CAS: 1100-88-5; Benzyltriphenylphosphonium Chloride

相似化合物

1449-46-3 1530-37-6 1530-39-8

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CAS号100-44-7 氯化苄 | CAS号603-35-0 三苯基膦 | CAS号5293-84-5 (氯甲基)三苯基氯化磷 | CAS号110637-73-5 Benzyltriphenyl... | CAS号56-93-9 苄基三甲基氯化铵 | CAS号1449-46-3 苄基三苯基溴化膦 | CAS号100-39-0 溴化苄 | CAS号100-51-6 苯甲醇 | CAS号106664-91-9 3-(苄基磺酰基)-2-甲基丙酸 | CAS号13041-70-8 反-4-溴二苯乙烯 | CAS号4714-24-3 4-溴均二苯乙烯 | CAS号791-28-6 三苯基氧化膦 | CAS号14310-22-6 1-chloro-4-(2-p... | CAS号4714-21-0 4-甲基二苯乙烯 | CAS号873-66-5 反-β-甲基苯乙烯 | CAS号766-90-5 顺-β-甲基苯乙烯 | CAS号886-65-7 1,4-二苯基1,3-丁二烯

[α-(Phenylphosphanyl)Benzylidene]Triphenylphosphorane置于盐酸体系中,用 四氢呋喃,乙醚 用作溶剂,化学反应 0.5H,反应生成苄基三苯基氯化膦
参考文献:Ylidylphosphanes 和-Diphosphanes
标题:Ylidylphosphanes 和-Diphosphanes
摘要:氯膦酰基和二氯膦酰基亚烷基-和亚苄基膦 6 和 8 通过与 Lialh4 反应转化为相应的膦 7 和 9.前者可以被分离出来,但在加热或质子化时会分解,得到亚丙基二膦 11 和鏻叶立德或鏻盐,分别.最终产品是环寡膦 15-17.只有 C-叔丁基衍生物 7C 在这两个方面都是稳定的.与6中rpc1组的构象相比,7中rph基团的构象清楚地反映了它们与叶立德部分的不同相互作用.
Doi:10.1002/(Sici)1099-0682(199803)1998:3<381::Aid-Ejic381>3.0.Co;2-L

专利信息

专利号:US-2008103312-A1
优先权日:2006-08-29
标 题:Processes for the synthesis of 5-phenyl-1-trityl-1H-tetrazole
发明人：KANSAL VINOD K; MISTRY DHIRENKUMAR N; VASOYA SANJAY L; LUNAGARIYA VIJAYKUMAR D
权利人:KANSAL VINOD K; MISTRY DHIRENKUMAR N; VASOYA SANJAY L; LUNAGARIYA VIJAYKUMAR D
摘要:Provided are processes for the synthesis of 5-phenyl-1-trityl-1H-tetrazole, an intermediate useful in the synthesis of irbesartan.

专利号:US-2002042514-A1
优先权日:2000-06-26
标 题 :Synthesis of chlorinated pyrimidines
发明人：DOYLE TIMOTHY JOHN; WEHRENBERG PETER KARL; STANDEN MICHAEL CHARLES HENRY
摘要:A facile process for the preparation of 4,6-dichloropyrimidine is provided, which utilizes quaternary ammonium salts or quaternary phosphonium salts as catalysts for the reaction of, for example, 4,6-dihydroxypyrimidine or 4-chloro-6-methoxypyrimidine with phosgene.

专利号:EP-0830136-B1
优先权日:1995-03-07
标 题:New cryptophycins from synthesis
发明人：MOORE RICHARD E; TIUS MARCUS A; BARROW RUSSELL A; LIANG JIAN; CORBETT THOMAS H; VALERIOTE FREDERICK A; HEMSCHEIDT THOMAS K; GOLAKOTI TRIMURTULU
权利人:UNIV HAWAII; UNIV WAYNE STATE
摘要:Novel cryptophycin compounds are disclosed, together with methods of producing cryptophycins by total synthesis and methods for the use of such cryptophycins in pharmaceuticals to inhibit the proliferation of mammalian cells and to treat neoplasia.

专利号:US-6204361-B1
优先权日:1996-01-18
标 题 :Method of peptide synthesis
发明人：CARPINO LOUIS A; IONESCU DUMITRU
权利人:RES CORP TECHNOLOGIES INC
摘要:The present invention relates to a process for forming an N-α-amino protected amino acid fluoride in situ by reacting an N-α-amino protected amino acid with an ionic fluoride salt in the presence of a peptide coupling agent. It is also directed to the use of the amino acid fluoride thus formed in peptide synthesis.

专利号:US-6013626-A
优先权日:1993-12-21
标题 :Cryptophycins from synthesis
发明人：MOORE RICHARD E; TIUS MARCUS A; BARROW RUSSELL A; LIANG JIAN; CORBETT THOMAS H; VALERIOTE FREDERICK A; GOLAKOTI TRIMURTULU; HEMSCHEIDT THOMAS K
权利人:UNIV HAWAII; UNIV WAYNE STATE
摘要:A cryptophycin compound is provided having the structure: ##STR1## Further provided are methods of producing cryptophycins by total synthesis and methods of using cryptophycins in pharmaceuticals. It is a further object of this invention to use cryptophycins to inhibit the proliferation of mammalian cells. Moreover, methods of using cryptophycins to treat neoplasia is also provided.

专利号:US-8809585-B2
优先权日:2004-10-02
标 题:Synthesis scheme for lacosamide
发明人：RIEDNER JENS; DUNNE GAVIN
权利人:RIEDNER JENS; DUNNE GAVIN; UCB PHARMA GMBH
摘要:The present invention is concerned with an improved method of producing (R)-2-acetamido-N-benzyl-3-methoxypropionamide (lacosamide) comprising the 0-methylation of a compound of formula (I) to produce a compound of formula (II) in a single step reaction.