Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Venkateswara Rao, Batchu"'
Autor:
Siva Krishna, Jattuboyina, Bharathkumar, Hanumantharayappa, Nalla, Saikumar, Chirke, Sahadev S, Basetty, Shalini, Racha, Vyshnavi, Kumaraguru, Thenkrishnan, Amanchy, Ramars, Venkateswara Rao, Batchu
Publikováno v:
In Results in Chemistry December 2023 6
Autor:
Hanumantharayappa Bharathkumar, Jattuboyina Siva Krishna, Banothu Surender, Venkateswara Rao Batchu
Publikováno v:
SynOpen, Vol 06, Iss 04, Pp 238-257 (2022)
This review reports on the total synthesis of conduramines, which are formally derived from conduritols, mainly containing a trihydroxy aminocyclohexene core. Analysis of the different strategies developed to prepare these aminocyclohexene triols and
Externí odkaz:
https://doaj.org/article/2b399eec158041ddb42d3f6d1b4d39ca
Publikováno v:
In Carbohydrate Research November 2021 509
Autor:
Venkateswara Rao Batchu, Jattuboyina Siva Krishna, Hanumantharayappa Bharathkumar, Banothu Surender
Publikováno v:
SynOpen. :238-257
This review reports on the total synthesis of conduramines, which are formally derived from conduritols, mainly containing a trihydroxy aminocyclohexene core. Analysis of the different strategies developed to prepare these aminocyclohexene triols and
Autor:
Naresh, Annavareddi, Venkateswara Rao, Maddimsetti, Kotapalli, Sudha Sravanti, Ummanni, Ramesh, Venkateswara Rao, Batchu
Publikováno v:
In European Journal of Medicinal Chemistry 10 June 2014 80:295-307
Publikováno v:
In Tetrahedron: Asymmetry 15 May 2012 23(9):697-702
Publikováno v:
In Tetrahedron: Asymmetry 30 April 2012 23(8):564-569
Publikováno v:
Tetrahedron Letters. 58:559-562
A short and stereoselective synthesis of conduramine F-1 and ent- conduramine E-1 derivatives have been achieved starting from d -mannitol using nucleophilic vinylation on imine. A concise sequence of vinylation at both ends of d -mannitol and follow
Publikováno v:
Tetrahedron Letters. 58:563-565
A simple and an efficient strategy have been developed for the stereoselective synthesis of peracetylated (−)-gloeosporiol by acid catalysed cyclisation from the commercially available starting materials.
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 5, Iss 1, p 64 (2009)
Pd/C-mediated alkynylation of 5-iodo-pyrazole-4-carboxylic acid, involving the first regioselective construction of α-pyrone ring on a pyrazol moiety via tandem coupling–cyclization process, has been developed to afford pyrano[4,3-c]pyrazol-4(1H)-
Externí odkaz:
https://doaj.org/article/03f059c4acf1450e8e6c650a0f60ab06