CAS: 1125-78-6; 5,6,7,8-Tetrahydro-2-Naphthol

相似化合物

529-35-1 37827-68-2 303185-87-7

上下游产品

CAS号1730-48-9 6-甲氧基-1,2,3,4-四氢萘 | CAS号135-19-3 2-萘酚 | CAS号7440-44-0 活性炭 | CAS号119-64-2 1,2,3,4-四氢萘(THN) | CAS号77202-22-3 8a-hydroxy-3-(p... | CAS号1196-55-0 2(3H)-Naphthale... | CAS号872-36-6 碳酸亚乙烯酯 | CAS号871-84-1 1,7-辛二炔 | CAS号55705-17-4 α-(phenylsulfin... | CAS号493-01-6 萘烷 | CAS号493-02-7 反-十氢化萘 | CAS号5746-69-0 2-decalol | CAS号825-51-4 十氢-2-萘酚 | CAS号691892-19-0 2-Naphthalenol,... | CAS号40420-05-1 1-(3-羟基-5,6,7,8... | CAS号1878-59-7 2-(5,6,7,8-tetr... | CAS号22825-04-3 Naphthalene,6-e... | CAS号19015-68-0 5,6,7,8-tetrahy...

1,2,3,4-四氢萘置于硫酸体系中,化学反应生成5,6,7,8-四氢-2-萘酚
参考文献:De299603
标题:De299603

专利信息

专利号:US-2004110228-A1
优先权日:2002-04-01
标 题:Combinatorial organic synthesis of unique biologically active compounds
发明人：MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.

专利号:WO-2008103618-A1
优先权日:2007-02-22
标 题 :Synthesis of novel xylosides and potential uses thereof

专利号:GB-2193211-A
优先权日:1986-08-01
标题 :Synthesis of benzofurans

专利号:UA-78297-C2
优先权日:2002-04-10
标 题:1- or 3-thiabenzonaphlhoazulene as inhibitors of tumour necrosis factor production and intermediates for synthesis thereof

专利号:US-7638554-B2
优先权日:2002-04-18
标题 :Flavanoids as chemotherapeutic, chemopreventive, and antiangiogenic agents
发明人：WALEH NAHID; ZAVERI NURULAIN T
权利人:STANFORD RES INST INT
摘要:Compounds useful as chemotherapeutic, chemopreventive, and antiangiogenic agents are provided. The compounds are flavanoids, including flavanones, flavanols, and chalcones. The compounds have the structure of formula (I) n nwherein R 1 through R 3 and R 5 through R 11 are defined herein, and α, β and γ are optional bonds, providing that when α is absent, β is present, and when β is absent, α is present. When α is present, preferred R 4 moieties are selected from O, S, NH and CH 2 , and when α is absent, preferred R 4 groups are selected from OH, SH, NH 2 and CH 3 . When γ is present, the preferred R 5 substituent is O, while when γ is absent, the preferred R 5 substituent is OH. Pharmaceutical compositions are provided as well, as are methods of synthesis and use.

专利号:US-7329687-B2
优先权日:2002-04-18
标 题:Flavanoid compounds as chemotherapeutic, chemopreventive, and antiangiogenic agents
发明人：ZAVERI NURULAIN; CHAO WAN-RU
权利人:STANFORD RES INST INT
摘要:Compounds useful as chemotherapeutic, chemopreventive, and antiangiogenic agents are provided. The compounds are flavanoids, including flavanones, flavanols, and chalcones. The compounds have the structure of formula (I) n nwherein R 1 through R 3 and R 5 through R 11 are defined herein, and α, β, and γ are optional bonds, providing that when α is absent, β is present, and when β is absent, α is present. When α is present, preferred R 4 moieties are selected from O, S, NH and CH 2 , and when α is absent, preferred R 4 groups are selected from OH, SH, NH 2 and CH 3 . When γ is present, the preferred R 5 substituent is O, while when γ is absent, the preferred R 5 substituent is OH. Pharmaceutical compositions are provided as well, as are methods of synthesis and use.