Download e-book for iPad: Annual Reports in Organic Synthesis–1975 by R. Bryan Miller, L. G. Wade

By R. Bryan Miller, L. G. Wade

ISBN-10: 0120408066

ISBN-13: 9780120408061

Annual reviews in natural Synthesis – 1975 is a set of helpful information regarding the developments within the box of natural chemistry. acknowledged info is gifted within the kind of images and/or natural chemistry equations.
The publication covers issues resembling carbon-carbon bond forming reactions; oxidations; savings; synthesis of heterocycles; artificial arrangements; and different miscellaneous reactions. The monograph is suggested for natural chemists who want to recognize extra concerning the developments within the box with no the necessity to learn large texts.

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Extra resources for Annual Reports in Organic Synthesis–1975

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T. la-19 M. S. Chem. , 1975. 289. 1) n-BuLi, THF . (MeC0) 2 C= SMe 2 2) RCÖC1 *" SMe 9 II i RC0CH2C0CC0Me R = Ph, 55% R = OEt, 68% The = S M e 2 group can be removed by Zn-HOAc. la-20 T. Izawa and T. Mukaiyama, Chem. , 1975. 161. la-21 319. I^CHiOR2^ T. Mukaiyama and A. Ishida, Chem. L e t t . , 1975. la-22 E. Kitazawa, T. Imamura, K. Saigo, and T. Mukaiyama, Chem. L e t t . , 1975. 569. la-23 741. ,? S i M % ll ->? R C=CHR^ K. Banno and T. Mukaiyama, Chem. L e t t . , 1975, o Λ MeC0(CR R ) C0,Et " C + 1) T i C l / , , CH~C1~ c c > 2) H 2 0 OH 1 R COCHR2CMe(CR3R4)nC02Et R1 R2 R3 R4 n Et Me - - 0 87 Ph H - - 0 63 4CH2)-4 - - 0 88 4CH2)-4 Me Me 1 52 ■ ( ( H H 2 73 ;H 2*3 % Yield I .

E. Baldwin, and 0. W. , J. C. S. Chem. , 1975, 519. 5-17 K. Oshima, H. Yamamoto, and H. Nozaki, Bull. Chem. Soc. Japan, 48, 1567 (1975). i-PrSCH2CH=CH2 l)s-ßuLi, Et 2 0, -25C 2)CuI> _ 7 8 6 3)R 1 R 2 C=CR 3 CH 2 Br "> i-PrSCH=CHCH 2 CR ] R 2 CR 3 =CH 2 R1 R2 R3 % Yield H H H 88 H 92 4CH2>5 « 1 -(CH 2*4 87 l)s-BuLi, Et ? 5-18 Y. Kitagawa, K. Oshima, H. Yamamoto, and H. , 1975, 1859. ,, , The effect of R^NLi on the product distribution was studied. 5-19 J. Normant, G. Cahiez, and J. Villieras, J.

Forner, and T. Müller, 1. , 15, 15 (1975). la-15 1975. 589. , 9 R R^C=CHC0R K. K. J. la-16 T. Tanaka, S. Kurozumi, T. Toru, M. Kobayashi, S. Miura, and S. , 1975. 1535. P — E t 2 0 , HHPA, - W 2) RX0C1 > COfT | ? la-17 1975. 1876. R. Nouri-Bimorghi, Bull. Soc. Chim. la-18 G. Stork and M. Isobe, J. Am. Chem. , 27, 4745 (1975); see also: ibid, 92, 6260 (1975). t. la-19 M. S. Chem. , 1975. 289. 1) n-BuLi, THF . (MeC0) 2 C= SMe 2 2) RCÖC1 *" SMe 9 II i RC0CH2C0CC0Me R = Ph, 55% R = OEt, 68% The = S M e 2 group can be removed by Zn-HOAc.

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Annual Reports in Organic Synthesis–1975 by R. Bryan Miller, L. G. Wade


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