A NEW ENTRY TO THE SYNTHESIS OF PRIMIN VIA A B-ALKYL SUZUKI–MIYAURA CROSS-COUPLING REACTION (Dedicated to Professor Dr. Ei-ichi Negishi on the occasion of his 77th birthday)
暂无分享,去创建一个
[1] Koichi Narita,et al. Total Synthesis of Bauhinoxepin J: A Biologically Active Dibenzo[b,f]oxepin Isolated from Bauhinia purpurea , 2011 .
[2] Tanpreet Kaur,et al. Synthesis of the AntibacterialBenzoquinone Primin and its Water-Soluble Analogue, Primin Acid , 2010 .
[3] H. Abe,et al. Highly efficient total synthesis of the marine natural products (+)-avarone, (+)-avarol, (-)-neoavarone, (-)-neoavarol and (+)-aureol. , 2008, Chemistry.
[4] J. Sakayaroj,et al. A new dihydrobenzofuran derivative from the endophytic fungus Botryosphaeria mamane PSU-M76. , 2007, Chemical & pharmaceutical bulletin.
[5] V. Yardley,et al. Antituberculotic and Antiprotozoal Activities of Primin, a Natural Benzoquinone: In vitro and in vivo Studies , 2006, Chemistry & biodiversity.
[6] C. Moody,et al. Microwave-assisted combined Mitsunobu reaction–Claisen rearrangement and microwave-assisted phenol oxidation: rapid synthesis of 2,6-disubstituted-1,4-benzoquinone natural products , 2005 .
[7] Timothy E. Hurst,et al. Microwave-mediated Claisen rearrangement followed by phenol oxidation: a simple route to naturally occurring 1,4-benzoquinones. The first syntheses of verapliquinones A and B and panicein A. , 2005, The Journal of organic chemistry.
[8] T. Katoh,et al. Highly Improved Synthesis of (+)-Aureol via (-)-Neoavarone and (-)-Neoavarol, by Employing Salcomine Oxidation and Acid-Induced Rearrangement/Cyclization Strategy , 2003 .
[9] C. Moody,et al. The Claisen Rearrangement Followed by Phenol Oxidation: A Simple Route to Naturally Occurring Benzoquinones Including an Ansa-Bridged Derivative Related to the Ansamycin Antibiotics , 2002 .
[10] T. Katoh,et al. An efficient synthesis of (+)-aureol via boron trifluoride etherate-promoted rearrangement of (+)-arenarol , 2002 .
[11] O. Ohmori,et al. Studies toward the Total Synthesis of Popolohuanone E: Enantioselective Synthesis of 8-O-MethylpopolohuanoneE , 2001 .
[12] C. Benezra,et al. New Syntheses of the Benzoquinone Primin and its Water-Soluble Analog Primin Acid via Heck Reactions , 1999 .
[13] S. S. Arogba. SYNTHESIS OF PRIMIN AND MICONIDIN AND THEIR 3-METHOXY ISOMERS , 1991 .
[14] L. Bieber,et al. Simple Synthesis of Primin and its Analogues via Lithiation of Protected Guaiacol , 1990 .
[15] Antoni Costa,et al. Metalation of phenols. Synthesis of benzoquinones by the oxidative degradation approach , 1988 .
[16] J. Morey,et al. A novel degradative strategy for the synthesis of p-quinones. , 1987 .
[17] J. Morey,et al. Oxidative degradation approach to p-quinones , 1986 .
[18] E. Bernays,et al. Antifeedant nature of the quinone primin and its quinol miconidin fromMiconia spp , 1984, Experientia.
[19] D. Kingston,et al. Isolation, synthesis, and structure-activity relationships of bioactive benzoquinones from Miconia lepidota from the Suriname rainforest. , 2001, Journal of natural products.
[20] J. M. Saa,et al. On the regioselectivity of the fremy's salt oxidation of phenols , 1987 .