26732-07-0Relevant academic research and scientific papers
Gold(III)-catalyzed synthesis of 2,5-disubstituted furans from substituted 5-methoxyhex-3-yn-2-ols—Mechanistic outlook
Behera, Sagarika,Bera, Nabakumar,Sarkar, Debayan
, p. 3090 - 3098 (2021/08/12)
Gold(III)-catalyzed activation of alkynes has been applied for the synthesis of 2,5-disubstituted furans from substituted 5-methoxy-hex-3-yn-2-ols. Mechanistically, the reaction proceeds via an allenyl carbocation intermediate followed by 5-endo-dig cyclization. The high-yielding, open-air, room temperature reaction conditions applied to synthesize a series of alkyl, aryl, and hetero aryl-substituted furans provide uniqueness to the strategy.
Successively recycle waste as catalyst: A one-pot wittig/1,4-reduction/paal-knorr sequence for modular synthesis of substituted furans
Chen, Long,Du, Yi,Zeng, Xing-Ping,Shi, Tao-Da,Zhou, Feng,Zhou, Jian
supporting information, p. 1557 - 1560 (2015/03/30)
A one-pot tandem Wittig/conjugate reduction/Paal-Knorr reaction is reported for the synthesis of di- or trisubstituted furans. This novel sequence first demonstrates the possibility of successively recycling waste from upstream steps to catalyze downstream reactions.
The Photochemistry of α,β-Acetylenic Ketones. II. Formation of Furan Derivatives
Nishio, Takehiko,Nakata, Hiroyuki,Omote, Yoshimori
, p. 1011 - 1013 (2007/10/02)
The phochemical reactions of α,β-acetylenic ketones have been examined.Irradiation of 1-p-substituted phenyl-2-propyn-1-ones 2-4 in primary alcohols gave 2,5-disubstituted furans 2a-4c.The formation of furans can be explained in terms of cyclization, foll
A NOVEL PALLADIUM-CATALYZED REARRANGEMENT OF ACETYLENIC KETONES TO FURANS
Sheng, Huaiyu,Lin, Shouyuan,Huang, Yaozeng
, p. 4893 - 4894 (2007/10/02)
A novel rearrangement of 1-aryl-4-alkyl-2-butyn-1-one in the presence of Pd(dba)2-PPh3 catalyst gave 2,4-substituted furans in moderate yields.
