the metabolite.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b8a64719b08de5cfca95cfa03c50a0f
https://doi.org/10.1016/j.tetlet.2015.03.118
https://doi.org/10.1016/j.tetlet.2015.03.118
Autor:
Yunnus B. Shaikh, Mukund G. Kulkarni, Ajit N Dhatrak, Ramesh Gannimani, Deekshaputra R. Birhade, Mayur P. Desai
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 1725-1729 (2012)
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 1725-1729 (2012)
Efficient syntheses are described for the synthetically important 3-methylquinoline-4-carbaldehydes 6a–h from o-nitrobenzaldehydes 1a–h employing a Wittig-olefination–Claisen-rearrangement protocol. The Wittig reaction of o-nitrobenzaldehydes w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70caf0bb98e56fb9005115c7668cc161
http://europepmc.org/articles/PMC3511006
http://europepmc.org/articles/PMC3511006
Autor:
Nagorao R. Dhatrak, Deekshaputra R. Birhade, Attrimuni P. Dhondge, Ajit S. Borhade, Yunnus B. Shaikh, Sanjay W. Chavhan, Mukund G. Kulkarni, Dnyaneshwar D. Gaikwad
Publikováno v:
Tetrahedron: Asymmetry. 23:1234-1237
The synthesis of (+)-isofagomine 1 using 4-pentenol 3 as a chiral precursor is described herein.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e1b9e126b659558f9892685494d08ac
https://doi.org/10.1016/j.tetasy.2012.08.012
https://doi.org/10.1016/j.tetasy.2012.08.012
Autor:
Deekshaputra R. Birhade, Attrimuni P. Dhondge, Mukund G. Kulkarni, Nagorao R. Dhatrak, Ajit S. Borhade, Yunnus B. Shaikh
Publikováno v:
Tetrahedron Letters. 52:5559-5562
A stereodivergent route, starting from d -glyceraldehyde derivative, employing Wittig olefination–Claisen rearrangement protocol is reported for the synthesis of six novel carbahexofuranoses—carba-α- d -glucofuranose, carba-β- d -altrofuranose,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1233c6149bd8ded138a77013af5454ba
https://doi.org/10.1016/j.tetlet.2011.08.006
https://doi.org/10.1016/j.tetlet.2011.08.006