Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Xing-Zhong Liu"'
Autor:
Ming-Jun Chen, López-Juan Chavez, Jin-Yuan Kang, Jiang-Xin Hu, Jian-Fei Dong, You-Jiu Tan, Zhu-An Chen, Bo Huang, Chun-Ru Li, Chang-Sheng Sun, Nigel Hywel-Jones, Xing-Zhong Liu, Zeng-Zhi Li
Publikováno v:
Mycology, Pp 1-12 (2024)
ABSTRACTMacro- and microscopic morphological studies and multilocus phylogenetic analysis were made on larval specimens of a ghost moth collected from a pigeon pea plantation in Huánuco, Peru. DNA sequences from the cadaver and the fungal isolates o
Externí odkaz:
https://doaj.org/article/d5576ee0aabd46f4af9c5f530c8bb2c6
Publikováno v:
Molecules, Vol 19, Iss 12, Pp 20880-20887 (2014)
Two new coumarins, talacoumarins A (1) and B (2), were isolated from the ethyl acetate extract of the wetland soil-derived fungus Talaromyces flavus BYD07-13. Their structures were elucidated by spectroscopic data (NMR, MS) analyses. The absolute con
Externí odkaz:
https://doaj.org/article/bedd8c79802e4f00a2d1a9e0df9c882c
Autor:
Tian-Yu Sun, Run-Qiao Kuang, Guo-Dong Chen, Sheng-Ying Qin, Chuan-Xi Wang, Dan Hu, Bing Wu, Xing-Zhong Liu, Xin-Sheng Yao, Hao Gao
Publikováno v:
Molecules, Vol 21, Iss 9, p 1184 (2016)
Three pairs of new isopentenyl dibenzo[b,e]oxepinone enantiomers, (+)-(5S)-arugosin K (1a), (−)-(5R)-arugosin K (1b), (+)-(5S)-arugosin L (2a), (−)-(5R)-arugosin L (2b), (+)-(5S)-arugosin M (3a), (−)-(5R)-arugosin M (3b), and a new isopentenyl
Externí odkaz:
https://doaj.org/article/a67651ee0c3048c7bab2e25444fe984c
Autor:
Kevin D. Hyde, Sinang Hongsanan, Rajesh Jeewon, D. Jayarama Bhat, Eric H. C. McKenzie, E. B. Gareth Jones, Rungtiwa Phookamsak, Hiran A. Ariyawansa, Saranyaphat Boonmee, Qi Zhao, Faten Awad Abdel-Aziz, Mohamed A. Abdel-Wahab, Supharat Banmai, Putarak Chomnunti, Bao-Kai Cui, Dinushani A. Daranagama, Kanad Das, Monika C. Dayarathne, Nimali I. de Silva, Asha J. Dissanayake, Mingkwan Doilom, Anusha H. Ekanayaka, Tatiana Baptista Gibertoni, Aristóteles Góes-Neto, Shi-Ke Huang, Subashini C. Jayasiri, Ruvishika S. Jayawardena, Sirinapa Konta, Hyang Burm Lee, Wen-Jing Li, Chuan-Gen Lin, Jian-Kui Liu, Yong-Zhong Lu, Zong-Long Luo, Ishara S. Manawasinghe, Patinjareveettil Manimohan, Ausana Mapook, Tuula Niskanen, Chada Norphanphoun, Moslem Papizadeh, Rekhani H. Perera, Chayanard Phukhamsakda, Christian Richter, André L. C. M. de A. Santiago, E. Ricardo Drechsler-Santos, Indunil C. Senanayake, Kazuaki Tanaka, T. M. D. S. Tennakoon, Kasun M. Thambugala, Qing Tian, Saowaluck Tibpromma, Benjarong Thongbai, Alfredo Vizzini, Dhanushka N. Wanasinghe, Nalin N. Wijayawardene, Hai-Xia Wu, Jing Yang, Xiang-Yu Zeng, Huang Zhang, Jin-Feng Zhang, Timur S. Bulgakov, Erio Camporesi, Ali H. Bahkali, Mohammad A. Amoozegar, Lidia Silva Araujo-Neta, Joseph F. Ammirati, Abhishek Baghela, R. P. Bhatt, Dimitar Bojantchev, Bart Buyck, Gladstone Alves da Silva, Catarina Letícia Ferreira de Lima, Rafael José Vilela de Oliveira, Carlos Alberto Fragoso de Souza, Yu-Cheng Dai, Bálint Dima, Tham Thi Duong, Enrico Ercole, Fernando Mafalda-Freire, Aniket Ghosh, Akira Hashimoto, Sutakorn Kamolhan, Ji-Chuan Kang, Samantha C. Karunarathna, Paul M. Kirk, Ilkka Kytövuori, Angela Lantieri, Kare Liimatainen, Zuo-Yi Liu, Xing-Zhong Liu, Robert Lücking, Gianfranco Medardi, Peter E. Mortimer, Thi Thuong Thuong Nguyen, Itthayakorn Promputtha, K. N. Anil Raj, Mateus A. Reck, Saisamorn Lumyong, Seyed Abolhassan Shahzadeh-Fazeli, Marc Stadler, Mohammad Reza Soudi, Hong-Yan Su, Takumasa Takahashi, Narumon Tangthirasunun, Priyanka Uniyal, Yong Wang, Ting-Chi Wen, Jian-Chu Xu, Zhong-Kai Zhang, Yong-Chang Zhao, Jun-Liang Zhou, Lin Zhu
Publikováno v:
Fungal Diversity. 80:1-270
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e5943c952fea7534dd6bb35d2245194
https://doi.org/10.1007/s13225-016-0373-x
https://doi.org/10.1007/s13225-016-0373-x
Publikováno v:
Mycoscience (Springer Nature). Jul2009, Vol. 50 Issue 4, p317-321. 5p. 5 Charts.
Publikováno v:
Canadian Journal of Botany. May2003, Vol. 81 Issue 5, p452. 5p. 1 Black and White Photograph, 1 Diagram.
Autor:
Jia Dong Yu, Xing Zhong Liu, De Bing Li, Cong Yun Shi, Wen Jing Chen, Fei Lou, Ying Zhou, Lin Wu, Meng Cheng Yang, Yan Yang
Publikováno v:
Advanced Materials Research. :140-143
A detailed singlet potential energy surface survey on the 1CF2 + 3O2 reaction is carried out in order to clarify the reaction mechanisms of the singlet difluorocarbene (1CF2) with oxygen (3O2) at the B3LYP/6-311++G(d,p) level. To determine the accura
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31a005f845b28aeb7a5d29bc5683fe0a
https://doi.org/10.4028/www.scientific.net/amr.641-642.140
https://doi.org/10.4028/www.scientific.net/amr.641-642.140
Publikováno v:
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 40(17)
Two new polyesters, talapolyesters G-H (1-2) were isolated from the wetland soil-derived fungus Talaromyces flavus BYD07-13, and their structures were determined by NMR and MS spectroscopic data. The absolute configurations of the residues were deter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::750637163ffd85b7e46de4848996c118
https://pubmed.ncbi.nlm.nih.gov/26978970
https://pubmed.ncbi.nlm.nih.gov/26978970
Publikováno v:
Advanced Materials Research. :2438-2442
The mechanism of the reaction of the monobromocarbene (1CHBr) with 3O2 was studied theoretically at the B3LYP/6-311++G(d,p) level on the singlet potential energy surface (PES). All structures of the stationary points (reactants, intermediates, transi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc3485d19eecb214568ad979b48ef0d7
https://doi.org/10.4028/www.scientific.net/amr.396-398.2438
https://doi.org/10.4028/www.scientific.net/amr.396-398.2438
Publikováno v:
Advanced Materials Research. :20-24
Subscript textIn order to clarify the reaction mechanisms of the singlet monochlorocarbene radical (1 CHCl) with 3O2 on the singlet potential energy surface (PES), a detailed theoretical study was carried out at the B3LYP/6-311++G(d,p) level. It is f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e95e20a136a3f6d49865ac689dbfda36
https://doi.org/10.4028/www.scientific.net/amr.356-360.20
https://doi.org/10.4028/www.scientific.net/amr.356-360.20