✦ LIBER ✦

Is carbon suboxide a new candidate as starting material for the synthesis of biomolecules on the primitive earth?

✍ Scribed by YANAGAWA, H; EGAMI, F

Book ID: 123347467
Publisher: Elsevier Science
Year: 1981
Tongue: English
Weight: 359 KB
Volume: 14
Category: Article
ISSN: 0301-9268
DOI: 10.1016/0301-9268(81)90036-X

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and Isolation of Di- n -butylh

Synthesis and Isolation of Di- n -butylhafnocene and Its Application as a Versatile Starting Material for the Synthesis of New Hafnacycles

✍ Burlakov, Vladimir V.; Beweries, Torsten; Bogdanov, Vyacheslav S.; Arndt, Perdit 📂 Article 📅 2009 🏛 American Chemical Society 🌐 English ⚖ 158 KB

Bis ( O -nitrophenyl) Carbonate as a New

Bis ( O -nitrophenyl) Carbonate as a New Reagent for the Synthesis of Chiral Oxazolidin-2-ones

✍ Simon, Monika; Micle, Andreea; Badea, Valentin; Csunderlik, Carol 📂 Article 📅 2009 🏛 Taylor and Francis Group 🌐 English ⚖ 146 KB

ChemInform Abstract: Bis(O-nitrophenyl)

ChemInform Abstract: Bis(O-nitrophenyl) Carbonate as a New Reagent for the Synthesis of Chiral Oxazolidin-2-ones.

✍ Monika Simon; Andreea Micle; Valentin Badea; Carol Csunderlik 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 17 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

A New Method for Synthesis of α,α-Disubs

A New Method for Synthesis of α,α-Disubstituted Carbonyl Compounds from Carbonyl Compounds with One-Carbon Homologation Through β-Oxido Carbenoid Rearrangement as the Key Reaction.

✍ Kohsuke Miyashita; Tsuyoshi Satoh 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

A New Method for Synthesis of α,α-Disubs

A New Method for Synthesis of α,α-Disubstituted Carbonyl Compounds from Carbonyl Compounds with One-Carbon Homologation Through β-Oxido Carbenoid Rearrangement as the Key Reaction.

✍ Kohsuke Miyashita; Tsuyoshi Satoh 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

Development of two processes for the syn

Development of two processes for the synthesis of bridged azabicyclic systems: intermolecular radical addition?homoallylic rearrangements leading to 2-azanorborn-5-enes and neophyl-type radical rearrangements to 2-azabenzonorbornanesThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current academic staff move across South Parks Road to a new purpose-built laboratory.Electronic supplementary information (ESI) available: the preparation and characterisation of compounds 20b?i, 28c?g, 30b?g, 30i, 32e?g, 32i, 33b?g. See http//www.rsc.org/suppdata/ob/b3/b306717n/

✍ Hodgson, David M.; Bebbington, Magnus W. P.; Willis, Paul 📂 Article 📅 2003 🏛 Royal Society of Chemistry 🌐 English ⚖ 276 KB