PhanePhos and Related Derivatives

L. A. Adrio, K. K. Hii
{"title":"PhanePhos and Related Derivatives","authors":"L. A. Adrio, K. K. Hii","doi":"10.1002/047084289X.RN01475","DOIUrl":null,"url":null,"abstract":"(R)-4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane [364732-88-7] C40H34P2 (MW 576.65) \n \nInChI = 1S/C40H34P2/c1-5-13-35(14-6-1)41(36-15-7-2-8-16-36)39-29-31-21-25-33(39)27-23-32-22-26-34(28-24-31)40(30-32)42(37-17-9-3-10-18-37)38-19-11-4-12-20-38/h1-22,25-26,29-30H,23-24,27-28H2 \n \nInChIKey = GYZZZILPVUYAFJ-UHFFFAOYSA-N \n \n \n \n \n \nPhysical Data: white solid, mp 222–226 °C. [α]d = −34 ± 4° (c 1, CHCl3). \n \n \n \n \n \n(S)-4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane [192463-40-4] \n \nInChI = 1S/C40H34P2/c1-5-13-35(14-6-1)41(36-15-7-2-8-16-36)39-29-31-21-25-33(39)27-23-32-22-26-34(28-24-31)40(30-32)42(37-17-9-3-10-18-37)38-19-11-4-12-20-38/h1-22,25-26,29-30H,23-24,27-28H2 \n \nInChIKey = GYZZZILPVUYAFJ-UHFFFAOYSA-N \n \n \n \n \n \nPhysical Data: white solid, mp 222–226 °C. [α]22d = +34° (c 1, CHCl3) \n \n \n \n(used as a chiral diphosphine ligand in transition metal-catalyzed reactions and also as organocatalyst) \n \n \n \nSolubility: not reported. \n \n \n \nForm Supplied in: white solid. Commercially available. \n \n \n \nHandling, Storage, and Precautions: readily oxidized to the phosphine oxide in solution and should be handled under N2 or Ar. Solid samples can be handled in air. Avoid contact with strong oxidizing agents and halogens.","PeriodicalId":11669,"journal":{"name":"Encyclopedia of Reagents for Organic Synthesis","volume":"54 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2012-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Encyclopedia of Reagents for Organic Synthesis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/047084289X.RN01475","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

(R)-4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane [364732-88-7] C40H34P2 (MW 576.65) InChI = 1S/C40H34P2/c1-5-13-35(14-6-1)41(36-15-7-2-8-16-36)39-29-31-21-25-33(39)27-23-32-22-26-34(28-24-31)40(30-32)42(37-17-9-3-10-18-37)38-19-11-4-12-20-38/h1-22,25-26,29-30H,23-24,27-28H2 InChIKey = GYZZZILPVUYAFJ-UHFFFAOYSA-N Physical Data: white solid, mp 222–226 °C. [α]d = −34 ± 4° (c 1, CHCl3). (S)-4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane [192463-40-4] InChI = 1S/C40H34P2/c1-5-13-35(14-6-1)41(36-15-7-2-8-16-36)39-29-31-21-25-33(39)27-23-32-22-26-34(28-24-31)40(30-32)42(37-17-9-3-10-18-37)38-19-11-4-12-20-38/h1-22,25-26,29-30H,23-24,27-28H2 InChIKey = GYZZZILPVUYAFJ-UHFFFAOYSA-N Physical Data: white solid, mp 222–226 °C. [α]22d = +34° (c 1, CHCl3) (used as a chiral diphosphine ligand in transition metal-catalyzed reactions and also as organocatalyst) Solubility: not reported. Form Supplied in: white solid. Commercially available. Handling, Storage, and Precautions: readily oxidized to the phosphine oxide in solution and should be handled under N2 or Ar. Solid samples can be handled in air. Avoid contact with strong oxidizing agents and halogens.
PhanePhos及其衍生物
(R)-4,12- bis (diphenylphosphino)-[2.2]-paracyclophane [364732-88-7] C40H34P2 (MW 576.65) InChI = 1S/C40H34P2/c1-5-13-35(14-6-1)41(36-15-7- 8-16-36)39-29-31-21-25-33(39)27-23-32- 32- 34(28-24-31)40(30-32)42(37-17-9-3-10-18-37)38-19-11-4-12-20-38/h1-22,25-26,29- 30h,23-24,27- 28h2 InChIKey = GYZZZILPVUYAFJ-UHFFFAOYSA-N物理数据:白色固体,mp 222-226°C。[α]d = - 34±4°(c1, CHCl3)。(S)-4,12- bis (diphenylphosphino)-[2.2]-paracyclophane [192463-40-4] InChI = 1S/C40H34P2/c1-5-13-35(14-6-1)41(36-15-7-2-8-16-36)39-29-31-21-25-33(39)27-23-32- 32- 34(28-24-31)40(30-32)42(37-17-9-3-10-18-37)38-19-11-4-12-20-38/ h2 -22,25-26,29- 30h,23-24,27- 28h2 InChIKey = GYZZZILPVUYAFJ-UHFFFAOYSA-N物理数据:白色固体,mp 222-226°C。[α]22d = +34°(c1, CHCl3)(用作过渡金属催化反应中的手性二膦配体,也用作有机催化剂)溶解度:未见报道。提供形式:白色固体。商业上可用。处理、储存和注意事项:在溶液中容易氧化为氧化膦,应在N2或Ar下处理。固体样品可在空气中处理。避免与强氧化剂和卤素接触。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信