Results
1 -
10 of
13
(Click
here to explore results)
- The diastereoselectivity of electrophilic attack on trigonal carbon adjacent to a stereogenic centre: diastereoselective alkylation and protonation of open-chain enolates having a stereogenic centre carrying a silyl group at the β position. Roger A. N. C. Crump, Ian Fleming, John H. M. Hill, David Parker, N. Laxma Reddy, David Waterson
, J. Chem. Soc., Perkin Trans. 1
, 1992
, 3277
- A study on the AMACR catalysed elimination reaction and its application to inhibitor testing. Maksims Yevglevskis, Guat L. Lee, Jenny Sun, Shiyi Zhou, Xiaolong Sun, Gabriele Kociok-Köhn, Tony D. James, Timothy J. Woodman, Matthew D. Lloyd
, Org. Biomol. Chem.
, 2016
, 14
, 612
- AlCl3 catalyzed coupling of N-benzylic sulfonamides with 2-substituted cyanoacetates through carbon–nitrogen bond cleavage. Chen Hu, Gang Hong, Xiaofei Qian, Kwang Rim Kim, Xiaoyan Zhu, Limin Wang
, Org. Biomol. Chem.
, 2017
, 15
, 4984
- The stereoselective synthesis of oxetanes; exploration of a new, Mitsunobu-style procedure for the cyclisation of 1,3-diols. Martin Christlieb, John E. Davies, Jason Eames, Richard Hooley, Stuart Warren
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 2983
- Specific inhibitors in vitamin biosynthesis. Part 7. Syntheses of blocked 7,8-dihydropteridines viaα-amino ketones. Saiba S. Al-Hassan, Robert J. Cameron, Adrian W. C. Curran, William J. S. Lyall, Sydney H. Nicholson, David R. Robinson, Alexander Stuart, Colin J. Suckling, Irene Stirling, Hamish C. S. Wood
, J. Chem. Soc., Perkin Trans. 1
, 1985
, 1645
- A synthesis of allylsilanes in which the silyl group is at the more-substituted end of the allyl group. Ian Fleming, David Waterson
, J. Chem. Soc., Perkin Trans. 1
, 1984
, 1809
- Atropisomeric benzamides and naphthamides as chiral auxiliaries. Jonathan Clayden, Madeleine Helliwell, Catherine McCarthy, Neil Westlund
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 3232
- Ti-direct, powerful, stereoselective aldol-type additions of esters and thioesters to carbonyl compounds: application to the synthesis and evaluation of lactone analogs of jasmone perfumes. Ryohei Nagase, Noriaki Matsumoto, Kohei Hosomi, Takahiro Higashi, Syunsuke Funakoshi, Tomonori Misaki, Yoo Tanabe
, Org. Biomol. Chem.
, 2007
, 5
, 151
- A facile preparation of indium enolates and their Reformatsky- and Darzens-type reactions. Tsunehisa Hirashita, Kenji Kinoshita, Hatsuo Yamamura, Masao Kawai, Shuki Araki
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 825
- Asymmetric synthesis of syn-α-alkyl-β-amino acids. Stephen G. Davies, Osamu Ichihara, Iain A. S. Walters
, J. Chem. Soc., Perkin Trans. 1
, 1994
, 1141