Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Chung Whan Lee"'
Autor:
Han‐Eol Park, Song Hyun Jo, Rosalind H. Lee, Christian P. Macks, Taeyun Ku, Jihwan Park, Chung Whan Lee, Junho K. Hur, Chang Ho Sohn
Publikováno v:
Advanced Science, Vol 10, Iss 16, Pp n/a-n/a (2023)
Abstract Spatial transcriptomics is a newly emerging field that enables high‐throughput investigation of the spatial localization of transcripts and related analyses in various applications for biological systems. By transitioning from conventional
Externí odkaz:
https://doaj.org/article/0d314c6b20064328a975ad772c270f0c
Publikováno v:
Polymer Chemistry. 13:5177-5187
This review presents the recent progress in multi-chromic polymers embedded with mechanophores concentrating on transduction mechanisms and design concepts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ae50e600cef533210bf44288f8e56d2
https://doi.org/10.1039/d2py00435f
https://doi.org/10.1039/d2py00435f
Publikováno v:
European Journal of Organic Chemistry. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdca3912420d96459235b21bfdaab8bb
https://doi.org/10.1002/ejoc.202201286
https://doi.org/10.1002/ejoc.202201286
Publikováno v:
Organic letters. 21(23)
We report our iterative efforts toward the divergent total syntheses of curcusones A–D via Suzuki coupling, intramolecular cyclopropanation, and a key divinylcyclopropane rearrangement. Progress of our synthesis was repeatedly challenged by the hig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a10da0b11f26cbc543b3727b5dd305d8
https://pubmed.ncbi.nlm.nih.gov/31763859
https://pubmed.ncbi.nlm.nih.gov/31763859
Autor:
Buck L. H. Taylor, Keiji Morokuma, Ashay Patel, Brian M. Stoltz, K. N. Houk, Chung Whan Lee, Galina P. Petrova
In the course of a total synthesis effort directed toward the natural product curcusone C, the Stoltz group discovered an unexpected thermal rearrangement of a divinylcyclopropane to the product of a formal Cope/1,3-sigmatropic shift sequence. Since
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0e50eba6095806e80d49ca070017b9c
https://resolver.caltech.edu/CaltechAUTHORS:20190325-131628168
https://resolver.caltech.edu/CaltechAUTHORS:20190325-131628168
Publikováno v:
ChemInform. 46
An improved method for the asymmetric alkylation of 3-bromooxindoles with α-arylated malonate esters is described. The asymmetric alkylation demonstrated was achieved up to 70% ee utilizing a copper(II) bis(phosphine) complex.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7207f6f616ddcb37af8b9f9d247af84
https://doi.org/10.1002/chin.201537142
https://doi.org/10.1002/chin.201537142
Publikováno v:
Organic Letters; Dec2019, Vol. 21 Issue 23, p9658-9662, 5p
An improved method for the asymmetric alkylation of 3-bromooxindoles with α-arylated malonate esters is described. The asymmetric alkylation demonstrated was achieved up to 70% ee utilizing a copper(II) bis(phosphine) complex.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7876580b7c7d52b31785080ce426fea2
https://europepmc.org/articles/PMC4429905/
https://europepmc.org/articles/PMC4429905/
Publikováno v:
ChemInform. 42
A terminal alkyne, a vinyl ketone or an acrylate, and water undergo react in the presence of RUP to give the desired 1,4-diketones with some exceptions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::705e2acd100de6794b39d9e545d36d08
https://doi.org/10.1002/chin.201151059
https://doi.org/10.1002/chin.201151059
Publikováno v:
Chemistry, an Asian journal. 6(8)
A terminal alkyne, a vinyl ketone or an acrylate, and water undergo react in the presence of RUP to give the desired 1,4-diketones with some exceptions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cab98822c2877fbb9cc89c8aff4c4183
https://pubmed.ncbi.nlm.nih.gov/21688397
https://pubmed.ncbi.nlm.nih.gov/21688397