首页 > 最新文献

Fieser and Fieser's Reagents for Organic Synthesis最新文献

英文 中文
Lanthanum nitrate 硝酸镧
Pub Date : 2019-10-03 DOI: 10.1002/9780471264194.fos06108.pub3
T. Ho, M. Fieser, L. Fieser
{"title":"Lanthanum nitrate","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.fos06108.pub3","DOIUrl":"https://doi.org/10.1002/9780471264194.fos06108.pub3","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82356864","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Phenyltrifluorosilane
Pub Date : 2019-10-03 DOI: 10.1002/9780471264194.fos08202.pub3
Tse‐Lok Ho, Mary Fieser, Louis Fieser
{"title":"Phenyltrifluorosilane","authors":"Tse‐Lok Ho, Mary Fieser, Louis Fieser","doi":"10.1002/9780471264194.fos08202.pub3","DOIUrl":"https://doi.org/10.1002/9780471264194.fos08202.pub3","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"32 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77789882","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tetrabutylammonium azide 四丁铵叠氮化
Pub Date : 2019-10-03 DOI: 10.1002/9780471264194.fos09485.pub3
T. Ho, M. Fieser, L. Fieser
{"title":"Tetrabutylammonium azide","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.fos09485.pub3","DOIUrl":"https://doi.org/10.1002/9780471264194.fos09485.pub3","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"30 1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83284283","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nitrosonium tetrafluoroborate
Pub Date : 2019-10-03 DOI: 10.1002/9780471264194.fos07452.pub3
T. Ho, M. Fieser, L. Fieser
{"title":"Nitrosonium tetrafluoroborate","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.fos07452.pub3","DOIUrl":"https://doi.org/10.1002/9780471264194.fos07452.pub3","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"62 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84279799","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Tetrabutylammonium cyanoborohydride 四丁铵cyanoborohydride
Pub Date : 2019-10-03 DOI: 10.1002/9780471264194.fos09494.pub3
T.-L. Ho, Mary Fieser, L. Fieser
{"title":"Tetrabutylammonium cyanoborohydride","authors":"T.-L. Ho, Mary Fieser, L. Fieser","doi":"10.1002/9780471264194.fos09494.pub3","DOIUrl":"https://doi.org/10.1002/9780471264194.fos09494.pub3","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"25 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77868774","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hexachlorodisilane
Pub Date : 2019-10-03 DOI: 10.1002/9780471264194.fos05499.pub3
Tse‐Lok Ho, Mary Fieser, Louis Fieser
{"title":"Hexachlorodisilane","authors":"Tse‐Lok Ho, Mary Fieser, Louis Fieser","doi":"10.1002/9780471264194.fos05499.pub3","DOIUrl":"https://doi.org/10.1002/9780471264194.fos05499.pub3","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"2015 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87236201","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acetylacetonato(dicarbonyl)rhodium( I ) 乙酰丙酮(二羰基)铑(I)
Pub Date : 2019-10-01 DOI: 10.1002/9780471264194.fos11688.pub7
Tse‐Lok Ho, Mary Fieser, Louis Fieser
{"title":"Acetylacetonato(dicarbonyl)rhodium(\u0000 I\u0000 )","authors":"Tse‐Lok Ho, Mary Fieser, Louis Fieser","doi":"10.1002/9780471264194.fos11688.pub7","DOIUrl":"https://doi.org/10.1002/9780471264194.fos11688.pub7","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77082366","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
( S )‐Proline Amides (S)‐脯氨酸酰胺
Pub Date : 2019-10-01 DOI: 10.1002/9780471264194.fos11524.pub5
T. Ho, M. Fieser, L. Fieser
{"title":"(\u0000 S\u0000 )‐Proline Amides","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.fos11524.pub5","DOIUrl":"https://doi.org/10.1002/9780471264194.fos11524.pub5","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"13 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85835355","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
( S )‐(2‐Pyrrolidinyl)azoles
Pub Date : 2019-10-01 DOI: 10.1002/9780471264194.fos11663.pub4
T. Ho, M. Fieser, L. Fieser
{"title":"(\u0000 \u0000 S\u0000 \u0000 )‐(2‐Pyrrolidinyl)azoles","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.fos11663.pub4","DOIUrl":"https://doi.org/10.1002/9780471264194.fos11663.pub4","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"12 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77180388","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bis(naphtho[2,1‐ c ])azepines
Pub Date : 2019-10-01 DOI: 10.1002/9780471264194.fos11589.pub5
T. Ho, M. Fieser, L. Fieser
{"title":"Bis(naphtho[2,1‐\u0000 c\u0000 ])azepines","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.fos11589.pub5","DOIUrl":"https://doi.org/10.1002/9780471264194.fos11589.pub5","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77243960","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Fieser and Fieser's Reagents for Organic Synthesis
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1