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1.	Ahmad, T, et al. (author) Global patient outcomes after elective surgery: prospective cohort study in 27 low-, middle- and high-income countries 2016 In: British journal of anaesthesia. - : Elsevier BV. - 1471-6771 .- 0007-0912. ; 117:5, s. 601- Journal article (peer-reviewed)
2.	Ahmad, T, et al. (author) In-hospital clinical outcomes after upper gastrointestinal surgery: Data from an international observational study 2017 In: European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology. - : Elsevier BV. - 1532-2157 .- 0748-7983. ; 43:12, s. 2324-2332 Journal article (peer-reviewed)
3.	Ahmad, T, et al. (author) Use of failure-to-rescue to identify international variation in postoperative care in low-, middle- and high-income countries: a 7-day cohort study of elective surgery 2017 In: British journal of anaesthesia. - : Elsevier BV. - 1471-6771 .- 0007-0912. ; 119:2, s. 258-266 Journal article (peer-reviewed)
4.	Jakobsson, J., et al. (author) Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 2021 In: Autophagy. - : Informa UK Limited. - 1554-8635 .- 1554-8627. ; 17:1, s. 1-382 Journal article (peer-reviewed)
5.	MENG, QS, et al. (author) BORDERLINE SOLVOLYTIC REACTIONS - APPEARANCE OF SOLVENT-PROMOTED E2 REACTION IN COMPETITION WITH STEPWISE ELIMINATION AND SUBSTITUTION-REACTIONS 1995 In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - : AMER CHEMICAL SOC. ; 117:6 Other publication (other academic/artistic)
6.	Meng, QS, et al. (author) Concerted and stepwise solvolytic elimination and substitution reactions: Stereochemistry and substituent effects 1997 In: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 119:6, s. 1217-1223 Journal article (peer-reviewed)abstract Solvolysis of the R,R and R,S isomers 2a-X and 2b-X, respectively, (X = I, Br, OBs) in 25 vol % acetonitrile in water gives the elimination products 4, 5a, and 5b along with the substitution products 2a-OH, 2b-OH, 2a-NHCOMe, and 2b-NHCOMe. The rates of e
7.	Meng, QS, et al. (author) Mechanisms of elimination and substitution reactions. Spontaneous solvolysis reactions via carbanion and carbocation intermediates 1999 In: JOURNAL OF PHYSICAL ORGANIC CHEMISTRY. - : JOHN WILEY & SONS LTD. ; 12:2 Other publication (other academic/artistic)abstract The reactions of 4-(4'-nitrophenyl)-4-X-butan-2-one (1-X; X = Cl, OTs) with added bases/nucleophiles exhibit second-order kinetics. These substitution and elimination reactions are concluded to be of concerted S(N)2 type and irreversible E1cB type, respe
8.	Meng, QS, et al. (author) Mechanisms of solvent- and base-promoted imine-forming elimination reactions 1997 In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - : AMER CHEMICAL SOC. ; 119:6 Other publication (other academic/artistic)abstract Solvolysis of 9-(N-chloro-N-methylamino)fluorene (1-Cl) in 25 vol % acetonitrile in water gives the imine fluorenylidenemethylamine (3) as the sole product. The kinetic deuterium isotope effect was measured with the deuterated analogue (9-H-2)-9-(N-chlor
9.	Meng, QS, et al. (author) Mechanisms of solvolytic elimination reactions of tertiary substrates: stereospecific 1,2-elimination reactions 1999 In: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2. - : ROYAL SOC CHEMISTRY. ; :7 Other publication (other academic/artistic)abstract Solvolysis of(R,S)-1-chloro-1-(fluoren-9-yl)-2-methylcyclopentane (1-Cl) or the analogous 3,5-dinitrobenzoate ester 1-DNB in largely aqueous solutions yields alkenes 1-(fluoren-9-yl)-2-methylcyclopentene (4) and 1-(fluoren-9-yl)-5-methylcyclopentene (5)
10.	Meng, QS, et al. (author) Solvent-promoted E1cB/E2 reactions competing with stepwise solvolysis through homoallylic carbocations 1998 In: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2. - : ROYAL SOC CHEMISTRY. ; :3 Other publication (other academic/artistic)abstract The water-promoted elimination reactions of (R,S)-1-(1-X-ethyl)indene 1-X [X = Cl, Br, I, OBs (4-bromophenylsulfonyloxy)] and the corresponding (R,R) isomers 2-X in 25 vol% acetonitrile in water exhibit non-stereospecific and stereospecific 1,2 eliminati
11.	MENG, QS, et al. (author) SOLVENT-PROMOTED E2 REACTION COMPETING WITH S(N)2 REACTION AND STEPWISE SOLVOLYTIC ELIMINATION AND SUBSTITUTION-REACTIONS 1995 In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - : AMER CHEMICAL SOC. ; 117:37 Other publication (other academic/artistic)abstract Solvolysis of 9-(1-X-ethyl)fluorene (1-X, X = I, Br, Cl, OTs, or OBs) in 25 vol % acetonitrile in water gives the elimination products 9-(1-ethylidene)fluorene (3) and 9-vinylfluorene (2) and the substitution products 9-(1-hydroxyethyl)fluorene (1-OH) an
12.	Meng, QS, et al. (author) Stepwise and concerted solvolytic elimination and substitution reactions: E1 reaction via a primary carbocation 1997 In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - : AMER CHEMICAL SOC. ; 119:21 Other publication (other academic/artistic)abstract Solvolysis of 9-(X-methyl)fluorene (1-X, X = I, Br, OBs) in 25 vol % acetonitrile in water gives the elimination product 9-methylidenefluorene and the substitution products 9-(hydroxymethyl)fluorene (1-OH) and 9-(acetamidomethyl)fluorene (1-NHCOMe). Kine
13.	Meng, QS, et al. (author) The stereochemistry of solvent-promoted E1cB/E2 reactions of alpha-indenyl substituted ethyl halides 1996 In: CHEMICAL COMMUNICATIONS. - : ROYAL SOC CHEMISTRY. ; :3 Other publication (other academic/artistic)abstract The solvent-promoted elimination reactions of threo-1-(1-X-ethyl)indene 1-X (X = Cl, Br, I) and the corresponding erythro isomer 2-Br in 25 vol% acetonitrile in water at 55 degrees C, which are concluded to be of E1cB and E2 types, exhibit leaving-group
14.	Musliner, KL, et al. (author) Association of Polygenic Liabilities for Major Depression, Bipolar Disorder, and Schizophrenia With Risk for Depression in the Danish Population 2019 In: JAMA psychiatry. - Chicago : American Medical Association (AMA). - 2168-6238 .- 2168-622X. ; 76:5, s. 516-525 Journal article (peer-reviewed)
15.	Xie, Y, et al. (author) Genome of the Giant Panda Roundworm Illuminates Its Host Shift and Parasitic Adaptation 2022 In: Genomics, proteomics & bioinformatics. - : Elsevier BV. - 2210-3244 .- 1672-0229. ; 20:2, s. 366-381 Journal article (peer-reviewed)

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Type of publication: other publication (8); journal article (7)

Type of content: other academic/artistic (8); peer-reviewed (7)

Author/Editor: Chen, S. (4); Li, B. (4); Liu, Y. (4); Wang, F. (4); Wang, J. (4); Xu, L. (4); show more...; Yang, Y. (4); Zhang, H. (4); Zhang, L. (4); Zhao, L. (4); Li, J. (4); Kumar, S (4); Zhang, Y. (4); Martin, S. (4); Liu, Q. (4); Wang, D. (4); Wang, Z. (4); Wang, S (4); Ali, M (4); Singh, A (4); Chen, Z. (4); Zhou, J. (4); Yang, L. (4); Yang, J. (4); Sun, Y (4); Huang, S. (4); Harris, J. (4); Chen, Q. (4); Wu, J (4); Zhao, S (4); Rao, R (4); Gao, H. (4); Lee, C. (4); Bauer, M (4); Bernard, A (4); Zhang, XL (4); Chen, YJ (4); Huang, CS (4); Zhang, XY (4); Xia, ZY (4); Zhou, XJ (4); Zheng, L (4); Chen, YQ (4); Jin, L (4); Zhang, HY (4); Li, LW (4); Zheng, K (4); Kaushik, S (4); Lee, JM (4); Chen, LL (4); show less...

University: Uppsala University (9); Karolinska Institutet (6); Umeå University (2); Linköping University (2); Lund University (2); Stockholm University (1); show more...; Swedish University of Agricultural Sciences (1); show less...

Language: English (15)

Research subject (UKÄ/SCB): Medical and Health Sciences (5); Natural sciences (2)

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