在常温常压下稳定,应避免接触氧化物。
中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
—— | (2E)-octa-2,7-dien-1-ol | 62179-18-4 | C8H14O | 126.199 |
2-辛烯酸 | trans-2-octenoic acid | 1871-67-6 | C8H14O2 | 142.198 |
反-2-辛烯醛 | (E)-2-Octenal | 2548-87-0 | C8H14O | 126.199 |
中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
—— | trans-2-octenyl methyl ether | 62179-15-1 | C9H18O | 142.241 |
(4E)-4-癸烯-1-醇 | (E)-4-decen-1-ol | 10339-62-5 | C10H20O | 156.268 |
顺-2-辛烯 | cis-2-octene | 7642-04-8 | C8H16 | 112.215 |
反-2-辛烯 | (E)-Oct-2-ene | 13389-42-9 | C8H16 | 112.215 |
—— | 1-vinyloxy-oct-2-ene | 70396-75-7 | C10H18O | 154.252 |
2-辛烯酸 | trans-2-octenoic acid | 1871-67-6 | C8H14O2 | 142.198 |
—— | (3E,6E)-3,6-dodecadien-1-ol | 116264-82-5 | C12H22O | 182.306 |
十一碳-1,5-二烯 | (Z)-1,5-undecadiene | 106051-44-9 | C11H20 | 152.28 |
—— | (5E)-undeca-1,5-diene | 106051-45-0 | C11H20 | 152.28 |
7-十四碳烯-1-醇 | (7E)-tetradec-7-en-1-ol | 37011-95-3 | C14H28O | 212.376 |
—— | trans-hexadec-9-en-1-ol | 64437-47-4 | C16H32O | 240.429 |
—— | (E)-non-3-enoic acid | 28163-88-4 | C9H16O2 | 156.225 |
(3Z)-3-壬烯酸 | (Z)-non-3-enoic acid | 41653-98-9 | C9H16O2 | 156.225 |
3-壬烯酸 | 3-nonenoic acid | 4124-88-3 | C9H16O2 | 156.225 |
—— | (E)-1-chlorooct-2-ene | 68883-76-1 | C8H15Cl | 146.66 |
—— | (E)-1-iodooct-2-ene | 74962-71-3 | C8H15I | 238.112 |
—— | (E)-2-octen-1-ylamine | 70729-20-3 | C8H17N | 127.23 |
2-辛烯醛 | 2-octen-1-al | 2363-89-5 | C8H14O | 126.199 |
—— | (E)-1-bromo-oct-2-ene | 56318-83-3 | C8H15Br | 191.111 |
反-2-辛烯醛 | (E)-2-Octenal | 2548-87-0 | C8H14O | 126.199 |
—— | (E)-1-fluorooct-2-ene | 1422173-21-4 | C8H15F | 130.206 |
反-4-癸烯醛 | trans-4-decenal | 65405-70-1 | C10H18O | 154.252 |
—— | (Z)-3-iodo-2-octen-1-ol | 63093-31-2 | C8H15IO | 254.111 |
(E)-辛-2-烯基乙酸酯 | (E)-2-octen-1-yl acetate | 3913-80-2 | C10H18O2 | 170.252 |
—— | 1-Acetoxy-octen-(2) | 2371-13-3 | C10H18O2 | 170.252 |
Bestmann ylide [(triphenylphosphoranylidene)ketene] acts as a chemical linchpin that links nucleophilic entities, such as alcohols or amines, with carbonyl moieties to produce unsaturated esters and amides, respectively. In this work, the formation of α,β,γ,δ-unsaturated esters (dienoates) is achieved through the coupling of Bestmann ylide, an alcohol and an α,β-unsaturated aldehyde. Primary and secondary alcohols, including allylic alcohols, are suitable substrates; the newly formed alkene has an