Fiesers' Reagents for Organic Synthesis (Volume 17) by Mary Fieser

By Mary Fieser

From stories of past volumes: "Essential for chemistry collections on the collage and learn levels." --New York Public Library ".highly recommended.lots of succinct, functional details on fresh developments.in a layout that's effortless to take advantage of. The reagents are taken up in alphabetical order (common utilization names, no longer CAS indexing code names), occasionally a number of to a web page, occasionally a number of pages to a reagent. it is easy to look forward to finding tips to make the reagent (in free terms), or the place it may be acquired, what it's stable for, and the place to hunt whole details.As with prior volumes, you can still make the most of simply looking, no matter if one doesn't think a necessity to appear up any specific topic. it's therefore a secondary functionality of the e-book to assist one maintain abreast of the sphere, and it might be a unprecedented chemist who wouldn't research anything new and important from an informal perusal of the pages." --Journal of the yankee Chemical Society Reagents for natural Synthesis quantity 1 1967 (0-471-25875-X) 1,475 pp. quantity 2 1969 (0-471-25876-8) 538 pp. quantity three 1972 (0-471-25879-2) 401 pp. quantity four 1974 (0-471-25881-4) 660 pp. quantity five 1975 (0-471-25882-2) 864 pp. quantity 6 1977 (0-471-25873-3) 765 pp. quantity 7 1979 (0-471-02918-1 ) 487 pp. quantity eight 1980 (0-471-04834-8) 602 pp. quantity nine 1981 (0-471-05631-6) 596 pp. quantity 10 1982 (0-471-86636-9) 528 pp. quantity eleven 1984 (0-471-88628-9) 669 pp. quantity 12 1986 (0-471-83469-6) 643 pp. quantity thirteen 1988 (0-471-63007-1) 472 pp. quantity 14 1989 (0-471-50400-9) 386 pp. quantity 15 1990 (0-471-52113-2) 432 pp. quantity sixteen 1992 (0-471-52721-1) 435 pp.

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C'5. Chem. Y. Murahashi, S. Aoki, M. Takano,T. ,1559 (1'991). 2T. Hosokawa,M. Takano,Y. Murahashi,Tetrahedron Letters,33,6643 (1992). ,cH3 Fl: O ,iJfhvdc (2) Bis[(allyl)trifl uoroacetato]nickel(II)' 1. Attempts to polymerize phenylenesdirectly results in mixtures of para-, meta-, and ortho-linkedoligomers. In contrastpolymerizationof cls2 with I in CcHsCI results in exclusive 5,6-bis(trimethylsilyloxy)-1,3-cyclohexadiene 3. This polymer is convertedinto poly(pformation of the 1,4-poly-1,3-cyclohexadiene phenylene)(5) by conversionof the trimethylsilyloxy groups to acetyl groups followed by pyrolysis.

S . H w a n g , W . J . K i m , a n d J . K . L i m , T e t r a h e d r o n L e t t e r s , 3 24' 0 1 5 ( 1 9 9 1 ) ' * ith LiOH I >iX)n ricld under 3 atm r*\ used to d or onll proi J E. ,ll (E)-squalene -\ Yanagtsawa, t-. F: 27 Benzylchlorobis(triphenylphosphine) palladium(II). Stille macrocyclization. Several macrocylic antibiotics contain a y-oxo-a,Bunsaturatedestergroup. Selectivesaponificationof the methyl ester R I R o ll r{ -o- '\I P(c6H5)3, -c_,. , r _ o . c rDEAD . Hol\1cHr)ecH2coocH3 "H-COOH vvv'7/' -1cHr)ecH2coocH3 H.

Helmchen. : ll. J. Corel and ' D. A. 3 The chiral bis(oxazoline) 1, preparedfrom (2) serves (S)-phenylglycine,in combinationwith MgI2 or magnesiumtetraphenylborate of cyclopentadiene reaction for the Diels-Alder catalyst as a highly enantioselective with 3-acryloyloxazolidine-2-one(equationI). r,ro#o\-cH. /Wiv ru-/-cs. O#&":j, g ? 1:JJhY reactron \\ hcn present in with ethyl diazoacetate. ::rdrosilYlation P--\o.. -N '-I (cH3)3c c(cH3)3 1 o\, fi c6H5 cH, + N2cHcooc2H5 r, cHct3 -CHa i c . t highestenans.

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Fiesers' Reagents for Organic Synthesis (Volume 17) by Mary Fieser
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