Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Laxmaiah, Vasamsetty"'
Autor:
Laxmaiah Vasamsetty, Jun Wang
Publikováno v:
Handbook of CH-Functionalization. :1-26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65aab815863130d34a9109bff46af503
https://doi.org/10.1002/9783527834242.chf0025
https://doi.org/10.1002/9783527834242.chf0025
Publikováno v:
Chemistry – A European Journal. 26:14546-14550
A new class of C2 -symmetric, chiral cyclopentadienyl ligand based on planar chiral ferrocene backbone was developed. A series of its corresponding rhodium(I), iridium(I), and ruthenium(II) complexes were prepared as well. In addition, the rhodium(I)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ebd14eb256ec84af9ccebbbf1b29efc
https://doi.org/10.1002/chem.202001814
https://doi.org/10.1002/chem.202001814
Autor:
Weici Xu, Jinggong Liu, Shuang Yang, Sakkani Nagaraju, Xinqiang Fang, Laxmaiah Vasamsetty, Muhammad Naeem Anwar, Jian Liu
Publikováno v:
ACS Catalysis. 10:2882-2893
Developing a catalytic kinetic resolution (KR) protocol affording enantioenriched α-functionalized ketones with broad substrate scope and high efficiency has been a longstanding challenge. Here, we...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c99130088d6ed0ed2f89d8b49147c9d
https://doi.org/10.1021/acscatal.9b05608
https://doi.org/10.1021/acscatal.9b05608
Publikováno v:
Angewandte Chemie. 132:3503-3507
A ruthenium(II)-catalyzed asymmetric intramolecular hydroarylation assisted by a chiral transient directing group has been developed. A series of 2,3-dihydrobenzofurans bearing chiral all-carbon quaternary stereocenters have been prepared in remarkab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29d575f1c9656a3b7399ece50c3732a8
https://doi.org/10.1002/ange.201913733
https://doi.org/10.1002/ange.201913733
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 26(64)
A new class of C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9072765b00fd44db8c3c4bedb748ffcd
https://pubmed.ncbi.nlm.nih.gov/32470226
https://pubmed.ncbi.nlm.nih.gov/32470226
Autor:
Laxmaiah Vasamsetty, Miao Meng, Pogula Sreekanth Reddy, Xinqiang Fang, Xiangwen Kong, Shuang Yang, Weici Xu
Publikováno v:
Chemistry, an Asian journal. 13(24)
Racemic mixtures of four stereoisomers are easily formed via many fundamental organic transformations, but the direct utilities of these mixtures have been less studied and remain large challenges to date. In this work, we introduce a new method, i.e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56f7f154bd3521bd596eabbfb99190b3
https://pubmed.ncbi.nlm.nih.gov/30303309
https://pubmed.ncbi.nlm.nih.gov/30303309
Autor:
Fang Yu, Xiaozhi Liu, Xinqiang Fang, Laxmaiah Vasamsetty, Shuang Yang, Jian Liu, Shuhua Liu, Xiangwen Kong
Publikováno v:
The Journal of organic chemistry. 83(16)
We report that α-acyloxy-β,γ-unsaturated cyclopentenones were used as starting substrates to make various trisubstituted cyclopentadienones. The substrates are easily available in one step from our previously developed protocol, and the potential
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b83962dc0d35447533bda78935e79e2
https://pubmed.ncbi.nlm.nih.gov/29975528
https://pubmed.ncbi.nlm.nih.gov/29975528
Publikováno v:
Tetrahedron. 71:3209-3215
An efficient and versatile synthesis of 3-alkenylbutenolides through direct Suzuki–Miyaura cross coupling reaction between preformed 3-halobutenolides and a range of readily accessible boronic acids has been devised. The coupling process exhibits g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef7f2364dbddf4347a7e399449169064
https://doi.org/10.1016/j.tet.2015.04.009
https://doi.org/10.1016/j.tet.2015.04.009
Publikováno v:
Tetrahedron Letters. 55:7068-7071
A macrocyclic furanobutenolide was crafted from readily available furan building-blocks to set-up a transannular Diels–Alder reaction which delivered the carbocyclic core present in a class of cembranoid diterpene natural products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d46a6c3218cb13f53847360e06d67943
https://doi.org/10.1016/j.tetlet.2014.10.141
https://doi.org/10.1016/j.tetlet.2014.10.141
Publikováno v:
Tetrahedron. 70:8488-8497
A short and generally applicable synthesis of bioactive tetracyclic natural product paracaseolide A has been accomplished employing a ‘proposed’ biomimetic Diels–Alder reaction as the key strategic step. The Diels–Alder precursors for this pu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce038fb946cdb4d7a359ec9aec30b967
https://doi.org/10.1016/j.tet.2014.09.072
https://doi.org/10.1016/j.tet.2014.09.072