Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hongxiu Huang"'
Publikováno v:
Angewandte Chemie (International ed. in English). 59(52)
The first total synthesis of liangshanone, a hexacyclic ent-kaurane diterpenoid alkaloid, has been completed. Its intricate cagelike framework was assembled through several key transformations, including an oxidative dearomatization/Diels-Alder (OD/D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4470f2d8a292cb9cb20bba123ef7dcfc
https://pubmed.ncbi.nlm.nih.gov/32902096
https://pubmed.ncbi.nlm.nih.gov/32902096
Publikováno v:
Chemistry - A European Journal. 21:13284-13290
The bioactive Kopsia alkaloids lundurines A-D are the only natural products known to contain indolylcyclopropane. Achieving their syntheses can provide important insights into their biogenesis, as well as novel synthetic routes for complex natural pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55128a6910e93fcd196989860b834bdf
https://doi.org/10.1002/chem.201502011
https://doi.org/10.1002/chem.201502011
Autor:
Shuqing Wang, Dan Zhang, Ling Tan, Yong Qin, Pei Tang, Hao Song, Hui-Jing Wang, Hongxiu Huang, Xiao-Yu Liu
Publikováno v:
The Journal of organic chemistry. 81(21)
A highly diastereoselective Michael addition of (R)-N-tert-butanesulfinyl imidates 8 to α,β-unsaturated pyrazolidinone 3a has been developed to afford pyrazolidinones 10 possessing three contiguous stereocenters with good to excellent yield and exc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b719dd61042734a37451367b30efd84e
https://pubmed.ncbi.nlm.nih.gov/27439016
https://pubmed.ncbi.nlm.nih.gov/27439016
Publikováno v:
ChemInform. 46
Total syntheses of (-)-isoschizogamine and (-)-2-hydroxyisoschizogamine are described. The synthesis employs two asymmetric Michael additions to establish chiral centers at C7 and the quaternary carbon C20. Regioselective reduction of the methylthioi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e720df14fd2816481959f842c1eccb0
https://doi.org/10.1002/chin.201548196
https://doi.org/10.1002/chin.201548196
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 21(41)
Total syntheses of (-)-isoschizogamine and (-)-2-hydroxyisoschizogamine are described. The synthesis employs two asymmetric Michael additions to establish chiral centers at C7 and the quaternary carbon C20. Regioselective reduction of the methylthioi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a2463587d3e836edf0d37465cf0b3c2
https://pubmed.ncbi.nlm.nih.gov/26291890
https://pubmed.ncbi.nlm.nih.gov/26291890
Publikováno v:
ChemInform. 46
Imidates (I) or (IV) and α,β-unsaturated diesters are subjected to a one-pot, three-step cascade reaction to afford the desired lactone structures in a completely diastereoselective manner.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95a03bcd091fedf079ce776ee3932e7c
https://doi.org/10.1002/chin.201529140
https://doi.org/10.1002/chin.201529140
Publikováno v:
The Journal of organic chemistry. 80(5)
Multisubstituted chiral butyrolactonimidates have been synthesized via a one-pot, three-step cascade reaction in which (R)-N-tert-butanesulfinyl imidates and α,β-unsaturated diesters undergo highly stereoselective Michael addition, anion-oxidative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4228376a8ad3aa9986d35d72b130746
https://pubmed.ncbi.nlm.nih.gov/25671631
https://pubmed.ncbi.nlm.nih.gov/25671631
Publikováno v:
Journal of Organic Chemistry; 3/6/2015, Vol. 80 Issue 5, p2494-2502, 9p