原创力文档- 1、原创力文档（book118）网站文档一经付费（服务费），不意味着购买了该文档的版权，仅供个人/单位学习、研究之用，不得用于商业用途，未经授权，严禁复制、发行、汇编、翻译或者网络传播等，侵权必究。。
- 2、本站所有内容均由合作方或网友上传，本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺！文档内容仅供研究参考，付费前请自行鉴别。如您付费，意味着您自己接受本站规则且自行承担风险，本站不退款、不进行额外附加服务；查看《如何避免下载的几个坑》。如果您已付费下载过本站文档，您可以点击 这里二次下载。
- 3、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等，请点击“版权申诉”（推荐），也可以打举报电话：400-050-0827(电话支持时间：9:00-18:30)。
- 4、该文档为VIP文档，如果想要下载，成为VIP会员后，下载免费。
- 5、成为VIP后，下载本文档将扣除1次下载权益。下载后，不支持退款、换文档。如有疑问请联系我们。
- 6、成为VIP后，您将拥有八大权益，权益包括：VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
- 7、VIP文档为合作方或网友上传，每下载1次， 网站将根据用户上传文档的质量评分、类型等，对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
Diels-Alder Reaction HeteroDiels-Alder Reaction Hetero Diels-Alder Reaction Stereochemistry Tetrahedron Lett. 1981, 4607. Diels-Alder Reaction HeteroDiels-Alder Reaction Miscellaneous Dienophiles C-N triple bond C-S double bond N-O double bond Diels-Alder Reaction HeteroDiels-Alder Reaction Miscellaneous Dienophiles N-S double bond S-S, S-O, Se-O double bond P-S double bond N-N triplele bond Diels-Alder Reaction HeteroDiels-Alder Reaction Hetero Diels-Alder Reaction-total synthesis Diels-Alder Reaction HeteroDiels-Alder Reaction Hetero Diels-Alder Reaction-total synthesis Diels-Alder Reaction Hetero Diels-Alder Reaction-total synthesis Diels-Alder Reaction Hetero Diels-Alder Reaction-total synthesis Diels-Alder Reaction Hetero Diels-Alder Reaction Suggested references Hetero Diels-Alder Methodology in Organic Synthesis, Boger, D.L. and Weinreb, S.N., Academic Press, 1987 Mechanistic Aspects of Diels-Alder Reactions: A Critical Survey, Sauer, Angew. Chem. Int. Ed., 1980, 19, 779-807 DA Reactions Part II: The Reaction Mechanism, Sauer, Angew. Chem. Int. Ed., 1967, 6, 16-33 DA Reactions Part I: New Preparative Aspects, Sauer, Angew. Chem. Int. Ed., 1966, 5, 211-230 Synthetic Aspects of D-A Cycloadditions with Heterodienophiles, Weinreb, Tetrahedron, 1982, 38, 3087-3128 [2+2] cycloaddition [2+2] cycloaddition Reaction [2+2] cycloaddition Reaction [2+2] cycloaddition [2+2] cycloaddition Reaction---cases [2+2] cycloaddition-Reaction types F2C=CX2(X=F, Cl) especially F2C=CF2 form cyclobutanes with many alkenes. ([2+2] preferred with conjugated diene) Allenes and ketenes react with activated olefins and alkyne to form cyclobutanes. ([2+2] preferred with conjugated diene for ketenes) Benzynes undergoes [2+2] with certain olefins Enamides formation from Michael-type olefins and ketenes [2+2] cycloaddition Reaction---cases Sch?fer, Angew. Chem. 1967, 79, 54. Dauben, Tet. 1961, 15, 197. [2+2] cycloaddition Reaction---cases Sch?fer, Angew. Chem. 1967, 79, 54. Dauben, Tet. 1
文档评论（0）