Design, synthesis and evaluation of novel cis-p-menthane type Schiff base compounds as effective herbicides
p-Menthane type monoterpene derivatives were identified as bio-based compounds with high herbicidal activities. In order to search novel p-menthane type monoterpene derivatives in good performance, a series of novel cis-p-menthane type Schiff base derivatives were designed and synthesized. All targe...
Saved in:
Published in | Chinese chemical letters Vol. 28; no. 7; pp. 1509 - 1513 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.07.2017
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | p-Menthane type monoterpene derivatives were identified as bio-based compounds with high herbicidal activities. In order to search novel p-menthane type monoterpene derivatives in good performance, a series of novel cis-p-menthane type Schiff base derivatives were designed and synthesized. All target products were easily available novel compounds and characterized by FT-IR,^1H NMR,^13 C NMR and ESI+-MS. Their pre-emergence herbicidal activities against annual ryegrass were evaluated. The bioassays indicated that most of the target compounds displayed excellent herbicidal activities in pre-emergence treatment. |
---|---|
AbstractList | [Display omitted]
A series of cis-p-menthane type Schiff base derivatives were designed and synthesized as novel herbicides. Most target compounds displayed excellent herbicidal activities against annual ryegrass in pre-emergence treatment.
p-Menthane type monoterpene derivatives were identified as bio-based compounds with high herbicidal activities. In order to search novel p-menthane type monoterpene derivatives in good performance, a series of novel cis-p-menthane type Schiff base derivatives were designed and synthesized. All target products were easily available novel compounds and characterized by FT-IR, 1H NMR, 13C NMR and ESI+-MS. Their pre-emergence herbicidal activities against annual ryegrass were evaluated. The bioassays indicated that most of the target compounds displayed excellent herbicidal activities in pre-emergence treatment. p-Menthane type monoterpene derivatives were identified as bio-based compounds with high herbicidal activities. In order to search novel p-menthane type monoterpene derivatives in good performance, a series of novel cis-p-menthane type Schiff base derivatives were designed and synthesized. All target products were easily available novel compounds and characterized by FT-IR,^1H NMR,^13 C NMR and ESI+-MS. Their pre-emergence herbicidal activities against annual ryegrass were evaluated. The bioassays indicated that most of the target compounds displayed excellent herbicidal activities in pre-emergence treatment. |
Author | Shi-Chao Xu Shou-Ji Zhu Jing Wang Liang-Wu Bi Yu-Xiang Chen Yan-Ju Lu Yan Gu Zhen-Dong Zhao |
AuthorAffiliation | Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing 210042, China Key Lab, of Bioraass Energy and Material, fiangsu Province, Nanjing 210042, China National Engineering Lab. for Biomass Chemical Utilization, Nanjing 210042, China Key and Open Lab. on Forest Chemical Engineering, State Forestry Administration, Nanjing 210042, China Institute of Forestry New Technology, Chinese Academy of Forestry, Beijing 100091, China 2011 Collaborative Innovation Center of fiangxi Typical Trees Cultivation and Utilization in flangxi Agricultural University, Nanchang 33,0045, China |
Author_xml | – sequence: 1 givenname: Shi-Chao surname: Xu fullname: Xu, Shi-Chao organization: Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing 210042, China – sequence: 2 givenname: Shou-Ji surname: Zhu fullname: Zhu, Shou-Ji organization: Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing 210042, China – sequence: 3 givenname: Jing surname: Wang fullname: Wang, Jing organization: Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing 210042, China – sequence: 4 givenname: Liang-Wu surname: Bi fullname: Bi, Liang-Wu organization: Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing 210042, China – sequence: 5 givenname: Yu-Xiang surname: Chen fullname: Chen, Yu-Xiang organization: Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing 210042, China – sequence: 6 givenname: Yan-Ju surname: Lu fullname: Lu, Yan-Ju organization: Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing 210042, China – sequence: 7 givenname: Yan surname: Gu fullname: Gu, Yan organization: Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing 210042, China – sequence: 8 givenname: Zhen-Dong surname: Zhao fullname: Zhao, Zhen-Dong email: zdzhao@189.cn organization: Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing 210042, China |
BookMark | eNqFkLlOAzEQQC0EEuH4AhqLml3seNe7LigQtxSJgvSWj3HisLHDeomUv8c5REFDNSPNvDneGToOMQBCV5SUlFB-uyiN6WAox4Q2JWElIfURGtG2aYta8Oo454TQoq1oc4rOUloQMm5bxkfo8xGSn4UbnDZhmOc8YRUshrXqvtXgY8DR4RDX0GHjU7EqlpD7VAA8bFaAP8zcO4e1SoBNXK7id7B5QsLgHJjBrwHPodfeeAvpAp041SW4PMRzNH1-mj68FpP3l7eH-0lhGCNDoanWllLFK9Dc2britlLMippqoaimhlBlqlaA0JZbBaxxucIVCMGqcc3OEduPNX1MqQcnV71fqn4jKZFbXXIhd7rkVpckTGZdmRJ_KOOHnYGhV777h73bs5C_WnvoZTIeggHr-2xB2uj_4a8Pu-cxzL58mP2ezJuxqDghjP0A63yXcg |
CitedBy_id | crossref_primary_10_1039_D1RA04910K crossref_primary_10_1021_acs_jafc_9b05441 crossref_primary_10_1002_slct_202200618 crossref_primary_10_1002_cbdv_202100746 crossref_primary_10_1021_acs_jafc_0c01909 crossref_primary_10_1039_D2CS00509C crossref_primary_10_1016_j_indcrop_2024_118833 crossref_primary_10_1039_D0NJ00583E crossref_primary_10_1016_j_cej_2022_134582 crossref_primary_10_1021_acs_jafc_2c00635 crossref_primary_10_1002_cbdv_202301867 crossref_primary_10_1002_ps_8323 |
Cites_doi | 10.1002/ps.2780210207 10.1016/j.cclet.2016.06.019 10.1016/j.algal.2013.08.001 10.1016/j.cclet.2008.04.009 10.1021/jf051928j 10.1039/C3OB41971A 10.1021/jf051494s 10.1016/j.cclet.2014.03.046 10.1002/ps.3339 10.1016/j.cclet.2015.03.026 10.1016/S0261-2194(00)00076-4 10.1017/S0043174500093474 10.1021/jf902035w 10.1111/j.1744-7348.2005.04018.x 10.1016/j.fct.2013.01.033 10.1016/j.bmcl.2015.10.064 10.1016/j.bmc.2015.08.037 10.1021/acs.jafc.6b03977 10.1016/j.cclet.2015.04.008 10.1016/S0269-7491(00)00110-X 10.1007/BF00598074 10.1016/j.microc.2012.07.003 10.1016/j.indcrop.2015.10.032 10.1016/j.tetlet.2012.11.081 10.1021/acssuschemeng.6b00819 10.1002/anie.201202354 |
ContentType | Journal Article |
Copyright | 2017 |
Copyright_xml | – notice: 2017 |
DBID | 2RA 92L CQIGP ~WA AAYXX CITATION |
DOI | 10.1016/j.cclet.2017.03.005 |
DatabaseName | 维普期刊资源整合服务平台 中文科技期刊数据库-CALIS站点 中文科技期刊数据库-7.0平台 中文科技期刊数据库- 镜像站点 CrossRef |
DatabaseTitle | CrossRef |
DatabaseTitleList | |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry |
DocumentTitleAlternate | Design, synthesis and evaluation of novel cis-p-menthane type Schiff base compounds as effective herbicides |
EISSN | 1878-5964 |
EndPage | 1513 |
ExternalDocumentID | 10_1016_j_cclet_2017_03_005 S1001841717300839 672946003 |
GroupedDBID | --K --M .~1 0R~ 188 1B1 1~. 1~5 29B 2B. 2C. 2RA 2WC 4.4 457 4G. 5GY 5VR 5VS 6J9 7-5 71M 8P~ 8RM 92E 92I 92L 92Q 93N AABNK AACTN AAEDT AAEDW AAIAV AAIKJ AAKOC AALRI AAOAW AAQFI AARLI AAXUO ABFNM ABFRF ABJNI ABMAC ABXDB ABYKQ ACDAQ ACGFO ACGFS ACNNM ACRLP ADBBV ADECG ADEZE ADMUD AEBSH AEFWE AEKER AENEX AFKWA AFTJW AFUIB AFZHZ AGHFR AGUBO AGYEJ AIEXJ AIKHN AITUG AJBFU AJOXV AJSZI ALMA_UNASSIGNED_HOLDINGS AMFUW AMRAJ AXJTR BKOJK BLXMC C1A CCEZO CDRFL CHBEP CQIGP CS3 CW9 DU5 EBS EFJIC EFLBG EJD EO9 EP2 EP3 F5P FA0 FDB FEDTE FIRID FLBIZ FNPLU FYGXN GBLVA GX1 HVGLF HZ~ J1W KOM M41 MO0 N9A O-L O9- OAUVE OK1 OZT P-8 P-9 P2P PC. Q38 RIG ROL RPZ S.. SDF SDG SDH SES SPC SPCBC SSK SSZ T5K TCJ TGP UNMZH UZ4 ~G- ~WA -SB -S~ 5XA 5XC AATTM AAXKI AAYWO AAYXX ABWVN ACRPL ACVFH ADCNI ADNMO AEIPS AEUPX AFPUW AFXIZ AGCQF AGRNS AIGII AIIUN AKBMS AKRWK AKYEP ANKPU APXCP BNPGV CAJEB CITATION Q-- SSH U1G U5L |
ID | FETCH-LOGICAL-c330t-b1bbd11a64eb6fd546d4a3d951b9a1b1c01ac489e9bd6dae37f1b96ae9934253 |
IEDL.DBID | .~1 |
ISSN | 1001-8417 |
IngestDate | Thu Apr 24 22:54:57 EDT 2025 Tue Jul 01 03:18:50 EDT 2025 Fri Feb 23 02:32:35 EST 2024 Wed Feb 14 09:58:29 EST 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 7 |
Keywords | Turpentine derivatives Bio-based herbicides Herbicidal activity Schiff base derivatives p-Menthane type compounds |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c330t-b1bbd11a64eb6fd546d4a3d951b9a1b1c01ac489e9bd6dae37f1b96ae9934253 |
Notes | Turpentine derivatives Bio-based herbicides p-Menthane type compounds Schiff base derivatives Herbicidal activity p-Menthane type monoterpene derivatives were identified as bio-based compounds with high herbicidal activities. In order to search novel p-menthane type monoterpene derivatives in good performance, a series of novel cis-p-menthane type Schiff base derivatives were designed and synthesized. All target products were easily available novel compounds and characterized by FT-IR,^1H NMR,^13 C NMR and ESI+-MS. Their pre-emergence herbicidal activities against annual ryegrass were evaluated. The bioassays indicated that most of the target compounds displayed excellent herbicidal activities in pre-emergence treatment. 11-2710/O6 |
PageCount | 5 |
ParticipantIDs | crossref_primary_10_1016_j_cclet_2017_03_005 crossref_citationtrail_10_1016_j_cclet_2017_03_005 elsevier_sciencedirect_doi_10_1016_j_cclet_2017_03_005 chongqing_primary_672946003 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2017-07-01 |
PublicationDateYYYYMMDD | 2017-07-01 |
PublicationDate_xml | – month: 07 year: 2017 text: 2017-07-01 day: 01 |
PublicationDecade | 2010 |
PublicationTitle | Chinese chemical letters |
PublicationTitleAlternate | Chinese Chemical Letters |
PublicationYear | 2017 |
Publisher | Elsevier B.V |
Publisher_xml | – name: Elsevier B.V |
References | Li, Qian, Cui (bib0005) 2006; 54 Zheng, Wu, Guo (bib0015) 2015; 26 Huang, Li, Liu, Wei (bib0065) 2014; 4 Grayson, Williams, Freehauf, Pease, Ziesel, Sereno, Reinsfelder (bib0080) 1987; 21 Hanazato (bib0030) 2001; 112 Duke, Romagni, Dayan (bib0055) 2000; 19 Aggarwal, Kumar, Dureja, Rawat (bib0100) 2009; 57 Liu, Zhai, Xu (bib0050) 2015; 25 Wang, Li, Wang, Ma, Li (bib0060) 2008; 19 Zhu, Xu, Wang, Zhao, Jiang (bib0110) 2016; 64 Baalouch, De Mesmaeker, Beaudegnies (bib0020) 2013; 54 Yue, Li, Liu (bib0045) 2014; 25 Tang, Feng (bib0135) 2002 Vaughn, Spencer (bib0085) 1996; 44 Li, Li, Gao (bib0090) 2016; 4 Singh, Batish, Setia, Kohli (bib0035) 2005; 146 Kovals'skaya, Kozlov, Tikhonova (bib0120) 1989; 25 Samadhiya, Havle (bib0095) 2001; 17 Xie, Chi, Guan (bib0025) 2016; 24 Shimizu, Morimoto, Zhang, Ohshima (bib0125) 2012; 51 Huo, Ma, Zhang (bib0010) 2016; 27 Huang, Huang, Ren (bib0140) 2005; 53 Gao, Li, Chen (bib0070) 2015; 78 Hernández-Moreno, Soffers, Wiratno (bib0040) 2013; 56 Guo, Li, Ma (bib0115) 2015; 26 Sultane, Mete, Bhat (bib0130) 2014; 12 Zhang, Xu, Cui, Xie, Kong (bib0075) 2012; 68 Sandín-España, Sevilla-Morán, Calvo, Mateo-Miranda, Alonso-Prados (bib0105) 2013; 106 Yue (10.1016/j.cclet.2017.03.005_bib0045) 2014; 25 Samadhiya (10.1016/j.cclet.2017.03.005_bib0095) 2001; 17 Liu (10.1016/j.cclet.2017.03.005_bib0050) 2015; 25 Li (10.1016/j.cclet.2017.03.005_bib0005) 2006; 54 Li (10.1016/j.cclet.2017.03.005_bib0090) 2016; 4 Xie (10.1016/j.cclet.2017.03.005_bib0025) 2016; 24 Gao (10.1016/j.cclet.2017.03.005_bib0070) 2015; 78 Zheng (10.1016/j.cclet.2017.03.005_bib0015) 2015; 26 Zhu (10.1016/j.cclet.2017.03.005_bib0110) 2016; 64 Huo (10.1016/j.cclet.2017.03.005_bib0010) 2016; 27 Sultane (10.1016/j.cclet.2017.03.005_bib0130) 2014; 12 Huang (10.1016/j.cclet.2017.03.005_bib0065) 2014; 4 Hernández-Moreno (10.1016/j.cclet.2017.03.005_bib0040) 2013; 56 Aggarwal (10.1016/j.cclet.2017.03.005_bib0100) 2009; 57 Sandín-España (10.1016/j.cclet.2017.03.005_bib0105) 2013; 106 Vaughn (10.1016/j.cclet.2017.03.005_bib0085) 1996; 44 Grayson (10.1016/j.cclet.2017.03.005_bib0080) 1987; 21 Hanazato (10.1016/j.cclet.2017.03.005_bib0030) 2001; 112 Huang (10.1016/j.cclet.2017.03.005_bib0140) 2005; 53 Wang (10.1016/j.cclet.2017.03.005_bib0060) 2008; 19 Guo (10.1016/j.cclet.2017.03.005_bib0115) 2015; 26 Zhang (10.1016/j.cclet.2017.03.005_bib0075) 2012; 68 Baalouch (10.1016/j.cclet.2017.03.005_bib0020) 2013; 54 Singh (10.1016/j.cclet.2017.03.005_bib0035) 2005; 146 Shimizu (10.1016/j.cclet.2017.03.005_bib0125) 2012; 51 Duke (10.1016/j.cclet.2017.03.005_bib0055) 2000; 19 Tang (10.1016/j.cclet.2017.03.005_bib0135) 2002 Kovals'skaya (10.1016/j.cclet.2017.03.005_bib0120) 1989; 25 |
References_xml | – volume: 51 start-page: 8564 year: 2012 end-page: 8567 ident: bib0125 article-title: Microwave-assisted deacylation of unactivated amides using ammonium-salt-accelerated transamidation publication-title: Angew. Chem. Int. Ed. – volume: 19 start-page: 651 year: 2008 end-page: 654 ident: bib0060 article-title: Molecular design, synthesis and biological activities of amidines as new ketol-acid reductoisomerase inhibitors publication-title: Chin. Chem. Lett. – volume: 26 start-page: 1008 year: 2015 end-page: 1010 ident: bib0015 article-title: Design, synthesis and herbicidal activities of novel self-dispreading phenoxy carboxylic acid derivatives for the control of water hyacinth floating on the water surface publication-title: Chin. Chem. Lett. – volume: 4 start-page: 4685 year: 2016 end-page: 4691 ident: bib0090 article-title: Taking advantage of a sustainable forest resource in agriculture: A value-added application of volatile turpentine analogues as botanical pesticides based on amphipathic modification and QSAR study publication-title: ACS Sustain. Chem. Eng. – volume: 25 start-page: 5524 year: 2015 end-page: 5528 ident: bib0050 article-title: Facile and efficient synthesis and herbicidal activity determination of novel 1,2,4-triazolo[4,3-α]pyridin-3(2H)-one derivatives via microwave irradiation publication-title: Bioorg. Med. Chem. Lett. – volume: 53 start-page: 7908 year: 2005 end-page: 7914 ident: bib0140 article-title: Synthesis and herbicidal activity of 2-(7-fluoro-3-oxo-3,4-dihydro-2H-benzo[b][1,4] oxazin-6-yl)isoindoline-1,3-diones publication-title: J. Agric. Food Chem. – volume: 146 start-page: 89 year: 2005 end-page: 94 ident: bib0035 article-title: Herbicidal activity of volatile oils from publication-title: Ann. Appl. Biol. – volume: 68 start-page: 1512 year: 2012 end-page: 1522 ident: bib0075 article-title: Synthesis and herbicidal potential of substituted aurones publication-title: Pest Manag. Sci. – volume: 21 start-page: 143 year: 1987 end-page: 153 ident: bib0080 article-title: The physical and chemical properties of the herbicide cinmethylin (SD 95481) publication-title: Pest Manag. Sci. – volume: 44 start-page: 7 year: 1996 end-page: 11 ident: bib0085 article-title: Synthesis and herbicidal activity of modified monoterpenes structurally similar to cinmethylin publication-title: Weed Sci. – volume: 4 start-page: 62 year: 2014 end-page: 69 ident: bib0065 article-title: Botanical pesticides as potential rotifer-control agents in microalgal mass culture publication-title: Algal Res. – volume: 64 start-page: 9702 year: 2016 end-page: 9707 ident: bib0110 article-title: Synthesis and herbicidal activities of publication-title: J. Agric. Food Chem. – volume: 25 start-page: 552 year: 1989 end-page: 557 ident: bib0120 article-title: Stereoselective synthesis of N,N’-diacyl-p-menthane-1,8-diamines publication-title: Chem. Nat. Compd. – volume: 54 start-page: 125 year: 2006 end-page: 129 ident: bib0005 article-title: Synthesis and herbicidal activity of novel 3-aminocarbonyl-2-oxazolidinethione derivatives containing a substituted pyridine ring publication-title: J. Agric. Food Chem. – volume: 19 start-page: 583 year: 2000 end-page: 589 ident: bib0055 article-title: Natural products as sources for new mechanisms of herbicidal action publication-title: Crop Protect. – volume: 17 start-page: 119 year: 2001 end-page: 122 ident: bib0095 article-title: Synthetic utility of Schiff bases as potential herbicidal agents publication-title: Orient. J. Chem. – volume: 27 start-page: 1547 year: 2016 end-page: 1550 ident: bib0010 article-title: Synthesis and biological activity of novel N-(3-furan-2-yl-1-phenyl-1H-pyrazol-5-yl) amides derivatives publication-title: Chin. Chem. Lett. – volume: 112 start-page: 1 year: 2001 end-page: 10 ident: bib0030 article-title: Pesticide effects on freshwater zooplankton: an ecological perspective publication-title: Environ. Pollut. – volume: 56 start-page: 483 year: 2013 end-page: 490 ident: bib0040 article-title: Consumer and farmer safety evaluation of application of botanical pesticides in black pepper crop protection publication-title: Food Chem. Toxicol. – volume: 25 start-page: 1069 year: 2014 end-page: 1072 ident: bib0045 article-title: N-Fluorinated phenyl-N’-pyrimidyl urea derivatives: Synthesis, biological evaluation and 3D-QSAR study publication-title: Chin. Chem. Lett. – year: 2002 ident: bib0135 article-title: DPS Data Processing System for Practical Statistics – volume: 12 start-page: 261 year: 2014 end-page: 264 ident: bib0130 article-title: Chemoselective N-deacetylation under mild conditions publication-title: Org. Biomol. Chem. – volume: 78 start-page: 131 year: 2015 end-page: 140 ident: bib0070 article-title: High value-added application of rosin as a potential renewable source for the synthesis of acrylopimaric acid-based botanical herbicides publication-title: Ind. Crops Prod. – volume: 24 start-page: 428 year: 2016 end-page: 434 ident: bib0025 article-title: Synthesis and evaluation of substituted 3-(pyridin-2-yl) benzenesulfonamide derivatives as potent herbicidal agents publication-title: Bioorg. Med. Chem. – volume: 26 start-page: 755 year: 2015 end-page: 758 ident: bib0115 article-title: Synthesis and antitumor activity of publication-title: Chin. Chem. Lett. – volume: 54 start-page: 557 year: 2013 end-page: 561 ident: bib0020 article-title: Efficient synthesis of bicyclo[3.2.1]octane-2,4-diones and their incorporation into potent HPPD inhibitors publication-title: Tetrahedron Lett. – volume: 106 start-page: 212 year: 2013 end-page: 219 ident: bib0105 article-title: Photochemical behavior of alloxydim herbicide in environmental waters. Structural elucidation and toxicity of degradation products publication-title: Microchem. J. – volume: 57 start-page: 8520 year: 2009 end-page: 8525 ident: bib0100 article-title: Schiff bases as potential fungicides and nitrification inhibitors publication-title: J. Agric. Food Chem. – volume: 21 start-page: 143 year: 1987 ident: 10.1016/j.cclet.2017.03.005_bib0080 article-title: The physical and chemical properties of the herbicide cinmethylin (SD 95481) publication-title: Pest Manag. Sci. doi: 10.1002/ps.2780210207 – volume: 27 start-page: 1547 year: 2016 ident: 10.1016/j.cclet.2017.03.005_bib0010 article-title: Synthesis and biological activity of novel N-(3-furan-2-yl-1-phenyl-1H-pyrazol-5-yl) amides derivatives publication-title: Chin. Chem. Lett. doi: 10.1016/j.cclet.2016.06.019 – year: 2002 ident: 10.1016/j.cclet.2017.03.005_bib0135 – volume: 4 start-page: 62 year: 2014 ident: 10.1016/j.cclet.2017.03.005_bib0065 article-title: Botanical pesticides as potential rotifer-control agents in microalgal mass culture publication-title: Algal Res. doi: 10.1016/j.algal.2013.08.001 – volume: 19 start-page: 651 year: 2008 ident: 10.1016/j.cclet.2017.03.005_bib0060 article-title: Molecular design, synthesis and biological activities of amidines as new ketol-acid reductoisomerase inhibitors publication-title: Chin. Chem. Lett. doi: 10.1016/j.cclet.2008.04.009 – volume: 54 start-page: 125 year: 2006 ident: 10.1016/j.cclet.2017.03.005_bib0005 article-title: Synthesis and herbicidal activity of novel 3-aminocarbonyl-2-oxazolidinethione derivatives containing a substituted pyridine ring publication-title: J. Agric. Food Chem. doi: 10.1021/jf051928j – volume: 17 start-page: 119 year: 2001 ident: 10.1016/j.cclet.2017.03.005_bib0095 article-title: Synthetic utility of Schiff bases as potential herbicidal agents publication-title: Orient. J. Chem. – volume: 12 start-page: 261 year: 2014 ident: 10.1016/j.cclet.2017.03.005_bib0130 article-title: Chemoselective N-deacetylation under mild conditions publication-title: Org. Biomol. Chem. doi: 10.1039/C3OB41971A – volume: 53 start-page: 7908 year: 2005 ident: 10.1016/j.cclet.2017.03.005_bib0140 article-title: Synthesis and herbicidal activity of 2-(7-fluoro-3-oxo-3,4-dihydro-2H-benzo[b][1,4] oxazin-6-yl)isoindoline-1,3-diones publication-title: J. Agric. Food Chem. doi: 10.1021/jf051494s – volume: 25 start-page: 1069 year: 2014 ident: 10.1016/j.cclet.2017.03.005_bib0045 article-title: N-Fluorinated phenyl-N’-pyrimidyl urea derivatives: Synthesis, biological evaluation and 3D-QSAR study publication-title: Chin. Chem. Lett. doi: 10.1016/j.cclet.2014.03.046 – volume: 68 start-page: 1512 year: 2012 ident: 10.1016/j.cclet.2017.03.005_bib0075 article-title: Synthesis and herbicidal potential of substituted aurones publication-title: Pest Manag. Sci. doi: 10.1002/ps.3339 – volume: 26 start-page: 755 year: 2015 ident: 10.1016/j.cclet.2017.03.005_bib0115 article-title: Synthesis and antitumor activity of a-aminophosphonate derivatives containing thieno[2,3-d]pyrimidines publication-title: Chin. Chem. Lett. doi: 10.1016/j.cclet.2015.03.026 – volume: 19 start-page: 583 year: 2000 ident: 10.1016/j.cclet.2017.03.005_bib0055 article-title: Natural products as sources for new mechanisms of herbicidal action publication-title: Crop Protect. doi: 10.1016/S0261-2194(00)00076-4 – volume: 44 start-page: 7 year: 1996 ident: 10.1016/j.cclet.2017.03.005_bib0085 article-title: Synthesis and herbicidal activity of modified monoterpenes structurally similar to cinmethylin publication-title: Weed Sci. doi: 10.1017/S0043174500093474 – volume: 57 start-page: 8520 year: 2009 ident: 10.1016/j.cclet.2017.03.005_bib0100 article-title: Schiff bases as potential fungicides and nitrification inhibitors publication-title: J. Agric. Food Chem. doi: 10.1021/jf902035w – volume: 146 start-page: 89 year: 2005 ident: 10.1016/j.cclet.2017.03.005_bib0035 article-title: Herbicidal activity of volatile oils from Eucalyptus citriodora against Parthenium hysterophorus publication-title: Ann. Appl. Biol. doi: 10.1111/j.1744-7348.2005.04018.x – volume: 56 start-page: 483 year: 2013 ident: 10.1016/j.cclet.2017.03.005_bib0040 article-title: Consumer and farmer safety evaluation of application of botanical pesticides in black pepper crop protection publication-title: Food Chem. Toxicol. doi: 10.1016/j.fct.2013.01.033 – volume: 25 start-page: 5524 year: 2015 ident: 10.1016/j.cclet.2017.03.005_bib0050 article-title: Facile and efficient synthesis and herbicidal activity determination of novel 1,2,4-triazolo[4,3-α]pyridin-3(2H)-one derivatives via microwave irradiation publication-title: Bioorg. Med. Chem. Lett. doi: 10.1016/j.bmcl.2015.10.064 – volume: 24 start-page: 428 year: 2016 ident: 10.1016/j.cclet.2017.03.005_bib0025 article-title: Synthesis and evaluation of substituted 3-(pyridin-2-yl) benzenesulfonamide derivatives as potent herbicidal agents publication-title: Bioorg. Med. Chem. doi: 10.1016/j.bmc.2015.08.037 – volume: 64 start-page: 9702 year: 2016 ident: 10.1016/j.cclet.2017.03.005_bib0110 article-title: Synthesis and herbicidal activities of p-menth-3-en-1-amine and its schiff base derivatives publication-title: J. Agric. Food Chem. doi: 10.1021/acs.jafc.6b03977 – volume: 26 start-page: 1008 year: 2015 ident: 10.1016/j.cclet.2017.03.005_bib0015 article-title: Design, synthesis and herbicidal activities of novel self-dispreading phenoxy carboxylic acid derivatives for the control of water hyacinth floating on the water surface publication-title: Chin. Chem. Lett. doi: 10.1016/j.cclet.2015.04.008 – volume: 112 start-page: 1 year: 2001 ident: 10.1016/j.cclet.2017.03.005_bib0030 article-title: Pesticide effects on freshwater zooplankton: an ecological perspective publication-title: Environ. Pollut. doi: 10.1016/S0269-7491(00)00110-X – volume: 25 start-page: 552 year: 1989 ident: 10.1016/j.cclet.2017.03.005_bib0120 article-title: Stereoselective synthesis of N,N’-diacyl-p-menthane-1,8-diamines publication-title: Chem. Nat. Compd. doi: 10.1007/BF00598074 – volume: 106 start-page: 212 year: 2013 ident: 10.1016/j.cclet.2017.03.005_bib0105 article-title: Photochemical behavior of alloxydim herbicide in environmental waters. Structural elucidation and toxicity of degradation products publication-title: Microchem. J. doi: 10.1016/j.microc.2012.07.003 – volume: 78 start-page: 131 year: 2015 ident: 10.1016/j.cclet.2017.03.005_bib0070 article-title: High value-added application of rosin as a potential renewable source for the synthesis of acrylopimaric acid-based botanical herbicides publication-title: Ind. Crops Prod. doi: 10.1016/j.indcrop.2015.10.032 – volume: 54 start-page: 557 year: 2013 ident: 10.1016/j.cclet.2017.03.005_bib0020 article-title: Efficient synthesis of bicyclo[3.2.1]octane-2,4-diones and their incorporation into potent HPPD inhibitors publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2012.11.081 – volume: 4 start-page: 4685 year: 2016 ident: 10.1016/j.cclet.2017.03.005_bib0090 article-title: Taking advantage of a sustainable forest resource in agriculture: A value-added application of volatile turpentine analogues as botanical pesticides based on amphipathic modification and QSAR study publication-title: ACS Sustain. Chem. Eng. doi: 10.1021/acssuschemeng.6b00819 – volume: 51 start-page: 8564 year: 2012 ident: 10.1016/j.cclet.2017.03.005_bib0125 article-title: Microwave-assisted deacylation of unactivated amides using ammonium-salt-accelerated transamidation publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.201202354 |
SSID | ssj0028836 |
Score | 2.175371 |
Snippet | p-Menthane type monoterpene derivatives were identified as bio-based compounds with high herbicidal activities. In order to search novel p-menthane type... [Display omitted] A series of cis-p-menthane type Schiff base derivatives were designed and synthesized as novel herbicides. Most target compounds displayed... |
SourceID | crossref elsevier chongqing |
SourceType | Enrichment Source Index Database Publisher |
StartPage | 1509 |
SubjectTerms | Bio-based herbicides Herbicidal activity ne型 p-Menthane type compounds Schiff base derivatives Turpentine derivatives 化合物 合成 希夫碱 设计 评价 除草剂 除草活性 |
Title | Design, synthesis and evaluation of novel cis-p-menthane type Schiff base compounds as effective herbicides |
URI | http://lib.cqvip.com/qk/84039X/201707/672946003.html https://dx.doi.org/10.1016/j.cclet.2017.03.005 |
Volume | 28 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV07T8MwELYQDLAgnqI8Kg-MmNa14zYjKlQFBAsgsVl-hQaqtJCCxMJv5y6PAhJiYMzDVnTn3H1xvvuOkMPQtd4bzlnkYsVkzA0z0lsGqVf4JPaeO6x3vrpWwzt5cR_dL5B-XQuDtMoq9pcxvYjW1ZlWZc3WNE1bN6ge1JMcfyMjkMAiPim7uMqPP-Y0D2ymW1QYIXUI766VhwqOl4PJkFDJu6XSaYQKC6NJ9vAMeeP3TPUt-wzWyGoFG-lJ-WTrZCFkG2S5X3dr2yRPpwUV44jm7xlgujzNqck8_RLzppOEZpO3MKYuzdmU4a7gyGSB4iYsvXGjNEko5jSKLHNstgQz5LTke0BIpOBcm7rUh3yL3A7ObvtDVjVSYE6I9oxZbq3n3CgZrEp8JJWXRngAVzY23HLX5sbJXhxi65U3QXQTuKJMAPAC77TYJovZJAs7hHaEiqQzXAYTSWvBuBy-xttJL3Q6LkjbIHtz--lpqZehFQB4CcBKNEintqh2lQQ5dsIY65pr9qgLl2h0iW4LDS5pkKP5oHrGP29Xtav0j4WkIUf8NXD3vwP3yAoelRzefbI4e3kNB4BUZrZZLMUmWTo5vxxefwJDNuot |
linkProvider | Elsevier |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LTxsxEB7RcKCXqqWtmlKKDxyxEsdeZ_eIAii8ciGVuFl-bbMt2gQ2rdR_35l9BCpVHLiuPdbK45357P38DcBhHLsQrBA88ZnmKhOWWxUcx9QrQ56FIDzdd76e6ek3dXGb3G7BpLsLQ7TKNvY3Mb2O1u2TQTubg1VRDG5IPShVgn4jE5DIXsE2qVMlPdg-Pr-czjb7rjStKwVSf04GnfhQTfPyOB5xKsW4ETtNSGRhsSy_32Pq-H-yepKAzt7CmxY5suPm5d7BVix3YWfSFWx7Dz9PajbGEav-lAjrqqJitgzsUc-bLXNWLn_HO-aLiq84HQwubBkZncOyG78o8pxRWmNENKd6SzhCxRrKB0ZFhv51hS9CrD7A_Ox0PpnytpYC91IO19wJ54IQVqvodB4SpYOyMiC-cpkVTvihsF6lWcxc0MFGOc6xRduI-AU_a_kReuWyjJ-AjaROlLdCRZso53ByBW7Ih3kaRyMflevD3mb-zKqRzDAaMbxCbCX7MOpm1PhWhZyKYdyZjm72w9QuMeQSM5QGXdKHo41RN-Kz3XXnKvPPWjKYJp4z_PxSwwPYmc6vr8zV-exyD15TS0Pp_QK99cOvuI_AZe2-tgvzL0vH7N4 |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Design%2C+synthesis+and+evaluation+of+novel+cis-p-menthane+type+Schiff+base+compounds+as+effective+herbicides&rft.jtitle=Chinese+chemical+letters&rft.au=Xu%2C+Shi-Chao&rft.au=Zhu%2C+Shou-Ji&rft.au=Wang%2C+Jing&rft.au=Bi%2C+Liang-Wu&rft.date=2017-07-01&rft.pub=Elsevier+B.V&rft.issn=1001-8417&rft.eissn=1878-5964&rft.volume=28&rft.issue=7&rft.spage=1509&rft.epage=1513&rft_id=info:doi/10.1016%2Fj.cclet.2017.03.005&rft.externalDocID=S1001841717300839 |
thumbnail_s | http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=http%3A%2F%2Fimage.cqvip.com%2Fvip1000%2Fqk%2F84039X%2F84039X.jpg |