Zobrazeno 1 - 10
of 58
pro vyhledávání: '"G. Sudhakar Reddy"'
Autor:
G. Sudhakar Reddy, E. J. Corey
Publikováno v:
Organic Letters. 25:3539-3542
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f1b2a220e7ac113d1f14a9ac9a32abf
https://doi.org/10.1021/acs.orglett.3c01123
https://doi.org/10.1021/acs.orglett.3c01123
Autor:
G. Sudhakar Reddy, E. J. Corey
Publikováno v:
Organic Letters. 25:1872-1877
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fea4b4479ff76e49df6ec598a27f142e
https://doi.org/10.1021/acs.orglett.3c00353
https://doi.org/10.1021/acs.orglett.3c00353
Autor:
G. Sudhakar Reddy, E. J. Corey
Publikováno v:
Organic letters.
The mechanistic pathway for the formation of 1,2-oxazetes by reaction of olefins with nitrous anhydride has been clarified. The initial reaction intermediate, a β-nitroso nitrite ester that is sensitive to light, undergoes O-NO fission to form a β-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97e4466bf9d606940419d7456bafd887
https://pubmed.ncbi.nlm.nih.gov/36583698
https://pubmed.ncbi.nlm.nih.gov/36583698
Autor:
G. Sudhakar Reddy, E. J. Corey
Publikováno v:
Organic Letters. 23:3399-3402
Triflyl nitrate is easily generated from tetra-n-butylammonium nitrate in CH2Cl2 solution and serves as an effective nitrating agent for a wide range of unsaturated substrates to form nitro olefins.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b205d2d2b18d0d2bd6b95c8aed89832
https://doi.org/10.1021/acs.orglett.1c00868
https://doi.org/10.1021/acs.orglett.1c00868
Publikováno v:
Organic Letters. 23:2258-2262
Concise stereocontrolled synthetic routes to the C2-symmetric azatetraquinane 1 (or, also, the enantiomer) are described. The successful execution of the synthesis involved innovation in the method...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5af7be1afcb3b05c55731fba9dce010
https://doi.org/10.1021/acs.orglett.1c00387
https://doi.org/10.1021/acs.orglett.1c00387
Publikováno v:
Organic letters. 24(23)
Nitrosyl triflate (TfONO) can be generated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66eabcb0b36213c40028303484945ad8
https://pubmed.ncbi.nlm.nih.gov/35653176
https://pubmed.ncbi.nlm.nih.gov/35653176
Publikováno v:
Organic Letters. 23:5445-5447
A study of [3 + 2] cycloaddition reactions of a bicyclic nitrone with various cyclopentenes has clarified the diastereomeric preferences as a function of the olefinic structure. It has also identified an important stereochemical difference between ni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::970c8985f50204bc7b4d0126990a808d
https://doi.org/10.1021/acs.orglett.1c01787
https://doi.org/10.1021/acs.orglett.1c01787
Autor:
N. Arjunreddy Mallampudi, Birakishore Padhi, Utkal Mani Choudhury, G. Sudhakar Reddy, Debendra K. Mohapatra
Publikováno v:
Organic & Biomolecular Chemistry. 18:2685-2695
An efficient CuBr2-catalyzed diastereoselective allylation of a cyclic hemiacetal with allyltrimethylsilane as a nucleophile has been developed. The protocol offers a cost effective, protecting group tolerant, and operationally simple approach to 2,6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85b5e11d2eb4cf620d10c36dc5919ac3
https://doi.org/10.1039/c9ob02689d
https://doi.org/10.1039/c9ob02689d
Autor:
Kanakaraju Marumudi, Janardhan Gaddam, Debendra K. Mohapatra, Jhillu S. Yadav, G. Sudhakar Reddy, Ajit C. Kunwar
Publikováno v:
Organic & Biomolecular Chemistry. 17:5601-5614
The first asymmetric total synthesis and stereochemical assignments of 10-membered macrolactones relgro and 10'-oxorelgro are disclosed. To this end, palladium-catalyzed Stille coupling, the Mitsunobu reaction, ring-closing metathesis, EDCI promoted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1151f9f74589124440e6de25851675c0
https://doi.org/10.1039/c9ob00838a
https://doi.org/10.1039/c9ob00838a
Publikováno v:
Organic letters. 23(6)
Concise stereocontrolled synthetic routes to the C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a89f99a1326cb370bce1451956b8fab9
https://pubmed.ncbi.nlm.nih.gov/33646796
https://pubmed.ncbi.nlm.nih.gov/33646796