-
1
-
-
33845556967
-
Stereochemistry of nucleophilic addition to cyclohexanone. The importance of two-electron stabilizing interactions
-
Cieplak, A. S., Stereochemistry of nucleophilic addition to cyclohexanone. The importance of two-electron stabilizing interactions. J. Am. Chem. Soc., 103, 4540-4552 (1981).
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 4540-4552
-
-
Cieplak, A.S.1
-
2
-
-
0003638901
-
-
McGraw-Hill Inc.
-
th edition, McGraw-Hill Inc., pp. 5.91-5.125 (1972).
-
(1972)
th Edition
-
-
-
3
-
-
0001403969
-
Asymmetric methoxyselenenylation of alkenes with chiral ferrocenylselenium reagents
-
Fukuzawa, S-I., Takahashi, K., Kato, H., and Yamazaki, H., Asymmetric methoxyselenenylation of alkenes with chiral ferrocenylselenium reagents. J. Org. Chem., 62, 7711-7716 (1997).
-
(1997)
J. Org. Chem.
, vol.62
, pp. 7711-7716
-
-
Fukuzawa, S.-I.1
Takahashi, K.2
Kato, H.3
Yamazaki, H.4
-
4
-
-
33845471903
-
Stereoselective nitrile oxide cycloadditions to chiral allyl ethers and alcohols. The inside alkoxy effect
-
Houk, K. N., Moses, S. R., Wu, Y. -D., Rondan, N. G., Jäger, V., Schohe, R., and Fronczek, F. R., Stereoselective nitrile oxide cycloadditions to chiral allyl ethers and alcohols. The inside alkoxy effect. J. Am. Chem. Soc., 106, 3880-3882 (1984).
-
(1984)
J. Am. Chem. Soc.
, vol.106
, pp. 3880-3882
-
-
Houk, K.N.1
Moses, S.R.2
Wu, Y.D.3
Rondan, N.G.4
Jäger, V.5
Schohe, R.6
Fronczek, F.R.7
-
6
-
-
0034576028
-
A novel synthetic method for α-amino acids from allyl ethers via N-allylcarbamates
-
Jung, Y. H. and Kim, J. D., A novel synthetic method for α-amino acids from allyl ethers via N-allylcarbamates. Arch. Pharm. Res., 23, 574-578 (2000).
-
(2000)
Arch. Pharm. Res.
, vol.23
, pp. 574-578
-
-
Jung, Y.H.1
Kim, J.D.2
-
7
-
-
0035487624
-
One-pot synthesis of cinnamylamines with various protecting groups from cinnamyl ethers
-
Jung, Y. H. and Kim, J. D., One-pot synthesis of cinnamylamines with various protecting groups from cinnamyl ethers. Arch. Pharm. Res., 24, 371-376 (2001).
-
(2001)
Arch. Pharm. Res.
, vol.24
, pp. 371-376
-
-
Jung, Y.H.1
Kim, J.D.2
-
8
-
-
30444457731
-
Mechanism studies on the CSI reaction with allyl ethers by varying p-substituent
-
Jung, Y. H. and Kim, J. D., Mechanism studies on the CSI reaction with allyl ethers by varying p-substituent. Arch. Pharm. Res., 26, 667-678 (2003)
-
(2003)
Arch. Pharm. Res.
, vol.26
, pp. 667-678
-
-
Jung, Y.H.1
Kim, J.D.2
-
9
-
-
0000473137
-
Novel synthetic method for N-allylcarbamates from allyl ethers using chlorosulfonyl Isocyanate
-
Kim, J. D., Lee, M. H., Lee, M. J., and Jung, Y. H., Novel synthetic method for N-allylcarbamates from allyl ethers using chlorosulfonyl Isocyanate. Tetrahedron Lett., 41, 5073-5076 (2000).
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 5073-5076
-
-
Kim, J.D.1
Lee, M.H.2
Lee, M.J.3
Jung, Y.H.4
-
10
-
-
0035944158
-
Synthesis of N-protected allylic amines from allyl ethers
-
Kim, J. D., Lee, M. H., Han, G., Park, H., Zee, O. P., and Jung, Y. H., Synthesis of N-protected allylic amines from allyl ethers. Tetrahedron, 57, 8257-8266 (2001).
-
(2001)
Tetrahedron
, vol.57
, pp. 8257-8266
-
-
Kim, J.D.1
Lee, M.H.2
Han, G.3
Park, H.4
Zee, O.P.5
Jung, Y.H.6
-
11
-
-
0037182033
-
Study of the stability of carbocations by chlorosulfonyl isocyanate reaction with ethers
-
Kim, J. D., Han, G., Jeong, L. S., Park, H. -J., Zee, O. P., and Jung, Y. H., Study of the stability of carbocations by chlorosulfonyl isocyanate reaction with ethers. Tetrahedron, 58, 4395-4402 (2002).
-
(2002)
Tetrahedron
, vol.58
, pp. 4395-4402
-
-
Kim, J.D.1
Han, G.2
Jeong, L.S.3
Park, H.J.4
Zee, O.P.5
Jung, Y.H.6
-
12
-
-
0037455037
-
Deprotection of benzyl and p-methoxybenzyl ethers by chlorosulfonyl isocyanate-sodium hydroxide
-
Kim, J. D., Han, G., Zee, O. P., and Jung, Y. H., Deprotection of benzyl and p-methoxybenzyl ethers by chlorosulfonyl isocyanate-sodium hydroxide. Tetrahedron Lett., 44, 733-735 (2003).
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 733-735
-
-
Kim, J.D.1
Han, G.2
Zee, O.P.3
Jung, Y.H.4
-
13
-
-
0037414555
-
Regioselective and diastereoselective allylic amination using chlorosulfonyl isocyanate. A novel asymmetric synthesis of unsaturated aromatic 1,2-amino alcohols
-
Kim, J. D., Zee, O. P., and Jung, Y. H., Regioselective and diastereoselective allylic amination using chlorosulfonyl isocyanate. A novel asymmetric synthesis of unsaturated aromatic 1,2-amino alcohols. J. Org. Chem., 68, 3721-3724 (2003).
-
(2003)
J. Org. Chem.
, vol.68
, pp. 3721-3724
-
-
Kim, J.D.1
Zee, O.P.2
Jung, Y.H.3
-
14
-
-
12344308337
-
Diastereoselective synthesis of unsaturated 1,2-amino alcohols from a-hydroxy allyl ethers using chlorosulfonyl isocyanate
-
in press
-
Kim, J. D., Kim, I. S., Jin, C. H., Zee, O. P., and Jung, Y. H., Diastereoselective synthesis of unsaturated 1,2-amino alcohols from a-hydroxy allyl ethers using chlorosulfonyl isocyanate. Tetrahedron Lett., in press (2005).
-
(2005)
Tetrahedron Lett.
-
-
Kim, J.D.1
Kim, I.S.2
Jin, C.H.3
Zee, O.P.4
Jung, Y.H.5
-
15
-
-
0003467672
-
-
John Wiley & Sons Inc.
-
th edition, John Wiley & Sons Inc., pp. 326-327 (1992).
-
(1992)
th Edition
, pp. 326-327
-
-
March, J.1
-
16
-
-
0034607882
-
Structures of cribochalines A and B, branched-chain methoxylaminoalkyl pyridines from the micronesian sponge, Cribochalina sp. Absolute configuration and enantiomeric purity of related O-methyl oximes
-
Nicholas, G. M. and Molinski, T. F., Structures of cribochalines A and B, branched-chain methoxylaminoalkyl pyridines from the micronesian sponge, Cribochalina sp. Absolute configuration and enantiomeric purity of related O-methyl oximes. Tetrahedron, 56, 2921-2927 (2000).
-
(2000)
Tetrahedron
, vol.56
, pp. 2921-2927
-
-
Nicholas, G.M.1
Molinski, T.F.2
-
17
-
-
0003466757
-
-
Longman Scientific & Technical, Singapore
-
th edition, Longman Scientific & Technical, Singapore, pp. 90-93 (1986).
-
(1986)
th Edition
, pp. 90-93
-
-
Sykes, P.1
-
18
-
-
0037453335
-
First synthesis of (1S, 2S)- and (1R, 2R)-1-amino-2- isopropylcyclobutanecarboxylic acids by asymmetric Strecker reaction from 2-substituted cyclobutanones
-
Truong, M., Lecornué, F., and Fadel, A., First synthesis of (1S, 2S)- and (1R, 2R)-1-amino-2-isopropylcyclobutanecarboxylic acids by asymmetric Strecker reaction from 2-substituted cyclobutanones. Tetrahedron: Asymmetry, 14, 1063-1072 (2003).
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 1063-1072
-
-
Truong, M.1
Lecornué, F.2
Fadel, A.3
-
19
-
-
0001562620
-
Diastereoselectivity of the conjugate addition of organocopper reagents to γ-alkoxy-α,β-unsaturated carbonyl derivatives. Importance of the reagent type and the doublebond geometry
-
Yamamoto, Y., Chounan, Y., Nishii, S., Ibuka, T., and Kitahara, H., Diastereoselectivity of the conjugate addition of organocopper reagents to γ-alkoxy-α,β-unsaturated carbonyl derivatives. Importance of the reagent type and the doublebond geometry. J. Am. Chem. Soc., 114, 7652-7660 (1992).
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 7652-7660
-
-
Yamamoto, Y.1
Chounan, Y.2
Nishii, S.3
Ibuka, T.4
Kitahara, H.5
-
20
-
-
0022403658
-
Total synthesis of acosamine and daunosamine utilizing a diastereoselective intramolecular [3+2] cycloaddition
-
Wovkulich, P. M. and Uskokovic, M. R., Total synthesis of acosamine and daunosamine utilizing a diastereoselective intramolecular [3+2] cycloaddition. Tetrahedron, 41, 3455 (1985).
-
(1985)
Tetrahedron
, vol.41
, pp. 3455
-
-
Wovkulich, P.M.1
Uskokovic, M.R.2
|