✦ LIBER ✦

2-Amino-1,1,3-tricyanopropene: A new inhibitor of oxygen evolution in photosynthesis

✍ Scribed by A.A. Horton; D.O. Hall

Book ID: 115714815
Publisher: Elsevier Science
Year: 1967
Tongue: English
Weight: 188 KB
Volume: 131
Category: Article
ISSN: 0005-2728
DOI: 10.1016/0005-2728(67)90044-8

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

2-Amino-1,1,3-tricyanopropene in Heteroc

2-Amino-1,1,3-tricyanopropene in Heterocyclic Synthesis: Novel Synthesis of Thiopyran Pyridinethiones and Nicotinonitrile Derivatives

✍ Eldin, Abdellatif M. Salah 📂 Article 📅 2003 🏛 Taylor and Francis Group 🌐 English ⚖ 101 KB

3-Amino-1,4,5,6-tetrahydropyrrolo[3,4-c]

3-Amino-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazoles: A New Class of CDK2 Inhibitors.

✍ Paolo Pevarello; et al. et al. 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 19 KB 👁 1 views

3-Amino-1,4,5,6-tetrahydropyrrolo[3,4-c]

3-Amino-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazoles: A new class of CDK2 inhibitors

✍ Paolo Pevarello; Daniele Fancelli; Anna Vulpetti; Raffaella Amici; Manuela Villa 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 333 KB

ChemInform Abstract: A New, One-Pot, Mul

ChemInform Abstract: A New, One-Pot, Multi-Component Synthesis of Imines of 3-Amino-2-arylimidazo[1,2-a]pyridines, 3-Amino-2-arylimidazo[1,2-a]pyrazines, and 3-Amino-2-arylimidazo[1,2-a]pyrimidines.

✍ Mehdi Adib; Esmail Sheibani; Hamid Reza Bijanzadeh; Long-Guan Zhu 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 views

Cyclopent-4-ene-1,3-diones: A New Class

Cyclopent-4-ene-1,3-diones: A New Class of Herbicides Acting as Potent Photosynthesis Inhibitors

✍ Varejão, Jodieh O. S.; Barbosa, Luiz C. A.; Varejão, Eduardo V. V.; Maltha, Céli 📂 Article 📅 2014 🏛 American Chemical Society 🌐 English ⚖ 929 KB

A new enamine reaction: synthesis of 3-a

A new enamine reaction: synthesis of 3-amino-1,2-diazetidines

✍ L. Marchetti; G. Tosi 📂 Article 📅 1971 🏛 Elsevier Science 🌐 French ⚖ 215 KB

Cyclohexanone enamines react with dibenzoyldiimide (IIa) at room temperature leading to a I:1 addition product in almost quantitative yield. This adduct, on mild acidic hydrolysis, gives 2-(N,N'-dibenzoyl)hydrazinccyclohexanone (IVa), identical with that obtained from cyclohexanone and (IIa) at lOOa