| Year |
Citation |
Score |
| 2023 |
Kawasaki Y, Hayashibara T, Seto Y, Taniguchi Y, Igawa K, Tomooka K. Development of DACN-NHS-ester and DACN-maleimide, and their application for the synthesis of artificial hybrid biomolecules. Chemical Communications (Cambridge, England). 59: 11724-11727. PMID 37702377 DOI: 10.1039/d3cc03023g |
0.344 |
|
| 2019 |
Tomooka K, Yamamoto K, Nakai T. Enantioselective Angewandte Chemie (International Ed. in English). 38: 3741-3743. PMID 10649344 DOI: 10.1002/(SICI)1521-3773(19991216)38:24<3741::AID-ANIE3741>3.0.CO;2-5 |
0.333 |
|
| 2019 |
Tomooka K, Hayashi J, Uehara K, Ano Y, Kawasaki Y, Igawa K. Synthesis and Stereochemical Analysis of Dynamic Planar Chiral Nine-Membered Diallylic Amide: Significant Substituent Effect on Stereochemical Stability Heterocycles. 99: 856. DOI: 10.3987/COM-18-S(F)92 |
0.336 |
|
| 2018 |
Arae S, Furusawa M, Beppu S, Igawa K, Tomooka K, Irie R. Vinylidene -Quinone Methides: Unique Chiral Reaction Intermediates in Catalytic Asymmetric Synthesis. Chimia. 72: 892-899. PMID 30648957 DOI: 10.2533/chimia.2018.892 |
0.366 |
|
| 2018 |
Arae S, Beppu S, Kawatsu T, Igawa K, Tomooka K, Irie R. Asymmetric Synthesis of Axially Chiral Benzocarbazole Derivatives Based on Catalytic Enantioselective Hydroarylation of Alkynes. Organic Letters. PMID 30067042 DOI: 10.1021/acs.orglett.8b01945 |
0.393 |
|
| 2018 |
Arae S, Beppu S, Kawatsu T, Igawa K, Tomooka K, Irie R. Asymmetric Synthesis of Axially Chiral Benzocarbazole Derivatives Based on Catalytic Enantioselective Hydroarylation of Alkynes. Organic Letters. PMID 30067042 DOI: 10.1021/acs.orglett.8b01945 |
0.393 |
|
| 2017 |
Yoshida S, Shimizu K, Uchida K, Hazama Y, Igawa K, Tomooka K, Hosoya T. Construction of Condensed Polycyclic Aromatic Frameworks through Intramolecular Cycloaddition Reactions Involving Arynes Bearing an Internal Alkyne Moiety. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28921682 DOI: 10.1002/chem.201704345 |
0.38 |
|
| 2017 |
Igawa K, Tomooka K, Kuroo A, Yoshihiro D, Yamanaka Y. Synthesis of Stereoselectively Functionalized Silacyclopentanes Synlett. 28: 2445-2448. DOI: 10.1055/S-0036-1590826 |
0.377 |
|
| 2017 |
Igawa K, Tomooka K, Aoyama S, Kawasaki Y, Kashiwagi T, Seto Y, Ni R, Mitsuda N. Thieme Chemistry Journals Awardees: Where Are They Now? One-Pot Synthesis of Versatile Buckle Units for Click Chemistry: 4,8-Diazacyclononynes (DACNs) Synlett. 28: 2110-2114. DOI: 10.1055/S-0036-1588839 |
0.301 |
|
| 2016 |
Igawa K, Machida K, Noguchi K, Uehara K, Tomooka K. Synthesis and Stereochemical Analysis of Planar-Chiral (E)-4-[7]Orthocyclophene. The Journal of Organic Chemistry. 81: 11587-11593. PMID 27934449 DOI: 10.1021/acs.joc.6b01799 |
0.311 |
|
| 2016 |
List B, Kaib PSJ, Igawa K, Yoshihiro D, Abe Y, Tomooka K. Enantioselective Synthesis of Silacyclopentanes Synfacts. 12: 639-639. DOI: 10.1055/S-0035-1562143 |
0.497 |
|
| 2015 |
Igawa K, Ichikawa N, Ano Y, Katanoda K, Ito M, Akiyama T, Tomooka K. Catalytic Enantioselective Synthesis of Planar-Chiral Cyclic Amides Based on a Pd-Catalyzed Asymmetric Allylic Substitution Reaction. Journal of the American Chemical Society. 137: 7294-7. PMID 26053786 DOI: 10.1021/jacs.5b04340 |
0.361 |
|
| 2015 |
Ni R, Mitsuda N, Kashiwagi T, Igawa K, Tomooka K. Heteroatom-embedded medium-sized cycloalkynes: concise synthesis, structural analysis, and reactions. Angewandte Chemie (International Ed. in English). 54: 1190-4. PMID 25470001 DOI: 10.1002/anie.201409910 |
0.317 |
|
| 2015 |
Kawatsu T, Tokushima H, Takedomi Y, Imahori T, Igawa K, Tomooka K, Irie R. Synthesis, stereochemical characteristics, and coordination behavior of 2,2'-binaphthyl-1,1'-biisoquinoline as a new axially chiral bidentate ligand Arkivoc. 2015: 161-175. DOI: 10.3998/ark.5550190.p009.069 |
0.307 |
|
| 2014 |
Igawa K, Kawasaki Y, Nishino K, Mitsuda N, Tomooka K. Asymmetric ozone oxidation of silylalkenes using a C2-symmetrical dialkoxysilyl group as a chiral auxiliary. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 9255-8. PMID 24939819 DOI: 10.1002/chem.201402996 |
0.352 |
|
| 2014 |
Tomooka K, Miyasaka S, Motomura S, Igawa K. Planar chiral dialkoxysilane: introduction of inherent chirality and high reactivity in conventional achiral alkene. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 7598-602. PMID 24802258 DOI: 10.1002/chem.201402434 |
0.33 |
|
| 2014 |
Igawa K, Kawasaki Y, Nishino K, Mitsuda N, Tomooka K. Asymmetric ozone oxidation of silylalkenes using a C2- symmetrical dialkoxysilyl group as a chiral auxiliary Chemistry - a European Journal. 20: 9255-9258. DOI: 10.1002/chem.201402996 |
0.339 |
|
| 2014 |
Tomooka K, Miyasaka S, Motomura S, Igawa K. Planar chiral dialkoxysilane: Introduction of inherent chirality and high reactivity in conventional achiral alkene Chemistry - a European Journal. 20: 7598-7602. DOI: 10.1002/chem.201402434 |
0.315 |
|
| 2013 |
Igawa K, Kawabata T, Ni R, Tomooka K. Synthesis, structural analysis, and reaction of 3-Aza-5-[7]orthocyclophyne Chemistry Letters. 42: 1374-1376. DOI: 10.1246/cl.130735 |
0.359 |
|
| 2012 |
Igawa K, Yoshihiro D, Ichikawa N, Kokan N, Tomooka K. Catalytic enantioselective synthesis of alkenylhydrosilanes. Angewandte Chemie (International Ed. in English). 51: 12745-8. PMID 23136024 DOI: 10.1002/anie.201207361 |
0.44 |
|
| 2012 |
Igawa K, Yoshihiro D, Ichikawa N, Kokan N, Tomooka K. Catalytic enantioselective synthesis of alkenylhydrosilanes Angewandte Chemie - International Edition. 51: 12745-12748. DOI: 10.1002/anie.201207361 |
0.389 |
|
| 2011 |
Tomooka K, Suzuki M, Shimada M, Ni R, Uehara K. Stereoselective multimodal transformations of planar chiral 9-membered diallylic amides. Organic Letters. 13: 4926-9. PMID 21861490 DOI: 10.1021/ol2025873 |
0.326 |
|
| 2011 |
Tomooka K, Inoue H, Igawa K. Synthesis and stereochemical behavior of (E)-cyclononene derivatives Chemistry Letters. 40: 591-593. DOI: 10.1246/cl.2011.591 |
0.302 |
|
| 2011 |
Irie R, Tanoue A, Urakawa S, Imahori T, Igawa K, Matsumoto T, Tomooka K, Kikuta S, Uchida T, Katsuki T. Synthesis and stereochemical behavior of a new chiral oxa[7]heterohelicene Chemistry Letters. 40: 1343-1345. DOI: 10.1246/cl.2011.1343 |
0.316 |
|
| 2010 |
Tomooka K, Uehara K, Nishikawa R, Suzuki M, Igawa K. Enantioselective synthesis of planar chiral organonitrogen cycles. Journal of the American Chemical Society. 132: 9232-3. PMID 20565091 DOI: 10.1021/ja1024657 |
0.396 |
|
| 2010 |
Igawa K, Kokan N, Tomooka K. Asymmetrie synthesis of chiral silacarboxylic acids and their ester derivatives Angewandte Chemie - International Edition. 49: 728-731. PMID 20029860 DOI: 10.1002/anie.200904922 |
0.367 |
|
| 2010 |
Tomooka K, Uehara K, Nishikawa R, Suzuki M, Igawa K. Enantioselective synthesis of planar chiral organonitrogen cycles Journal of the American Chemical Society. 132: 9232-9233. DOI: 10.1021/ja1024657 |
0.37 |
|
| 2010 |
Tomoyasu T, Tomooka K, Nakai T. ChemInform Abstract: Generation and Asymmetric Michael Addition Reaction of Chirally N-Protected α-Aminoalkyl Cyanocuprates. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200021071 |
0.308 |
|
| 2010 |
Tomooka K, Nakazaki A, Nakai T. ChemInform Abstract: A Novel Aryl Migration from Silicon to Carbon: An Efficient Approach to Asymmetric Synthesis of α-Aryl β-Hydroxy Cyclic Amines and Silanols. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200015033 |
0.376 |
|
| 2010 |
Tomooka K, Wang L, Komine N, Nakai T. ChemInform Abstract: Enantioselective Reactions of α-Methoxybenzyllithium Generated by t-BuLi/Chiral Bis(oxazoline) Complex with Aldehydes. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199947050 |
0.3 |
|
| 2010 |
Tomooka K, Igarashi T, Kishi N, Nakai T. ChemInform Abstract: Olefinic Stereoselection in the [2,3]-Wittig Rearrangement of α,β-Disubstituted Allylic Ethers Forming Trisubstituted Olefins. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199945200 |
0.311 |
|
| 2010 |
Tomooka K, Komine N, Sasaki T, Shimizu H, Nakai T. ChemInform Abstract: Enantioselective Carbanion Cyclization of 5-Alkenyl Carbamates Induced by Asymmetric Lithiation with s-Butyllithium/(-)-Sparteine System. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199910083 |
0.308 |
|
| 2010 |
TOMOYASU T, TOMOOKA K, NAKAI T. ChemInform Abstract: A New Approach to Asymmetric Synthesis of β-Amino Alcohols by Means of α-Chirally Protected Amino Alkyllithiums. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199904070 |
0.365 |
|
| 2010 |
NAKAI T, TOMOOKA K. ChemInform Abstract: Asymmetric (2,3)-Wittig Rearrangement as a General Tool for Asymmetric Synthesis Cheminform. 28: no-no. DOI: 10.1002/CHIN.199728253 |
0.409 |
|
| 2010 |
TOMOOKA K, NAGASAWA A, WEI S, NAKAI T. ChemInform Abstract: Chiral Dienolate Chemistry in Remote Asymmetric Induction: The Asymmetric Aldol/Oxy-Cope Strategy for Asymmetric Synthesis of γ, δ-Dichiral α,β-Unsaturated Acid Derivatives. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199716039 |
0.412 |
|
| 2010 |
TOMOOKA K, NAGASAWA A, WEI S, NAKAI T. ChemInform Abstract: Chiral Dienolate Chemistry in Remote Asymmetric Induction: The Allylation/Cope Rearrangement Sequence Leading to γ-Chiral . alpha.,β-Unsaturated Acid Derivatives. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199716038 |
0.321 |
|
| 2010 |
TOMOOKA K, ISHIKAWA K, NAKAI T. ChemInform Abstract: Asymmetric (2,3)-Wittig Rearrangement Approach to the Formal Synthesis of (+)-Brefeldin A. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199603253 |
0.398 |
|
| 2010 |
TOMOOKA K, KEONG P, NAKAI T. ChemInform Abstract: 1,4-Remote Stereocontrol via Asymmetric (2,3)-Wittig Rearrangements. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199532055 |
0.325 |
|
| 2010 |
NAKAZAWA M, SAKAMOTO Y, TAKAHASHI T, TOMOOKA K, ISHIKAWA K, NAKAI T. ChemInform Abstract: A New Approach to Asymmetric Synthesis of Stork′s Prostaglandin Intermediate. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199404075 |
0.389 |
|
| 2010 |
WEI S, TOMOOKA K, NAKAI T. ChemInform Abstract: Acyclic Diastereocontrol and Asymmetric Transmission via Anionic Oxy- Cope Rearrangement. Synthesis of Key Precursors of (+)-Faranal and (-)- Antirhine. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199324086 |
0.44 |
|
| 2009 |
Tomooka K, Igawa K, Takada J, Shimono T. Synthesis of Chiral Silanols from Desymmetrization of Dialkoxysilanes Synfacts. 2009: 0296-0296. DOI: 10.1055/S-0028-1087758 |
0.455 |
|
| 2008 |
Igawa K, Takada J, Shimono T, Tomooka K. Enantioselective synthesis of silanol. Journal of the American Chemical Society. 130: 16132-3. PMID 18998686 DOI: 10.1021/ja805848z |
0.339 |
|
| 2008 |
Tomooka K, Nakazaki A, Usuki J. Stereoselective 1,4-Phenyl
Migration from Silicon to Carbon in α-Siloxy Cyclic Acetal
Systems: A Concise Synthesis of 1,2-cis-Phenyl C-Glycoside and Enantioenriched
Silanol Synlett. 2008: 2064-2068. DOI: 10.1055/S-2008-1077953 |
0.313 |
|
| 2008 |
Igawa K, Sakita K, Murakami M, Tomooka K. Partial oxidation of alkenylsilanes with ozone: A novel stereoselective approach to the diol and triol derivatives Synthesis. 1641-1645. DOI: 10.1055/s-2008-1032161 |
0.351 |
|
| 2008 |
Tomooka K, Sakamaki J, Harada M, Wada R. Enantioselective [1,2]-Stevens Rearrangement Using Sugar-Derived Alkoxides as Chiral Promoters Synlett. 2008: 683-686. DOI: 10.1055/S-2008-1032107 |
0.35 |
|
| 2008 |
Igawa K, Takada J, Shimono T, Tomooka K. Enantioselective synthesis of silanol Journal of the American Chemical Society. 130: 16132-16133. DOI: 10.1021/ja805848z |
0.315 |
|
| 2008 |
Tomooka K, Akiyama T, Man P, Suzuki M. Asymmetric synthesis of (−)- and (+)-kainic acid using a planar chiral amide as a chiral building block Tetrahedron Letters. 49: 6327-6329. DOI: 10.1016/J.TETLET.2008.08.058 |
0.378 |
|
| 2006 |
Murakami M, Sakita K, Igawa K, Tomooka K. Stereoselective oxy-functionalization of gamma-silyl allylic alcohols with ozone: a facile synthesis of silyl peroxide and its reactions. Organic Letters. 8: 4023-6. PMID 16928064 DOI: 10.1021/ol061635r |
0.308 |
|
| 2006 |
Tomooka K, Suzuki M, Shimada M, Yanagitsuru S, Uehara K. Planar chiral cyclic amine and its derivatives: synthesis and stereochemical behavior. Organic Letters. 8: 963-5. PMID 16494485 DOI: 10.1021/ol053141k |
0.375 |
|
| 2006 |
Murakami M, Sakita K, Igawa K, Tomooka K. Stereoselective oxy-functionalization of γ-silyl allylic alcohols with ozone: A facile synthesis of silyl peroxide and its reactions Organic Letters. 8: 4023-4026. DOI: 10.1021/ol061635r |
0.334 |
|
| 2005 |
Tomooka K, Komine N, Fujiki D, Nakai T, Yanagitsuru S. Planar chiral cyclic ether: asymmetric resolution and chirality transformation. Journal of the American Chemical Society. 127: 12182-3. PMID 16131170 DOI: 10.1021/Ja053347G |
0.353 |
|
| 2005 |
Tomooka K, Komine N, Fujiki D, Nakai T, Yanagitsuru S. Planar Chiral Cyclic Ether Synfacts. 2005: 303-303. DOI: 10.1055/S-2005-921611 |
0.331 |
|
| 2004 |
Tomooka K, Komine N, Nakai T. External chiral ligand-induced enantioselective versions of the [2,3]-Wittig sigmatropic rearrangement. Chirality. 12: 505-9. PMID 10824178 DOI: 10.1002/(SICI)1520-636X(2000)12:5/6<505::AID-CHIR36>3.0.CO;2-3 |
0.302 |
|
| 2004 |
Harada M, Nakai T, Tomooka K. Stevens rearrangement of a cyclic hemiacetal system: Diastereoselective approach to chiral α-amino ketone Synlett. 2004: 365-367. DOI: 10.1055/S-2003-44998 |
0.341 |
|
| 2003 |
Tomoyasu T, Tomooka K, Nakai T. Asymmetric synthesis of enantio-enriched acyclic α-amino alkylstannanes and rearrangement behavior of carbanions thereof Tetrahedron Letters. 44: 1239-1242. DOI: 10.1016/S0040-4039(02)02811-3 |
0.333 |
|
| 2003 |
Tomoyasu T, Tomooka K, Nakai T. Asymmetric Synthesis of Enantio-Enriched Acyclic α-Amino Alkylstannanes and Rearrangement Behavior of Carbanions Thereof. Cheminform. 34. DOI: 10.1002/CHIN.200317152 |
0.333 |
|
| 2001 |
Tomooka K, Kikuchi M, Igawa K, Suzuki M, Keong P, Nakai T. ChemInform Abstract: Stereoselective Total Synthesis of Zaragozic Acid A Based on an Acetal [1,2] Wittig Rearrangement. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200115239 |
0.367 |
|
| 2001 |
Tomooka K, Yamamoto H, Nakai T. ChemInform Abstract: Stereoselective Synthesis of Highly Functionalized C-Glycosides Based on Acetal [1,2] and [1,4] Wittig Rearrangements. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200115206 |
0.395 |
|
| 2000 |
Tomooka K, Kikuchi M, Igawa K, Suzuki M, Keong PH, Nakai T. Stereoselective Total Synthesis of Zaragozic Acid A based on an Acetal Angewandte Chemie (International Ed. in English). 39: 4502-4505. PMID 11169650 DOI: 10.1002/1521-3773(20001215)39:24<4502::Aid-Anie4502>3.0.Co;2-K |
0.322 |
|
| 2000 |
Tomooka K, Yamamoto H, Nakai T. Stereoselective Synthesis of Highly Functionalized C-Glycosides based on Acetal Angewandte Chemie (International Ed. in English). 39: 4500-4502. PMID 11169649 DOI: 10.1002/1521-3773(20001215)39:24<4500::Aid-Anie4500>3.3.Co;2-N |
0.353 |
|
| 2000 |
Tomooka K, Kikuchi M, Igawa K, Suzuki M, Keong P, Nakai T. Stereoselective Total Synthesis of Zaragozic Acid A based on an Acetal [1,2] Wittig Rearrangement Angewandte Chemie. 112: 4676-4679. DOI: 10.1002/1521-3757(20001215)112:24<4676::AID-ANGE4676>3.0.CO;2-N |
0.341 |
|
| 1999 |
Tomooka K, Nakazaki A, Nakai T. A Novel Aryl Migration from Silicon to Carbon: An Efficient Approach to Asymmetric Synthesis of α-Aryl β-Hydroxy Cyclic Amines and Silanols Journal of the American Chemical Society. 122: 408-409. DOI: 10.1021/JA993295T |
0.364 |
|
| 1998 |
Tomoyasu T, Tomooka K, Nakai T. A New Approach to Asymmetric Synthesis of β-Amino Alcohols by Means of α-Chirally Protected Amino Alkyllithiums Synlett. 1998: 1147-1149. DOI: 10.1055/S-1998-1891 |
0.354 |
|
| 1997 |
Nakai T, Tomooka K. Asymmetric (2,3)-Wittig rearrangement as a general tool for asymmetric synthesis Pure and Applied Chemistry. 69: 595-600. DOI: 10.1351/Pac199769030595 |
0.427 |
|
| 1997 |
Wender PA, Badham NF, Conway SP, Floreancig PE, Glass TE, Granicher C, Houze JB, Janichen J, Lee D, Marquess DG, McGrane PL, Meng W, Mucciaro TP, Muhlebach M, Natchus MG, ... ... Tomooka K, et al. The pinene path tot taxanes. 5. Stereocontrolled synthesis of a versatile taxane precursor Journal of the American Chemical Society. 119: 2755-2756. DOI: 10.1021/Ja9635387 |
0.584 |
|
| 1997 |
Tomooka K, Komine N, Nakai T. Cyclization of enantio-enriched α-(homoallyloxy)alkyllithiums: Evidence for retention of configuration at the carbanion center Tetrahedron Letters. 38: 8939-8942. DOI: 10.1016/S0040-4039(97)10327-6 |
0.31 |
|
| 1996 |
Tomooka K, Nakai T. [1, 2] -Wittig Rearrangement Stereochemical Features and Synthetic Utilities Journal of Synthetic Organic Chemistry Japan. 54: 1000-1008. DOI: 10.5059/Yukigoseikyokaishi.54.1000 |
0.355 |
|
| 1996 |
Tomooka K, Nagasawa A, Wei SY, Nakai T. Chiral dienolate chemistry in remote asymmetric induction: The asymmetric aldol / oxycope strategy for asymmetric synthesis of γ,δ-dichiral α, β-unsaturated acid derivatives Tetrahedron Letters. 37: 8899-8900. DOI: 10.1016/S0040-4039(96)02078-3 |
0.335 |
|
| 1996 |
Tomooka K, Nagasawa A, Wei S, Nakai T. Chiral dienolate chemistry in remote asymmetric induction: the allylation / cope rearrangement sequence leading to γ-chiral α, β-unsaturated acid derivatives Tetrahedron Letters. 37: 8895-8898. DOI: 10.1016/S0040-4039(96)02077-1 |
0.385 |
|
| 1995 |
Tomooka K, Ishikawa K, Nakai T. Asymmetric [2,3]-Wittig Rearrangement Approach to the Formal Synthesis of (+)-Brefeldin A Synlett. 1995: 901-902. DOI: 10.1055/S-1995-5152 |
0.375 |
|
| 1993 |
Nakazawa M, Sakamoto Y, Takahashi T, Tomooka K, Ishikawa K, Nakai T. A new approach to asymmetric synthesis of Stork's prostaglandin intermediate Tetrahedron Letters. 34: 5923-5926. DOI: 10.1016/S0040-4039(00)73815-9 |
0.351 |
|
| 1993 |
Wei SY, Tomooka K, Nakai T. Acyclic diastereocontrol and asymmetric transmission via anionic oxy-Cope rearrangement. Synthesis of key precursors of (+)-faranal and (−)-antirhine Tetrahedron. 49: 1025-1042. DOI: 10.1016/S0040-4020(01)86283-9 |
0.365 |
|
| 1992 |
Tomooka K, Matsumoto K, Suzuki K, Tsuchihashi G. An Alternative Synthetic Route to the C(11)-C(17)-Fragment of Mycinolide IV Synlett. 1992: 129-130. DOI: 10.1055/S-1992-21289 |
0.359 |
|
| 1989 |
Nakata M, Arai M, Tomooka K, Ohsawa N, Kinoshita M. Total Synthesis of Erythronolide A Bulletin of the Chemical Society of Japan. 62: 2618-2635. DOI: 10.1246/Bcsj.62.2618 |
0.373 |
|
| 1989 |
Tomooka K, Okinaga T, Suzuki K, Tsuchihashi G. Lactols in stereoselection 3 Tetrahedron Letters. 30: 1563-1566. DOI: 10.1016/S0040-4039(00)99520-0 |
0.528 |
|
| 1989 |
NAKATA M, ARAI M, TOMOOKA K, OHSAWA N, KINOSHITA M. ChemInform Abstract: Synthetic Studies of Erythromycins. Part 4. Total Synthesis of Erythronolide A. Cheminform. 20. DOI: 10.1002/CHIN.198951304 |
0.457 |
|
| 1987 |
Suzuki K, Matsumoto T, Tomooka K, Matsumoto K, Tsuchihashi G. Stereocontrolled First Total Synthesis of Mycinolide IV Chemistry Letters. 16: 113-116. DOI: 10.1246/Cl.1987.113 |
0.582 |
|
| 1987 |
Tomooka K, Matsuzawa K, Suzuki K, Tsuchihashi G. Lactols in stereoselection 2. Stereoselective synthesis of disubstituted cyclic ethers. Tetrahedron Letters. 28: 6339-6342. DOI: 10.1016/S0040-4039(01)91368-1 |
0.56 |
|
| 1987 |
Tomooka K, Okinaga T, Suzuki K, Tsuchihashi G. Lactols in stereoselection 1. Highly selective 1,4- and 1,5-asymmetric induction Tetrahedron Letters. 28: 6335-6338. DOI: 10.1016/S0040-4039(01)91367-X |
0.565 |
|
| 1987 |
SUZUKI K, MATSUMOTO T, TOMOOKA K, MATSUMOTO K, TSUCHIHASHI G. ChemInform Abstract: Stereocontrolled First Total Synthesis of Mycinolide IV (I). Cheminform. 18. DOI: 10.1002/CHIN.198737332 |
0.456 |
|
| 1986 |
Suzuki K, Tomooka K, Katayama E, Matsumoto T, Tsuchihashi G. Stereocontrolled asymmetric total synthesis of protomycinolide IV Journal of the American Chemical Society. 108: 5221-5229. DOI: 10.1021/Ja00277A028 |
0.569 |
|
| 1986 |
Kinoshita M, Arai M, Tomooka K, Nakata M. Synthetic studies of erythromycins. II. Enantiospecific synthesis of A C-10-C-13 segment of erythronolide a from D-ribose Tetrahedron Letters. 27: 1811-1814. DOI: 10.1016/S0040-4039(00)84382-8 |
0.337 |
|
| 1986 |
SUZUKI K, TOMOOKA K, KATAYAMA E, MATSUMOTO T, TSUCHIHASHI G. ChemInform Abstract: Stereocontrolled Asymmetric Total Synthesis of Protomycinolide IV (XIII). Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198652321 |
0.472 |
|
| 1986 |
KINOSHITA M, ARAI M, TOMOOKA K, NAKATA M, OHSAWA N. ChemInform Abstract: Synthetic Studies of Erythromycins. Part 2. Enantiospecific Synthesis of a C-10-C-13 Segment of Erythronolide A from D-Ribose. Synthetic Studies of Erythromycins. Part 3. Total Synthesis of Erythronolide A Through (9S)-9-Dihydroerythr Chemischer Informationsdienst. 17. DOI: 10.1002/CHIN.198636330 |
0.331 |
|
| 1985 |
Suzuki K, Tomooka K, Shimazaki M, Tsuchihashi G. Conformational effects in organoaluminum-promoted pinacol-type rearrangement Tetrahedron Letters. 26: 4781-4784. DOI: 10.1016/S0040-4039(00)94950-5 |
0.483 |
|
| 1985 |
Suzuki K, Tomooka K, Matsumoto T, Katayama E, Tsuchihashi G. Stereoselective synthesis of C(1)–C(9) and C(11)–C(17)fragments of protomycinolide iv based on asymmetric pinacol-typerearrangement Tetrahedron Letters. 26: 3711-3714. DOI: 10.1016/S0040-4039(00)89230-8 |
0.512 |
|
| 1985 |
Suzuki K, Katayama E, Tomooka K, Matsumoto T, Tsuchihashi G. Highly stereoselective approach to chiral building block possessing three contiguous asymmetric centers. Preparation of four possible diastereomers of β,β′-dimethyl-bis-homoallylic alcohol derivative Tetrahedron Letters. 26: 3707-3710. DOI: 10.1016/S0040-4039(00)89229-1 |
0.553 |
|
| 1985 |
SUZUKI K, KATAYAMA E, TOMOOKA K, MATSUMOTO T, TSUCHIHASHI G. ChemInform Abstract: Highly Stereoselective Approach to Chiral Building Block Possessing Three Contiguous Asymmetric Centers. Three Continuous Asymmetric Centers. Preparation of Four Possible Diastereomers of β,β′-Di-methyl-bis-homoallylic Alcohol Derivat Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198552093 |
0.505 |
|
| 1985 |
TSUCHIHASHI G, TOMOOKA K, SUZUKI K. ChemInform Abstract: COMPLETELY STEREOSPECIFIC 1,2-MIGRATION OF ALKYL GROUPS IN DIETHYLALUMINUM CHLORIDE (ET2ALCL) PROMOTED PINACOL-TYPE REARRANGEMENT Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198504140 |
0.449 |
|
| 1984 |
Tsuchihashi G, Tomooka K, Suzuki K. Completely stereospecific 1,2-migration of alkyl groups in Et2AlCl promoted pinacol-type rearrangement Tetrahedron Letters. 25: 4253-4256. DOI: 10.1016/S0040-4039(01)81409-X |
0.537 |
|
| Show low-probability matches. |