| Year |
Citation |
Score |
| 2010 |
Takai K, Heathcock CH. Generation of novel nucleophilic organometallic species and their applications to organic synthesis Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. 68: 3-18. DOI: 10.5059/Yukigoseikyokaishi.68.3 |
0.4 |
|
| 2010 |
HEATHCOCK CH, BROWN RCD, NORMAN TC. ChemInform Abstract: Synthesis of Petrosins C (I) and D (II). Cheminform. 29: no-no. DOI: 10.1002/chin.199849271 |
0.654 |
|
| 2010 |
WALKER MA, HEATHCOCK CH. ChemInform Abstract: Acyclic Stereoselection. Part 54. Extending the Scope of the Evans Asymmetric Aldol Reaction: Preparation of anti- and “Non-Evans” syn- Aldols. Cheminform. 23: no-no. DOI: 10.1002/chin.199208067 |
0.328 |
|
| 2010 |
OARE DA, HEATHCOCK CH. ChemInform Abstract: Acyclic Stereocontrol in Michael Addition Reactions of Enamines and Enol Ethers Cheminform. 22: no-no. DOI: 10.1002/chin.199132288 |
0.785 |
|
| 2007 |
Oare DA, Heathcock CH. Acyclic stereocontrol in Michael addition reactions of enamines and enol ethers Topics in Stereochemistry. 20: 87-170. DOI: 10.1002/9780470147290.Ch2 |
0.793 |
|
| 2007 |
Oare DA, Heathcock CH. Stereochemistry of the Base‐Promoted Michael Addition Reaction Topics in Stereochemistry. 19: 227-407. DOI: 10.1002/9780470147283.Ch5 |
0.779 |
|
| 2004 |
Christie HS, Heathcock CH. Total synthesis of (+/-)-halichlorine, (+/-)-pinnaic acid, and (+/-)-tauropinnaic acid. Proceedings of the National Academy of Sciences of the United States of America. 101: 12079-84. PMID 15299146 DOI: 10.1073/Pnas.0403887101 |
0.449 |
|
| 2004 |
Brito-Arias M, Pereda-Miranda R, Heathcock CH. Synthesis of tricolorin F. The Journal of Organic Chemistry. 69: 4567-70. PMID 15230576 DOI: 10.1021/Jo030244C |
0.382 |
|
| 2003 |
Heathcock CH, McLaughlin M, Medina J, Hubbs JL, Wallace GA, Scott R, Claffey MM, Hayes CJ, Ott GR. Multigram synthesis of the C29-C51 subunit and completion of the total synthesis of altohyrtin C (spongistatin 2). Journal of the American Chemical Society. 125: 12844-9. PMID 14558833 DOI: 10.1021/Ja030317+ |
0.791 |
|
| 2003 |
Hubbs JL, Heathcock CH. A second-generation synthesis of the C1-C28 portion of the altohyrtins (spongistatins). Journal of the American Chemical Society. 125: 12836-43. PMID 14558832 DOI: 10.1021/Ja030316H |
0.719 |
|
| 2003 |
Young SD, Buse CT, Heathcock CH. 2‐Methyl‐2‐(Trimethylsiloxy)Pentan‐3‐one Organic Syntheses. 79-79. DOI: 10.1002/0471264180.Os063.09 |
0.38 |
|
| 2003 |
Heathcock CH, Hassner A. Methyl (trans‐2‐Iodo‐1‐Tetralin)Carbamate Organic Syntheses. 112-112. DOI: 10.1002/0471264180.Os051.28 |
0.333 |
|
| 2003 |
Heathcock CH, Hassner A. Aziridines from β-Iodocarbamates: 1,2,3,4-Tetrahydronaphthalene(1,2)imine Organic Syntheses. 53-53. DOI: 10.1002/0471264180.Os051.12 |
0.309 |
|
| 2002 |
Skyler D, Heathcock CH. The pyridoacridine family tree: a useful scheme for designing synthesis and predicting undiscovered natural products. Journal of Natural Products. 65: 1573-81. PMID 12444679 DOI: 10.1021/Np020016Y |
0.76 |
|
| 2002 |
Fell JD, Heathcock CH. Oxidative fragmentation of pregna-14,16-dien-20-ones to 14 beta-hydroxyandrost-15-en-17-ones. The Journal of Organic Chemistry. 67: 4742-6. PMID 12098283 DOI: 10.1021/Jo011175+ |
0.805 |
|
| 2002 |
Blazey CM, Heathcock CH. Regiochemistry in 1,3-dipolar cycloadditions of the azomethine ylide formed from diethyl aminomalonate and paraformaldehyde. The Journal of Organic Chemistry. 67: 298-300. PMID 11777476 DOI: 10.1021/Jo010645X |
0.804 |
|
| 2002 |
Kedrowski BL, Heathcock CH. Thiazoline ring formation from 2-methylcysteines and 2-halomethylalanines Heterocycles. 58: 601-634. DOI: 10.3987/Com-02-S(M)60 |
0.789 |
|
| 2001 |
Skyler D, Heathcock CH. A simple biomimetic synthesis of styelsamine B. Organic Letters. 3: 4323-4. PMID 11784208 DOI: 10.1021/Ol010262L |
0.803 |
|
| 2001 |
Hinman MM, Heathcock CH. A synthetic approach to the Stemona alkaloids. The Journal of Organic Chemistry. 66: 7751-6. PMID 11701032 DOI: 10.1021/Jo0106391 |
0.356 |
|
| 2001 |
Wallace GA, Heathcock CH. Further studies of the Daphniphyllum alkaloid polycyclization cascade. The Journal of Organic Chemistry. 66: 450-4. PMID 11429813 DOI: 10.1021/Jo001145R |
0.731 |
|
| 2000 |
Yamamoto K, Heathcock CH. alpha,beta-epoxy vinyl triflates in Pd-catalyzed reactions. Organic Letters. 2: 1709-12. PMID 10880207 DOI: 10.1021/Ol000064E |
0.572 |
|
| 2000 |
Wallace GA, Scott RW, Heathcock CH. Synthesis of the C29-C44 portion of spongistatin 1 (altohyrtin A). The Journal of Organic Chemistry. 65: 4145-52. PMID 10866633 DOI: 10.1021/jo0002801 |
0.672 |
|
| 2000 |
Toczko MA, Heathcock CH. Total synthesis of (+/-)-aspidospermidine. The Journal of Organic Chemistry. 65: 2642-5. PMID 10808435 DOI: 10.1021/Jo991599S |
0.826 |
|
| 1999 |
Claffey MM, Hayes CJ, Heathcock CH. Synthesis of the C1-C28 Portion of Spongistatin 1 (Altohyrtin A). The Journal of Organic Chemistry. 64: 8267-8274. PMID 11674747 DOI: 10.1021/Jo9910987 |
0.38 |
|
| 1999 |
Liu JF, Heathcock CH. Total Synthesis of (+/-)-Cylindricines A and B. The Journal of Organic Chemistry. 64: 8263-8266. PMID 11674746 DOI: 10.1021/Jo991020Q |
0.401 |
|
| 1999 |
Mapp AK, Heathcock CH. Total Synthesis of Myxalamide A. The Journal of Organic Chemistry. 64: 23-27. PMID 11674080 DOI: 10.1021/Jo9813742 |
0.698 |
|
| 1999 |
Aubart KM, Heathcock CH. A Biomimetic Approach to the Discorhabdin Alkaloids: Total Syntheses of Discorhabdins C and E and Dethiadiscorhabdin D. The Journal of Organic Chemistry. 64: 16-22. PMID 11674079 DOI: 10.1021/Jo9815397 |
0.365 |
|
| 1999 |
Hubbs JL, Heathcock CH. Total synthesis of (+/-)-isoschizogamine. Organic Letters. 1: 1315-7. PMID 10825981 DOI: 10.1021/Ol9902632 |
0.743 |
|
| 1999 |
Chi S, Heathcock CH. Total syntheses of (+/-)-preussomerins G and I. Organic Letters. 1: 3-5. PMID 10822527 DOI: 10.1021/Ol990020+ |
0.387 |
|
| 1998 |
Denhart DJ, Griffith DA, Heathcock CH. Synthesis of the tricyclic core of sarain A. Use of formaldehyde in an intramolecular Grigg azomethine ylide cyclization Journal of Organic Chemistry. 63: 9616-9617. DOI: 10.1021/Jo981801B |
0.669 |
|
| 1998 |
Scott RW, Epperson J, Heathcock CH. Total Synthesis of Petrosin, Petrosin A, and Petrosin B Journal of Organic Chemistry. 63: 5001-5012. DOI: 10.1021/Jo9801768 |
0.411 |
|
| 1997 |
Larson DP, Heathcock CH. Total Synthesis of Tricolorin A. The Journal of Organic Chemistry. 62: 8406-8418. PMID 11671979 DOI: 10.1021/jo971413u |
0.321 |
|
| 1997 |
Szczepankiewicz BG, Heathcock CH. A novel method for suppression of the abnormal Fischer indole synthesis Tetrahedron. 53: 8853-8870. DOI: 10.1016/S0040-4020(97)90396-3 |
0.379 |
|
| 1996 |
McDermott TS, Mortlock AA, Heathcock CH. Total Syntheses of (-)-Papuamine and (-)-Haliclonadiamine. The Journal of Organic Chemistry. 61: 700-709. PMID 11666993 DOI: 10.1021/Jo951647I |
0.406 |
|
| 1996 |
Heathcock CH. Nature knows best: an amazing reaction cascade is uncovered by design and discovery. Proceedings of the National Academy of Sciences of the United States of America. 93: 14323-7. PMID 8962049 DOI: 10.1073/Pnas.93.25.14323 |
0.371 |
|
| 1996 |
Scott RW, Heathcock CH. An efficient synthesis of 3,4,6-tri-O-benzyl-2-C-methyl-D-glucal. Carbohydrate Research. 291: 205-8. PMID 8864231 DOI: 10.1016/S0008-6215(96)00162-0 |
0.342 |
|
| 1996 |
Parsons RL, Heathcock CH. Total Synthesis of (-)-Tantazole B Synlett. 1996: 1168-1170. DOI: 10.1055/S-1996-5716 |
0.328 |
|
| 1996 |
Marshall KA, Mapp AK, Heathcock CH. Synthesis of a 2,7-dioxatricyclo[4.2.1.03,8]nonane: A model study for possible application in a synthesis of dictyoxetane Journal of Organic Chemistry. 61: 9135-9145. DOI: 10.1021/Jo961680K |
0.676 |
|
| 1996 |
Caron S, Stoermer D, Mapp AK, Heathcock CH. Total synthesis of zaragozic acid A (squalestatin S1). Synthesis of the relay compound Journal of Organic Chemistry. 61: 9126-9134. DOI: 10.1021/Jo961534E |
0.688 |
|
| 1996 |
Stoermer D, Caron S, Heathcock CH. Total synthesis of zaragozic acid A (squalestatin S1). Degradation to a relay compound and reassembly of the natural product Journal of Organic Chemistry. 61: 9115-9125. DOI: 10.1021/Jo961533M |
0.395 |
|
| 1996 |
Larson DP, Heathcock CH. Synthesis of the macrolactone disaccharide subunit of tricolorin A Journal of Organic Chemistry. 61: 5208-5209. DOI: 10.1021/Jo960655B |
0.376 |
|
| 1996 |
Brimble MA, Heathcock CH, Nobin GN. Synthesis and ene reactions of di-(-)-methyl diazenedicarboxylate Tetrahedron Asymmetry. 7: 2007-2016. DOI: 10.1016/0957-4166(96)00242-X |
0.487 |
|
| 1996 |
Caron S, McDonald AI, Heathcock CH. An improved synthesis of 1,6-anhydro-2,3-di-O-benzyl-β-D-xylo-hexopyranos-4-ulose Carbohydrate Research. 281: 179-182. DOI: 10.1016/0008-6215(95)00335-5 |
0.303 |
|
| 1995 |
Heathcock CH, Clasby M, Griffith DA, Henke BR, Sharp MJ. Progress toward the Synthesis of Sarain A Synlett. 1995: 467-474. DOI: 10.1055/S-1995-5298 |
0.659 |
|
| 1995 |
Raimundo BC, Heathcock CH. Further Studies on the Anti-Selective Aldol Reaction of Chiral Imides Synlett. 1995: 1213-1214. DOI: 10.1055/S-1995-5246 |
0.366 |
|
| 1995 |
Caron S, McDonald AI, Heathcock CH. Synthesis of 1-substituted and 1,4-disubstituted 2,3-di-O-benzyl-1,6-anhydrogalactofuranoses Journal of Organic Chemistry. 60: 2780-2785. DOI: 10.1021/Jo00114A028 |
0.356 |
|
| 1995 |
Heathcock CH, Kath JC, Ruggeri RB. Daphniphyllum alkaloids. 16. Total synthesis of (+)-codaphniphylline Journal of Organic Chemistry. 60: 1120-1130. DOI: 10.1021/Jo00110A013 |
0.424 |
|
| 1995 |
Griffith DA, Heathcock CH. Progress toward the synthesis of sarain A: An unanticipated rearrangement Tetrahedron Letters. 36: 2381-2384. DOI: 10.1016/0040-4039(95)00283-I |
0.67 |
|
| 1994 |
Heathcock CH, Smith SC. Synthesis and biological activity of unsymmetrical bis-steroidal pyrazines related to the cytotoxic marine natural product cephalostatin 1 Journal of Organic Chemistry. 59: 6828-6839. DOI: 10.1021/Jo00101A052 |
0.338 |
|
| 1994 |
Szczepankiewicz BG, Heathcock CH. Total synthesis of diplamine, a cytotoxic pyridoacridine alkaloid from a Pacific tunicate Journal of Organic Chemistry. 59: 3512-3513. DOI: 10.1021/Jo00092A002 |
0.395 |
|
| 1994 |
Scott RW, Epperson JR, Heathcock CH. Total Synthesis of Petrosin Journal of the American Chemical Society. 116: 8853-8854. DOI: 10.1021/Ja00098A073 |
0.417 |
|
| 1994 |
Parsons RL, Heathcock CH. Total synthesis of mirabazole B Tetrahedron Letters. 35: 1383-1384. DOI: 10.1016/S0040-4039(00)76224-1 |
0.328 |
|
| 1994 |
Parsons RL, Heathcock CH. Revision of the stereostructure of mirabazole C Tetrahedron Letters. 35: 1379-1382. DOI: 10.1016/S0040-4039(00)76223-X |
0.316 |
|
| 1994 |
Sharp MJ, Heathcock CH. An unusual isomerization under Lawesson thiation conditions Tetrahedron Letters. 35: 3651-3652. DOI: 10.1016/S0040-4039(00)73062-0 |
0.321 |
|
| 1993 |
Ganesan A, Heathcock CH. Synthesis of unsymmetrical pyrazines by reaction of an oxadiazinone with enamines Journal of Organic Chemistry. 58: 6155-6157. DOI: 10.1021/Jo00074A058 |
0.601 |
|
| 1993 |
Clark DL, Heathcock CH. Studies on the alkylation of chiral enolates: Application toward the total synthesis of discodermolide Journal of Organic Chemistry. 58: 5878-5879. DOI: 10.1021/Jo00074A005 |
0.385 |
|
| 1993 |
Brimble MA, Heathcock CH. Allylic amination by the Lewis-acid-mediated ene reaction of diethyl azodicarboxylate with alkenes Journal of Organic Chemistry. 58: 5261-5263. DOI: 10.1021/Jo00071A042 |
0.43 |
|
| 1993 |
Stoermer D, Heathcock CH. Total synthesis of (-)-alloaristoteline, (-)-serratoline, and (+)-aristotelone Journal of Organic Chemistry. 58: 564-568. DOI: 10.1021/Jo00055A007 |
0.399 |
|
| 1993 |
Ihle NC, Heathcock CH. Palladium-catalyzed intramolecular alkyne-carbon monoxide-alkene insertion cascade for synthesis of .alpha.-methylenecyclopentenones Journal of Organic Chemistry. 58: 560-563. DOI: 10.1021/Jo00055A006 |
0.41 |
|
| 1993 |
Theisen PD, Heathcock CH. Prochiral recognition in the reaction of 3-substituted glutaric anhydrides with chiral secondary alcohols Journal of Organic Chemistry. 58: 142-146. DOI: 10.1021/Jo00053A027 |
0.361 |
|
| 1993 |
Ganosan A, Heathcock CH. A Stereochemical test of the mechanism of electrophilic substitution in 3-substituted indoles Tetrahedron Letters. 34: 439-440. DOI: 10.1016/0040-4039(93)85096-F |
0.437 |
|
| 1992 |
Henke BR, Kouklis AJ, Heathcock CH. Intramolecular 1,3-dipolar cycloaddition of stabilized azomethine ylides to unactivated dipolarophiles Journal of Organic Chemistry. 57: 7056-7066. DOI: 10.1021/Jo00052A015 |
0.316 |
|
| 1992 |
Smith SC, Heathcock CH. A convenient procedure for the synthesis of bis-steroidal pyrazines: Models for the cephalostatins Journal of Organic Chemistry. 57: 6379-6380. DOI: 10.1021/Jo00050A002 |
0.375 |
|
| 1992 |
Thompson SK, Heathcock CH. Total synthesis of some marasmane and lactarane sesquiterpenes Journal of Organic Chemistry. 57: 5979-5989. DOI: 10.1021/Jo00048A036 |
0.363 |
|
| 1992 |
Van Draanen NA, Arseniyadis S, Crimmins MT, Heathcock CH. Protocols for the preparation of each of the four possible stereoisomeric .alpha.-alkyl-.beta.-hydroxy carboxylic acids from a single chiral aldol reagent. [Erratum to document cited in CA114(17):163485y] The Journal of Organic Chemistry. 57: 5802-5802. DOI: 10.1021/Jo00047A053 |
0.342 |
|
| 1992 |
Walker MA, Heathcock CH. Total synthesis of (−)-mirabazole C Journal of Organic Chemistry. 57: 5566-5568. DOI: 10.1021/Jo00047A005 |
0.357 |
|
| 1992 |
Kerwin SM, Heathcock CH. Remote oxidation of perhydrophenanthrenes by template-directed hydrogen atom abstraction Journal of Organic Chemistry. 57: 4005-4013. DOI: 10.1021/Jo00040A050 |
0.683 |
|
| 1992 |
Heathcock CH, Ruggeri RB, McClure KF. Daphniphyllum alkaloids. 15. Total syntheses of (.+-.)-methyl homodaphniphyllate and (.+-.)-daphnilactone A The Journal of Organic Chemistry. 57: 2585-2594. DOI: 10.1021/Jo00035A012 |
0.301 |
|
| 1992 |
Heathcock CH, Stafford JA, Clark DL. Daphniphyllum alkaloids. 14. Total synthesis of (.+-.)-bukittinggine Journal of Organic Chemistry. 57: 2575-2585. DOI: 10.1021/Jo00035A011 |
0.374 |
|
| 1992 |
Heathcock CH, Piettre S, Ruggeri RB, Ragan JA, Kath JC. Daphniphyllum alkaloids. 12. A proposed biosynthesis of the pentacyclic skeleton. Proto-daphniphylline Journal of Organic Chemistry. 57: 2554-2566. DOI: 10.1021/Jo00035A009 |
0.35 |
|
| 1992 |
Heathcock CH, Hansen MM, Ruggeri RB, Kath JC. Daphniphyllum alkaloids. 11. Biomimetic total synthesis of methyl homosecodaphniphyllate. Development of the tetracyclization reaction Journal of Organic Chemistry. 57: 2544-2553. DOI: 10.1021/Jo00035A008 |
0.467 |
|
| 1992 |
Heathcock CH, Davidsen SK, Mills SG, Sanner MA. Daphniphyllum alkaloids. 10. Classical total synthesis of methyl homodaphniphyllate Journal of Organic Chemistry. 57: 2531-2544. DOI: 10.1021/Jo00035A007 |
0.442 |
|
| 1992 |
Munchhof MJ, Heathcock CH. The stereochemistry of enolate formation in THF-hexane mixtures Tetrahedron Letters. 33: 8005-8006. DOI: 10.1016/S0040-4039(00)74701-0 |
0.327 |
|
| 1992 |
Lopes RSC, Lopes CC, Heathcock CH. Synthesis of pancratistatin models Tetrahedron Letters. 33: 6775-6778. DOI: 10.1016/S0040-4039(00)61773-2 |
0.352 |
|
| 1992 |
Heathcock CH. The enchanting alkaloids of Yuzuriha Angewandte Chemie (International Edition in English). 31: 665-681. DOI: 10.1002/Anie.199206653 |
0.37 |
|
| 1992 |
Heathcock CH, Stafford JA. Daphniphyllum alkaloids. 13. Asymmetric total synthesis of (-)-secodaphniphylline Journal of Organic Chemistry. 57: 2566-2574. |
0.328 |
|
| 1991 |
Walker MA, Heathcock CH. Acyclic stereoselection. 54. Extending the scope of the Evans asymmetric aldol reaction: preparation of anti and "non-Evans" syn aldols Journal of Organic Chemistry. 56: 5747-5750. DOI: 10.1021/Jo00020A006 |
0.417 |
|
| 1991 |
Van Draanen NA, Arseniyadis S, Crimmins MT, Heathcock CH. Protocols for the preparation of each of the four possible stereoisomeric α-alkyl-β-hydroxy carboxylic acids from a single chiral aldol reagent Journal of Organic Chemistry. 56: 2499-2506. DOI: 10.1021/Jo00007A043 |
0.454 |
|
| 1990 |
Piettre S, Heathcock CH. Biomimetic total synthesis of proto-daphniphylline. Science (New York, N.Y.). 248: 1532-4. PMID 17818314 DOI: 10.1126/Science.248.4962.1532 |
0.358 |
|
| 1990 |
Montgomery SH, Pirrung MC, Heathcock CH. De novo synthesis of carbohydrates by stereoselective aldol reaction: L-cladinose. Carbohydrate Research. 202: 13-32. PMID 2224887 DOI: 10.1016/0008-6215(90)84068-6 |
0.715 |
|
| 1990 |
Heathcock CH, Piettre S, Kath J. Mechanistic investigations of a biomimetic polycyclization process that leads to the Daphniphyllum alkaloids Pure and Applied Chemistry. 62: 1911-1920. DOI: 10.1351/Pac199062101911 |
0.385 |
|
| 1990 |
Danda H, Hansen MM, Heathcock CH. Acyclic stereoselection. 48. Reversal of stereochemistry in the aldol reactions of a chiral boron enolate [Erratum to document cited in CA112(5):35733z] The Journal of Organic Chemistry. 55: 6231-6231. DOI: 10.1021/Jo00312A039 |
0.373 |
|
| 1990 |
Mori I, Ishihara K, Flippin LA, Nozaki K, Yamamoto H, Bartlett PA, Heathcock CH. Acyclic stereoselection. 52. On the mechanism of Lewis acid mediated nucleophilic substitution reactions of acetals The Journal of Organic Chemistry. 55: 6107-6115. DOI: 10.1021/Jo00312A015 |
0.553 |
|
| 1990 |
Mori I, Bartlett PA, Heathcock CH. Stereoselective additions of nucleophilic alkenes to chiral thionium ions Journal of Organic Chemistry. 55: 5966-5977. DOI: 10.1021/Jo00311A013 |
0.338 |
|
| 1990 |
Stafford JA, Heathcock CH. Daphniphyllum alkaloids. Part 8. Asymmetric total synthesis of (-)-secodaphniphylline The Journal of Organic Chemistry. 55: 5433-5434. DOI: 10.1021/Jo00307A006 |
0.495 |
|
| 1990 |
Ruggeri RB, Heathcock CH. Daphniphyllum alkaloids. Part 7. Biomimetic total synthesis of (.+-.)-methyl homodaphniphyllate The Journal of Organic Chemistry. 55: 3714-3715. DOI: 10.1021/Jo00299A006 |
0.366 |
|
| 1990 |
Thompson SK, Heathcock CH. Effect of cation, temperature, and solvent on the stereoselectivity of the Horner-Emmons reaction of trimethyl phosphonoacetate with aldehydes Journal of Organic Chemistry. 55: 3386-3388. DOI: 10.1021/Jo00297A076 |
0.363 |
|
| 1990 |
Thompson SK, Heathcock CH. Total synthesis of (.+-.)-isovelleral, a mutagenic sesquiterpene dialdehyde from Lactarius vellereus Journal of Organic Chemistry. 55: 3004-3005. DOI: 10.1021/Jo00297A009 |
0.422 |
|
| 1990 |
Mori I, Ishihara K, Heathcock CH. Acyclic stereoselection. 50. New stereoselective propanal/propanoic acid synthons for aldol reactions The Journal of Organic Chemistry. 55: 1114-1117. DOI: 10.1021/Jo00290A060 |
0.375 |
|
| 1990 |
Danda H, Hansen MM, Heathcock CH. Reversal of stereochemistry in the aldol reactions of a chiral boron enolate Journal of Organic Chemistry. 55: 173-181. DOI: 10.1021/Jo00288A029 |
0.304 |
|
| 1990 |
Oare DA, Heathcock CH. Acyclic stereoselection. 47. Stereochemistry of the Michael addition of ester and ketone enolates to .alpha.,.beta.-unsaturated ketones The Journal of Organic Chemistry. 55: 157-172. DOI: 10.1021/Jo00288A028 |
0.766 |
|
| 1990 |
Oare DA, Henderson MA, Sanner MA, Heathcock CH. Acyclic stereoselection. 46. Stereochemistry of the Michael addition of N,N-disubstituted amide and thioamide enolates to .alpha.,.beta.-unsaturated ketones The Journal of Organic Chemistry. 55: 132-157. DOI: 10.1021/Jo00288A027 |
0.746 |
|
| 1990 |
OARE DA, HEATHCOCK CH. ChemInform Abstract: Acyclic Stereoselection. Part 47. Stereochemistry of the Michael Addition of Ester and Ketone Enolates to α,β-Unsaturated Ketones. Cheminform. 21. DOI: 10.1002/chin.199027098 |
0.758 |
|
| 1990 |
Stafford JA, Heathcock CH. Asymmetric total synthesis of (-)-secodaphniphylline Journal of Organic Chemistry. 55: 5433-5434. |
0.322 |
|
| 1989 |
Heathcock CH, Davis BR, Hadley CR. Synthesis and biological evaluation of a monocyclic, fully functional analogue of compactin. Journal of Medicinal Chemistry. 32: 197-202. PMID 2909732 DOI: 10.1021/Jm00121A036 |
0.335 |
|
| 1989 |
Ruggeri RB, Heathcock CH. A proposal for biosynthesis of the Daphniphyllum alkaloids Pure and Applied Chemistry. 61: 289-292. DOI: 10.1351/Pac198961030289 |
0.355 |
|
| 1989 |
Heathcock CH, Blumenkopf TA, Smith KM. Total synthesis of (.+-.)-fawcettimine The Journal of Organic Chemistry. 54: 1548-1562. DOI: 10.1021/Jo00268A015 |
0.417 |
|
| 1989 |
Ruggeri RB, McClure KF, Heathcock CH. Daphniphyllum alkaloids. Part 5. Total synthesis of (.+-.)-daphnilactone A: a novel fragmentation reaction Journal of the American Chemical Society. 111: 1530-1531. DOI: 10.1021/Ja00186A075 |
0.459 |
|
| 1989 |
Dickman DA, Heathcock CH. Total synthesis of (.+-.)-vallesamidine Journal of the American Chemical Society. 111: 1528-1530. DOI: 10.1021/Ja00186A074 |
0.417 |
|
| 1989 |
Slough GA, Bergman RG, Heathcock CH. Synthesis of .eta.1 oxygen-bound rhodium enolates. Applications to catalytic aldol chemistry Journal of the American Chemical Society. 111: 938-949. DOI: 10.1021/Ja00185A025 |
0.348 |
|
| 1989 |
Ishihara K, Yamamoto H, Heathcock CH. Diastereoselective aldol synthesis using acetal templates Tetrahedron Letters. 30: 1825-1828. DOI: 10.1016/S0040-4039(00)99590-X |
0.445 |
|
| 1989 |
OARE DA, HEATHCOCK CH. ChemInform Abstract: Synthesis of the Cyclic Hexapeptide Echinocandin D. New Approaches to the Asymmetric Synthesis of β-Hydroxy-α-amino Acids Cheminform. 20. DOI: 10.1002/chin.198916362 |
0.767 |
|
| 1988 |
Burkhardt ER, Doney JJ, Slough GA, Stack JM, Heathcock CH, Bergman RG. Carbon-Carbon bond forming reactions of organotransition metal enolate complexes Pure and Applied Chemistry. 60: 1-6. DOI: 10.1351/Pac198860010001 |
0.318 |
|
| 1988 |
Henderson MA, Heathcock CH. Acyclic stereoselection. 44. Diastereoselectivity in the ortho ester Claisen rearrangement of chiral propargylic alcohols. Use of β-allenic esters as chiral methylmalonaldehyde synthons Journal of Organic Chemistry. 53: 4736-4745. DOI: 10.1021/Jo00255A014 |
0.35 |
|
| 1988 |
Hoagland S, Morita Y, Bai DL, Märki HP, Kees K, Brown L, Heathcock CH. Acyclic stereoselection. 43. Stereoselective synthesis of the C-8 to C-15 moiety of erythronolide A Journal of Organic Chemistry. 53: 4730-4735. DOI: 10.1021/Jo00255A013 |
0.35 |
|
| 1988 |
Norman MH, Heathcock CH. Improved synthesis of N-benzyl-5-ethyl-1,2,3,4-tetrahydropyridine Journal of Organic Chemistry. 53: 3370-3371. DOI: 10.1021/Jo00249A050 |
0.339 |
|
| 1988 |
Heathcock CH, Finkelstein BL, Jarvi ET, Radel PA, Hadley CR. Acyclic stereoselection. Part 42. 1,4- and 1,5-Stereoselection by sequential aldol addition to a .alpha.,.beta.-unsaturated aldehydes followed by Claisen rearrangement. Application to total synthesis of the vitamin E side chain and the archaebacterial C40 diol The Journal of Organic Chemistry. 53: 1922-1942. DOI: 10.1021/Jo00244A017 |
0.38 |
|
| 1988 |
Ruggeri RB, Hansen MM, Heathcock CH. Total synthesis of (.+-.)-methyl homosecodaphniphyllate. A remarkable new tetracyclization reaction Journal of the American Chemical Society. 110: 8734-8736. DOI: 10.1021/Ja00234A046 |
0.451 |
|
| 1987 |
Heathcock CH, Hadley CR, Rosen T, Theisen PD, Hecker SJ. Total synthesis and biological evaluation of structural analogues of compactin and dihydromevinolin. Journal of Medicinal Chemistry. 30: 1858-73. PMID 3656359 DOI: 10.1021/Jm00393A030 |
0.396 |
|
| 1987 |
Heathcock CH, Geldern TWv. Total synthesis of (+)-norsecurinine Heterocycles. 25: 75-78. DOI: 10.3987/S-1987-01-0075 |
0.417 |
|
| 1987 |
Hansen MM, Bartlett PA, Heathcock CH. Preparation and reactions of an alkylzinc enolate Organometallics. 6: 2069-2074. DOI: 10.1021/Om00153A006 |
0.406 |
|
| 1987 |
Kerwin SM, Paul AG, Heathcock CH. Quassinoid synthesis. 2. Preparation of a tetracyclic intermediate having the bruceantin tetrahydrofuran ring Journal of Organic Chemistry. 52: 1686-1695. DOI: 10.1021/Jo00385A008 |
0.651 |
|
| 1987 |
Ruggeri RB, Heathcock CH. Synthesis of polycyclic lactam and lactone ethers by intramolecular reformatsky reactions. A model for construction of the daphnilactone a ring system Journal of Organic Chemistry. 52: 5745-5746. DOI: 10.1021/Jo00235A020 |
0.384 |
|
| 1987 |
Hecker S, Heathcock C. Correction. Total Synthesis of (+)-Dihydromevinolin Journal of the American Chemical Society. 109: 7583-7583. DOI: 10.1021/Ja00258A600 |
0.386 |
|
| 1987 |
Lodge EP, Heathcock CH. Acyclic stereoselection. 40. Steric effects, as well as .sigma.*-orbital energies, are important in diastereoface differentiation in additions to chiral aldehydes Journal of the American Chemical Society. 109: 3353-3361. DOI: 10.1021/Ja00245A027 |
0.349 |
|
| 1987 |
Lodge EP, Heathcock CH. Acyclic stereoselection. 39. The origin of diastereofacial selectivity in additions to chiral aldehydes and ketones: trajectory analysis Journal of the American Chemical Society. 109: 2819-2820. DOI: 10.1021/Ja00243A042 |
0.368 |
|
| 1987 |
Burkhardt ER, Doney JJ, Bergman RG, Heathcock CH. Tungsten and molybdenum 2-oxaallyl [.eta.1-(C)-enolate] complexes: functional group transformations, photochemical aldol reactions, and alkyne/carbon monoxide migratory insertion reactions Journal of the American Chemical Society. 109: 2022-2039. DOI: 10.1021/Ja00241A020 |
0.367 |
|
| 1987 |
Oare DA, Heathcock CH. Influence of enolate geometry on the stereochemistry of Michael additions of ketone enolates to α,β-unsaturated ketones Tetrahedron Letters. 28: 1354. DOI: 10.1016/S0040-4039(00)85424-6 |
0.775 |
|
| 1987 |
OARE DA, HEATHCOCK CH. ChemInform Abstract: Acyclic Stereoselection. Part 38. Influence of Enolate Geometry on the Stereochemistry of Michael Additions of Ketone Enolates to α,β-Unsaturated Ketones. Cheminform. 18. DOI: 10.1002/chin.198725063 |
0.754 |
|
| 1987 |
HEATHCOCK CH, RADEL PA. ChemInform Abstract: Acyclic Stereoselection. Part 37. Total Synthesis of a Slightly Unnatural Product. Confirmation of the Stereostructure of the Archaebacterial C40 Diol by Synthesis of a Stereoisomer. Cheminform. 18. DOI: 10.1002/chin.198717320 |
0.323 |
|
| 1986 |
Heathcock CH, Radel PA. Total synthesis of a slightly unnatural product. Confirmation of the stereostructure of the archaebacterial C40 diol by synthesis of a stereoisomer Journal of Organic Chemistry. 51: 4322-4323. DOI: 10.1021/Jo00372A051 |
0.37 |
|
| 1986 |
Heathcock CH, Davidsen SK, Hug KT, Flippin LA. Acyclic stereoselection. XXXVI: Simple diastereoselection in the Lewis acid mediated reactions of enol silanes with aldehydes Journal of Organic Chemistry. 51: 3027-3037. DOI: 10.1021/Jo00365A033 |
0.447 |
|
| 1986 |
Heathcock CH, Uehling DE. Acyclic stereoselection. Part 34. Stereoselection in the Michael addition reaction. 4. Diastereofacial preferences in Lewis acid-mediated additions of enolsilanes to chiral enones The Journal of Organic Chemistry. 51: 279-280. DOI: 10.1021/Jo00352A040 |
0.446 |
|
| 1986 |
Heathcock CH, Davidsen SK, Mills S, Sanner MA. Total synthesis of (.+-.)-methyl homodaphniphyllate Journal of the American Chemical Society. 108: 5650-5651. DOI: 10.1021/Ja00278A061 |
0.384 |
|
| 1986 |
Heathcock CH, Smith KM, Blumenkopf TA. Total synthesis of (±)-fawcettimine (Burnell's base A) Journal of the American Chemical Society. 108: 5022-5024. DOI: 10.1021/Ja00276A062 |
0.343 |
|
| 1986 |
Heathcock CH, Davidsen SK, Hug KT, Flippin LA. Acyclic stereoselection. 36. Simple diastereoselection in the Lewis acid mediated reactions of enol silanes with aldehydes Journal of Organic Chemistry. 51: 3027-3037. DOI: 10.1016/S0040-4039(01)81736-6 |
0.438 |
|
| 1986 |
Rosen T, Heathcock CH. The synthesis of mevinic acids Tetrahedron. 42: 4909-4951. DOI: 10.1016/S0040-4020(01)88045-5 |
0.304 |
|
| 1986 |
Hecker SJ, Heathcock CH. Total synthesis of (+)-dihydromevinolin Journal of the American Chemical Society. 108: 4586-4594. DOI: 10.1002/Chin.198648343 |
0.417 |
|
| 1986 |
HEATHCOCK CH, UEHLING DE. ChemInform Abstract: Acyclic Stereoselection. Part 34. Stereoselection in the Michael Addition Reactions. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198627088 |
0.342 |
|
| 1986 |
Takai K, Heathcock CH. Acyclic Stereoselection. Part 32. Synthesis and Characterization of the Diastereomeric (4S)‐Pentane‐1,2,3,4‐tetrols. Cheminform. 17. DOI: 10.1002/Chin.198601076 |
0.4 |
|
| 1986 |
Heathcock CH, Uehling DE. Stereoselection in the Michael addition reaction. 4. Diastereofacial preferences in Lewis acid mediated additions of enolsilanes to chiral enones Journal of Organic Chemistry. 51: 279-280. |
0.331 |
|
| 1985 |
Hecker SJ, Heathcock CH. An approach to the synthesis of mevinolin based on intramolecular Diels-Alder cycloaddition Journal of Organic Chemistry. 50: 5159-5166. DOI: 10.1021/Jo00225A037 |
0.398 |
|
| 1985 |
Takai K, Heathcock CH. Acyclic stereoselection. 32. Synthesis and characterization of the diastereomeric (4S)-pentane-1,2,3,4-tetrols Journal of Organic Chemistry. 50: 3247-3251. DOI: 10.1021/Jo00218A001 |
0.395 |
|
| 1985 |
Heathcock CH, Oare DA. Acyclic stereoselection. 31. Stereoselection in the Michael addition reaction. 3. Relationship between ester enolate geometry and adduct stereochemistry in the kinetic Michael reaction of lithium enolates with enones Journal of Organic Chemistry. 50: 3022-3024. DOI: 10.1021/Jo00216A051 |
0.779 |
|
| 1985 |
Heathcock CH, Henderson MA, Oare DA, Sanner MA. Acyclic stereoselection. 30. Stereoselection in the Michael addition reaction. 2. Stereochemistry of the kinetic Michael reaction of amide enolates with enones The Journal of Organic Chemistry. 50: 3019-3022. DOI: 10.1021/Jo00216A050 |
0.768 |
|
| 1985 |
Rosen T, Heathcock CH. Synthetic and biological studies of compactin and related compounds. 4. Total synthesis of (+)-compactin Journal of the American Chemical Society. 107: 3731-3733. DOI: 10.1021/Ja00298A062 |
0.369 |
|
| 1985 |
Doney JJ, Bergman RG, Heathcock CH. Synthesis, structure, and carbon-carbon bond-forming reactions of carbon-bound molybdenum, tungsten, and rhenium enolates. Detection of an .eta.3-oxaallyl intermediate Journal of the American Chemical Society. 107: 3724-3726. DOI: 10.1021/Ja00298A057 |
0.327 |
|
| 1985 |
Heathcock CH, Norman MH, Uehling DE. Acyclic stereoselection. 29. Stereoselection in the Michael addition reaction. 1. The Mukaiyama-Michael reaction Journal of the American Chemical Society. 107: 2797-2799. DOI: 10.1021/Ja00295A037 |
0.412 |
|
| 1985 |
Heathcock CH, Montgomery SH. Acyclic stereoselection. 28. Use of stereoselective aldol methodology in the total synthesis of cladinose. Tetrahedron Letters. 26: 1001-1004. DOI: 10.1016/S0040-4039(00)98496-X |
0.453 |
|
| 1985 |
Heathcock CH, Arseniyadis S. Acyclic stereoselection. 35. Effect of cation on diastereofacial selectivity in aldol reactions of a chiral α-silyloxy ketone Tetrahedron Letters. 26: 6009-6012. DOI: 10.1016/S0040-4039(00)95111-6 |
0.442 |
|
| 1985 |
Heathcock CH, Doney JJ, Bergman RG. Synthesis and carbon-carbon bond-forming reactions of tungsten, molybdenum, and rhenium enolates Pure and Applied Chemistry. 57: 1789-1798. DOI: 10.1002/Chin.198614380 |
0.336 |
|
| 1985 |
Connolly PJ, Heathcock CH. An approach to the total synthesis of dendrobine Journal of Organic Chemistry. 50: 4135-4144. DOI: 10.1002/Chin.198610368 |
0.344 |
|
| 1985 |
Heathcock CH, Oare DA. Acyclic Stereoselection. 31. Stereoselection In The Michael Addition Reaction. 3. Relationship Between Ester Enolate Geometry And Adduct Stereochemistry In The Kinetic Michael Reaction Of Lithium Enolates With Enones Cheminform. 16. DOI: 10.1002/Chin.198551087 |
0.796 |
|
| 1985 |
Heathcock CH, Young SD, Hagen JP, Pilli R, Badertscher U. Acyclic stereoselection. 25. Stereoselective synthesis of the C-1 to C-7 moiety of erythronolide A Journal of Organic Chemistry. 50: 2095-2105. DOI: 10.1002/Chin.198547330 |
0.595 |
|
| 1985 |
HEATHCOCK CH, NORMAN MH, UEHLING DE. ChemInform Abstract: ACYCLIC STEREOSELECTION. 29. STEREOSELECTION IN THE MICHAEL ADDITION REACTION. 1. THE MUKAIYAMA-MICHAEL REACTION Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198536086 |
0.307 |
|
| 1985 |
Heathcock CH, Von Geldern TW, Lebrilla CB, Maier WF. Nucleophilic substitution with inversion of configuration at the nucleophile Journal of Organic Chemistry. 50: 968-972. DOI: 10.1002/Chin.198535174 |
0.426 |
|
| 1985 |
Rosen T, Taschner MJ, Thomas JA, Heathcock CH. Synthetic and biological studies of compactin and related compounds. 3. Synthesis of the hexalin portion of compactin Journal of Organic Chemistry. 50: 1190-1201. DOI: 10.1002/Chin.198535148 |
0.337 |
|
| 1985 |
Rosen T, Heathcock CH. Total synthesis of (+)-compactin Journal of the American Chemical Society. 107: 3731-3733. |
0.302 |
|
| 1985 |
Heathcock CH, Oare DA. Stereoselection in the Michael addition reaction. 3. Relationship between ester enolate geometry and adduct stereochemistry in the kinetic Michael reaction of lithium enolates with enones Journal of Organic Chemistry. 50: 3022-3024. |
0.781 |
|
| 1984 |
Heathcock CH, Pirrung MC, Young SD, Hagen JP, Jarvi ET, Badertscher U, Märki HP, Montgomery SH. Acyclic stereoselection. 23. Lactaldehyde enolate equivalents Journal of the American Chemical Society. 106: 8161-8174. DOI: 10.1021/Ja00338A027 |
0.655 |
|
| 1984 |
Heathcock CH, Hug KT, Flippin LA. Acyclic stereoselection. 27. Simple diastereoselection in the lewis acid mediated reactions of enolsilanes with aldehydes Tetrahedron Letters. 25: 5973-5976. DOI: 10.1016/S0040-4039(01)81736-6 |
0.326 |
|
| 1984 |
Kiyooka Si, Sasaoka H, Fujiyama R, Heathcock CH. Diastereofacial selectivity in the Lewis acid mediated reactions of allylsilane with chiral β-alkoxy acetal Tetrahedron Letters. 25: 5331-5334. DOI: 10.1016/S0040-4039(01)81596-3 |
0.39 |
|
| 1984 |
Heathcock CH, Jarvi ET, Rosen T. Acyclic stereoselection. 21. Synthesis of an ionophore synthon having four asymmetric carbons by sequential aldol addition, claisen rearrangement and hydroboration Tetrahedron Letters. 25: 243-246. DOI: 10.1016/S0040-4039(00)99851-4 |
0.399 |
|
| 1984 |
Heathcock CH, Kiyooka SI, Blumenkopf TA. Acyclic stereoselection. 22. Diastereofacial selectivity in the Lewis acid mediated reactions of allylsilanes with chiral aldehydes and enones Journal of Organic Chemistry. 49: 4214-4223. DOI: 10.1002/Chin.198519094 |
0.431 |
|
| 1984 |
Rosen T, Taschner MJ, Heathcock CH. Synthetic and biological studies of compactin and related compounds. 2. Synthesis of the lactone moiety of compactin Journal of Organic Chemistry. 49: 3994-4003. DOI: 10.1002/Chin.198515272 |
0.354 |
|
| 1984 |
HEATHCOCK CH. ChemInform Abstract: Stereoselective Aldol Condensations Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198449357 |
0.301 |
|
| 1984 |
HEATHCOCK CH, MONTGOMERY SH. ChemInform Abstract: ACYCLIC STEREOSELECTION. 19. TOTAL SYNTHESIS OF (.+-.)-RISTOSAMINE AND (.+-.)-MEGALOSAMINE Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198407309 |
0.347 |
|
| 1983 |
Heathcock CH, Jennings RA, Von Geldern TW. Studies directed toward the total synthesis of securinega alkaloids Journal of Organic Chemistry. 48: 3428-3431. DOI: 10.1021/Jo00168A011 |
0.345 |
|
| 1983 |
Blumenkopf TA, Heathcock CH. Stereochemistry of the Sakurai reaction. Additions to cyclohexenones and cycloheptenones Journal of the American Chemical Society. 105: 2354-2358. DOI: 10.1021/Ja00346A041 |
0.393 |
|
| 1983 |
Heathcock CH, Flippin LA. Acyclic stereoselection. 16. High diastereofacial selectivity in Lewis acid mediated additions of enolsilanes to chiral aldehydes Journal of the American Chemical Society. 105: 1667-1668. DOI: 10.1021/Ja00344A050 |
0.371 |
|
| 1983 |
Kiyooka Si, Heathcock CH. Acyclic stereoselection. 20. High diastereofacial selectivity in the stannic chloride mediated reactions of allylsilanes with chiral α- and β-alkoxy aldehydes Tetrahedron Letters. 24: 4765-4768. DOI: 10.1016/S0040-4039(00)94002-4 |
0.366 |
|
| 1983 |
Heathcock CH, Montgomery SH. Acyclic stereoselection. 19. Total synthesis of (±)-ristosamine and (±)-megalosamine. Tetrahedron Letters. 24: 4637-4640. DOI: 10.1016/S0040-4039(00)86214-0 |
0.322 |
|
| 1983 |
Heathcock CH, Lampe J. Acyclic stereoselection. 17. Simple diastereoselection in the addition of medium- and long-chain n-alkyl ketone lithium enolates to aldehydes Journal of Organic Chemistry. 48: 4330-4337. DOI: 10.1002/Chin.198418091 |
0.361 |
|
| 1982 |
Heathcock CH, Tice CM, Germroth TC. Synthesis of sesquiterpene antitumor lactones. 10. Total synthesis of (.+-.)-parthenin Journal of the American Chemical Society. 104: 6081-6091. DOI: 10.1021/Ja00386A040 |
0.438 |
|
| 1982 |
Heathcock CH, DelMar EG, Graham SL. Synthesis of sesqui terpene anti tumor lactones 9. the hydro naphthalene route to pseudo guaianes total synthesis of racemic confertin Journal of the American Chemical Society. 104: 1907-1917. DOI: 10.1021/Ja00371A020 |
0.364 |
|
| 1982 |
Heathcock CH, Kleinman EF, Binkley ES. Total synthesis of lycopodium alkaloids: (.+-.)-lycopodine, (.+-.)-lycodine, and (.+-.)-lycodoline Journal of the American Chemical Society. 104: 1054-1068. DOI: 10.1021/Ja00368A024 |
0.424 |
|
| 1982 |
Heathcock CH, Jarvi ET. Acyclic stereoselection. 15. Sequential aldol-claisen as a method for 1,5-stereoselection. Total synthesis of the vitamin-E side chain Tetrahedron Letters. 23: 2825-2828. DOI: 10.1016/S0040-4039(00)88423-3 |
0.398 |
|
| 1982 |
Heathcock CH, Taschner MJ, Rosen T, A. Thomas J, Hadley CR, Popják G. Synthesis and biological activity of the hexalin moiety of compactin (ML-236B) Tetrahedron Letters. 23: 4747-4750. DOI: 10.1016/S0040-4039(00)85703-2 |
0.306 |
|
| 1982 |
Heathcock CH, DelMar EG, Graham SL. Synthesis of sesquiterpene antitumor lactones. 9. The hydronaphthalene route to pseudoguaianes. Total synthesis of (±)-confertin Journal of the American Chemical Society. 104: 1907-1917. DOI: 10.1002/Chin.198231297 |
0.358 |
|
| 1981 |
Heathcock CH. Acyclic stereocontrol through the aldol condensation. Science (New York, N.Y.). 214: 395-400. PMID 17730226 DOI: 10.1002/Chin.198209364 |
0.372 |
|
| 1981 |
Heathcock CH, Pirrung MC, Lampe J, Buse CT, Young SD. Acyclic stereoselection. 12. Double stereodifferentiation with mutual kinetic resolution. A superior class of reagents for control of Cram's rule stereoselection in synthesis of erythro-.alpha.-alkyl-.beta.-hydroxy carboxylic acids from chiral aldehydes Journal of Organic Chemistry. 46: 2290-2300. DOI: 10.1021/Jo00324A017 |
0.717 |
|
| 1981 |
Heathcock CH, White CT, Morrison JJ, VanDerveer D. Acyclic stereoselection. 11. Double stereodifferentiation as a method for achieving superior Cram's rule selectivity in aldol condensations with chiral aldehydes Journal of Organic Chemistry. 46: 1296-1309. DOI: 10.1021/Jo00320A014 |
0.336 |
|
| 1981 |
White CT, Heathcock CH. Acyclic stereoselection. 10. A general synthesis of erythro-.alpha.-alkyl-.beta.-hydroxy ketones The Journal of Organic Chemistry. 46: 191-192. DOI: 10.1021/Jo00314A047 |
0.371 |
|
| 1981 |
Tice CM, Heathcock CH. Synthesis of sesquiterpene antitumor lactones. 8. An approach to the synthesis of pseudoguianolides based on oxy-Cope rearrangement Journal of Organic Chemistry. 46: 9-13. DOI: 10.1021/Jo00314A003 |
0.409 |
|
| 1981 |
Heathcock CH, Hagen JP, Jarvi ET, Pirrung MC, Young SD. Acyclic stereoselection. 14. O-alkyllactic acid esters: reagents for the stereoselective construction of erythro- and threo-.alpha.-methyl-.alpha.,.beta.-dihydroxy carbonyl compounds Journal of the American Chemical Society. 103: 4972-4974. DOI: 10.1021/Ja00406A064 |
0.679 |
|
| 1981 |
Heathcock CH, Kleinman EF. Total synthesis of (.+-.)-lycodoline Journal of the American Chemical Society. 103: 222-223. DOI: 10.1021/Ja00391A055 |
0.417 |
|
| 1981 |
Schinzer D, Heathcock CH. Fluoride-catalyzed conversion of acylsilanes to aldehydes and ketones Tetrahedron Letters. 22: 1881-1884. DOI: 10.1016/S0040-4039(01)90467-8 |
0.347 |
|
| 1981 |
Heathcock CH, Pirrung MC, Montgomery SH, Lampe J. Acyclic stereoselection-13. Aryl esters: reagents for threo-aldolization Tetrahedron. 37: 4087-4095. DOI: 10.1016/S0040-4020(01)93284-3 |
0.736 |
|
| 1981 |
Heathcock CH, Pirrung MC, Lampe J, Buse CT, Young SD. Acyclic stereoselection. 12. Double stereodifferentiation with mutual kinetic resolution. A superior class of reagents for control of Cram's rule stereoselection in synthesis of erythro-.alpha.-alkyl-.beta.-hydroxy carboxylic acids from chiral aldehydes Cheminform. 12. DOI: 10.1002/Chin.198142079 |
0.717 |
|
| 1981 |
Heathcock CH, Hagen JP, Jarvi ET, Pirrung MC, Young SD. Acyclic stereoselection. 14. O-alkyllactic acid esters: Reagents for the stereoselective construction of erythro- and threo-α-methyl-α,β-dihydroxy carbonyl compounds Journal of the American Chemical Society. 103: 4972-4974. |
0.663 |
|
| 1981 |
Heathcock CH, Pirrung MC, Lampe J, Buse CT, Young SD. Acyclic stereoselection. 12. Double stereodifferentiation with mutual kinetic resolution. A superior class of reagents for control of cram's rule stereoselection in synthesis of erythro-α-alkyl-β-hydroxy carboxylic acids from chiral aldehydes Journal of Organic Chemistry. 46: 2290-2300. |
0.696 |
|
| 1980 |
Dugger RW, Heathcock CH. An Efficient Preparation oftrans, trans-β-Ionylideneacetaldehyde Synthetic Communications. 10: 509-515. DOI: 10.1080/00397918008069326 |
0.413 |
|
| 1980 |
Heathcock CH, Young SD, Hagen JP, Pirrung MC, White CT, VanDerveer D. Acyclic stereoselection. 9. Stereochemistry of the addition of lithium enolates to .alpha.-alkoxy aldehydes Journal of Organic Chemistry. 12: 3846-3856. DOI: 10.1021/Jo01307A023 |
0.679 |
|
| 1980 |
Pirrung MC, Heathcock CH. Acyclic stereoselection. 8. A new class of reagents for the highly stereoselective preparation of threo-2-alkyl-3-hydroxycarboxylic acids by the aldol condensation Journal of Organic Chemistry. 45: 1727-1728. DOI: 10.1021/Jo01297A057 |
0.719 |
|
| 1980 |
Dugger RW, Heathcock CH. A general synthesis of 5,6-dihydro-.alpha.-pyrones The Journal of Organic Chemistry. 45: 1181-1185. DOI: 10.1021/Jo01295A002 |
0.318 |
|
| 1980 |
Heathcock CH, Buse CT, Kleschick WA, Pirrung MC, Sohn JE, Lampe J. Acyclic stereoselection. 7. Stereoselective synthesis of 2-alkyl-3-hydroxy carbonyl compounds by aldol condensation Journal of Organic Chemistry. 45: 1066-1081. DOI: 10.1021/Jo01294A030 |
0.732 |
|
| 1980 |
Heathcock CH, Buse CT, Kleschick WA, Pirrung MC, Sohn JE, Lampe J. Correction. Acyclic Stereoselection. 7. Stereoselective Synthesis of 2-Alkyl-3-hydroxy Carbonyl Compounds by Aldol Condensation Journal of Organic Chemistry. 45: 1066-1081. DOI: 10.1021/Jo00339A601 |
0.73 |
|
| 1980 |
Thomas JA, Heathcock CH. A reagent for cyclohexene annelation Tetrahedron Letters. 21: 3235-3236. DOI: 10.1016/S0040-4039(00)78654-0 |
0.421 |
|
| 1980 |
Graham SL, Heathcock CH. Stereoselectivity in the alkylation of sulfonium salts Tetrahedron Letters. 21: 3865-3868. DOI: 10.1016/0040-4039(80)80201-2 |
0.385 |
|
| 1980 |
Heathcock CH, Pirrung MC, Buse CT, Hagen JP, Young SD, Sohn JE. Acyclic stereoselection. 6. A reagent for achieving high 1,2-diastereoselection in the aldol conversion of chiral aldehydes into 3-hydroxy-2-methylcarboxylic acids Cheminform. 11. DOI: 10.1002/Chin.198007106 |
0.702 |
|
| 1980 |
Heathcock CH, Young SD, Hagen JP, Pirrung MC, White CT, VanDerveer D. Acyclic stereoselection. 9. Stereochemistry of the addition of lithium enolates to α-alkoxy aldehydes Journal of Organic Chemistry. 45: 3846-3856. |
0.674 |
|
| 1979 |
Davalian D, Heathcock CH. Synthesis of 7,8-epoxy-7,8-dihydroretinoids The Journal of Organic Chemistry. 44: 4458-4461. DOI: 10.1021/Jo01338A049 |
0.434 |
|
| 1979 |
Heathcock CH, Pirrung MC, Sohn JE. Acyclic stereoselection. 4. Assignment of stereostructure to .beta.-hydroxycarbonyl compounds by carbon-13 nuclear magnetic resonance The Journal of Organic Chemistry. 44: 4294-4299. DOI: 10.1021/Jo01338A015 |
0.633 |
|
| 1979 |
Heathcock CH, Germroth TC, Graham SL. Stereochemistry of cuprate addition to 4-, 5-, and 6-alkylcycloheptenones The Journal of Organic Chemistry. 44: 4481-4487. DOI: 10.1021/Jo00393A004 |
0.398 |
|
| 1979 |
Heathcock CH, Pirrung MC, Buse CT, Hagen JP, Young SD, Sohn JE. Acyclic stereoselection. 6. A reagent for achieving high 1,2-diastereoselection in the aldol conversion of chiral aldehydes into 3-hydroxy-2-methylcarboxylic acids Journal of the American Chemical Society. 101: 7077-7079. DOI: 10.1021/Ja00517A056 |
0.719 |
|
| 1979 |
Heathcock CH, White CT. Acyclic stereoselection. 5. Use of double stereodifferentiation to enhance 1,2 diastereoselection in aldol condensations of chiral aldehydes Journal of the American Chemical Society. 101: 7076-7077. DOI: 10.1021/Ja00517A055 |
0.395 |
|
| 1979 |
Plavac F, Heathcock CH. Synthesis of sesquiterpene antitumor lactones. 7. Studies directed toward the total synthesis of pentalenolactone. Intramolecular ene reaction. Tetrahedron Letters. 20: 2115-2118. DOI: 10.1016/S0040-4039(01)86277-8 |
0.492 |
|
| 1978 |
Kleschick WA, Heathcock CH. Synthesis and chemistry of ethyl 2-diethylphosphonoacrylate The Journal of Organic Chemistry. 43: 1256-1259. DOI: 10.1021/Jo00400A056 |
0.45 |
|
| 1978 |
Heathcock CH, Kleinman E, Binkley ES. A highly efficient total synthesis of (.+-.)-lycopodine Journal of the American Chemical Society. 100: 8036-8037. DOI: 10.1021/Ja00493A057 |
0.381 |
|
| 1978 |
Buse CT, Heathcock CH. Acyclic stereoselection. III. Synthesis of threo-3-hydroxy-2-methylcarboxylic acids Tetrahedron Letters. 19: 1685-1688. DOI: 10.1016/S0040-4039(01)94640-4 |
0.421 |
|
| 1977 |
Kozar LG, Clark RD, Heathcock CH. Synthesis of bicyclo[2.2.2]octenes and bicyclo[3.2.2]nonenes by .pi.-cyclization The Journal of Organic Chemistry. 42: 1386-1389. DOI: 10.1021/Jo00428A026 |
0.654 |
|
| 1977 |
Buse CT, Heathcock CH. Acyclic stereoselection. 2. Synthesis of 3-hydroxy-2-methyl- and 3-hydroxy-2,4-dimethylcarboxylic acids Journal of the American Chemical Society. 99: 8109-8110. DOI: 10.1021/Ja00466A085 |
0.428 |
|
| 1977 |
Kleschick WA, Buse CT, Heathcock CH. Stereoselection in the aldol condensation Journal of the American Chemical Society. 99: 247-248. DOI: 10.1021/Ja00443A046 |
0.451 |
|
| 1976 |
Clark RD, Heathcock CH. Synthesis of a cytotoxic vernolepin prototype. Ozonization of silyloxyalkenes. The Journal of Organic Chemistry. 41: 1396-403. PMID 1263006 DOI: 10.1002/Chin.197634228 |
0.617 |
|
| 1976 |
Wege PM, Clark RD, Heathcock CH. Synthesis of sesquiterpene antitumor lactones. 6. cis-8a-Vinyloctahydro-3H-2-benzopyran-3,7-dione, a precursor to vernolepin. The Journal of Organic Chemistry. 41: 3144-8. PMID 966107 DOI: 10.1002/Chin.197652369 |
0.546 |
|
| 1976 |
Chavdarian CG, Heathcock CH. Synthesis of Sesquiterpene Anti-Tumor Lactones. IV1. A Stereoselective Synthesis oftrans-2,3-Epoxycyclohexanol Synthetic Communications. 6: 277-280. DOI: 10.1080/00397917608063522 |
0.358 |
|
| 1976 |
Ellis JE, Dutcher JS, Heathcock CH. Pentacyclic triterpene synthesis. 6. Synthesis of a bicyclic intermediate corresponding to rings D and E of .beta.-amyrin The Journal of Organic Chemistry. 41: 2670-2676. DOI: 10.1021/Jo00878A002 |
0.402 |
|
| 1976 |
Dutcher JS, Macmillan JG, Heathcock CH. Pentacyclic triterpene synthesis. 5. Synthesis of optically pure ring AB precursors The Journal of Organic Chemistry. 41: 2663-2669. DOI: 10.1021/Jo00878A001 |
0.395 |
|
| 1976 |
Clark RD, Heathcock CH. Preparation and reactions of .beta.-chloro-.alpha.,.beta.-unsaturated ketones The Journal of Organic Chemistry. 41: 636-643. DOI: 10.1021/Jo00866A012 |
0.557 |
|
| 1976 |
Chavdarian CG, Woo SL, Clark RD, Heathcock CH. Synthesis of sesquiterpene antitumor lactones. V. a model for rings B and C of vernolepin Tetrahedron Letters. 17: 1769-1772. DOI: 10.1016/S0040-4039(00)93778-X |
0.569 |
|
| 1976 |
ELLIS JE, DUTCHER JS, HEATHCOCK CH. ChemInform Abstract: PENTACYCLIC TRITERPENE SYNTHESIS. 6. SYNTHESIS OF A BICYCLIC INTERMEDIATE CORRESPONDING TO RINGS D AND E OF β-AMYRIN Chemischer Informationsdienst. 7: no-no. DOI: 10.1002/Chin.197645370 |
0.42 |
|
| 1975 |
Chavdarian CG, Heathcock CH. Synthesis of delta-lactones from cyclohexenones. Preparation of a vernolepin analog. The Journal of Organic Chemistry. 40: 2970-1. PMID 1177076 DOI: 10.1021/Jo00908A031 |
0.446 |
|
| 1975 |
Clark RD, Kozar LG, Heathcock CH. Cyclopentenones from β, ε-Diketo Phosphonates. Synthesis of cis-Jasmone Synthetic Communications. 5: 1-5. DOI: 10.1080/00397917508063507 |
0.611 |
|
| 1975 |
CLARK RD, KOZAR LG, HEATHCOCK CH. Alkylation of Diethyl 2-Oxoalkanephosphonates Synthesis. 1975: 635-636. DOI: 10.1055/S-1975-23860 |
0.632 |
|
| 1975 |
Clark RD, Heathcock CH. Synthesis of spiro lactones and ketones via conjugate addition to cyclopropyl malonates and β-keto esters Tetrahedron Letters. 16: 529-532. DOI: 10.1016/S0040-4039(00)71912-5 |
0.611 |
|
| 1975 |
CLARK RD, KOZAR LG, HEATHCOCK CH. ChemInform Abstract: CYCLOPENTENONES FROM BETA,EPSILON-DIKETO PHOSPHONATES. SYNTHESIS OF CIS-JASMONE Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197529407 |
0.316 |
|
| 1974 |
Ellis JE, Dutcher JS, Heathcock CH. Pentacyclic Triterpene Synthesis. IV a New Method for Accomplishing Robinson-Nazarov Annelations Synthetic Communications. 4: 71-77. DOI: 10.1080/00397917408062058 |
0.378 |
|
| 1974 |
CLARK RD, HEATHCOCK CH. A New Procedure for the Preparation of β-Chloro-α,β-unsaturated Ketones Synthesis. 1974: 47-48. DOI: 10.1055/S-1974-23238 |
0.54 |
|
| 1974 |
Clark RD, Heathcock CH. Ozonization of silyloxyalkenes Tetrahedron Letters. 15: 2027-2030. DOI: 10.1016/S0040-4039(01)82622-8 |
0.471 |
|
| 1974 |
Clark RD, Heathcock CH. A new synthesis of the vernolepin a-ring Tetrahedron Letters. 15: 1713-1715. DOI: 10.1016/S0040-4039(01)82561-2 |
0.604 |
|
| 1974 |
Dutcher JS, Heathcock CH. Pentacyclic triterpene synthesis. III. Preparation of an optically active synthon for rings A and B Tetrahedron Letters. 15: 933-936. DOI: 10.1016/S0040-4039(01)82372-8 |
0.335 |
|
| 1974 |
Dutcher JS, Macmillan JG, Heathcock CH. Pentacyclic triterpene synthesis. II. Preparation of an AB synthon Tetrahedron Letters. 15: 929-932. DOI: 10.1016/S0040-4039(01)82371-6 |
0.359 |
|
| 1973 |
Brattesani DN, Heathcock CH. A Convenient Procedure for the Alkylation of Acetylenes Synthetic Communications. 3: 245-248. DOI: 10.1080/00397917308065910 |
0.375 |
|
| 1973 |
Clark RD, Ellis JE, Heathcock CH. Methylation of Dimedone Synthetic Communications. 3: 347-354. DOI: 10.1080/00397917308063488 |
0.565 |
|
| 1973 |
Clark RD, Heathcock CH. Reduction of .beta.-halo-.alpha.,.beta.-unsaturated ketones The Journal of Organic Chemistry. 38: 3658-3658. DOI: 10.1021/Jo00960A060 |
0.519 |
|
| 1972 |
Amano Y, Heathcock CH. (+)-Occidentalol: Absolute Stereostructure and Total Synthesis Canadian Journal of Chemistry. 50: 340-345. DOI: 10.1139/V72-051 |
0.409 |
|
| 1972 |
Ratcliffe BE, Heathcock CH. Synthesis and Characterization of S-Methylspiro[4.5]-dec-7-en-6-one and 6-methylspiro[4.5]dec-6-en-8-one Synthetic Communications. 2: 157-163. DOI: 10.1080/00397917208081758 |
0.79 |
|
| 1972 |
Heathcock CH, Ratcliffe R, Van J. Synthesis of hydroazulenes by solvolytic rearrangement of 9-methyl-1-declyl tosylates The Journal of Organic Chemistry. 37: 1796-1807. DOI: 10.1021/Jo00976A029 |
0.398 |
|
| 1972 |
Heathcock CH, Ratcliffe BE. Acid-catalyzed rearrangement of 6-methyltricyclo[4.4.0.02,7]decan-3-one The Journal of Organic Chemistry. 37: 1298-1304. DOI: 10.1021/Jo00974A003 |
0.787 |
|
| 1972 |
Ratcliffe BE, Heathcock CH. Acid-catalyzed rearrangement of tricyclo[4.4.0.2,7]decan-3-ols The Journal of Organic Chemistry. 37: 531-537. DOI: 10.1021/Jo00969A001 |
0.79 |
|
| 1972 |
Heathcock CH, Badger RA. Photochemistry of 1,6-cyclodecadienes. II. Synthesis and photochemistry of 6-methyl-1,6-cyclodecadien-3-one The Journal of Organic Chemistry. 37: 234-238. DOI: 10.1021/Jo00967A013 |
0.788 |
|
| 1972 |
Heathcock CH, Badger RA, Starkey RA. Photochemistry of 1,6-cyclodecadienes. I. 1-Methyl-(E,E)-1,6-cyclodecadiene The Journal of Organic Chemistry. 37: 231-234. DOI: 10.1021/Jo00967A012 |
0.758 |
|
| 1972 |
Heathcock CH, Badger RA, Starkey RH. Correction. Photochemistry of 1,6-Cyclodecadienes. I. 1-Methyl-(E,E)-1,6-cyclodecadiene The Journal of Organic Chemistry. 37: 3754-3754. DOI: 10.1021/Jo00796A619 |
0.758 |
|
| 1972 |
HEATHCOCK CH, ELLIS JE, MCMURRY JE, COPPOLINO A. ChemInform Abstract: SAEURE-KATALYSIERTE ROBINSON-ANNELLIERUNGSRK. Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/Chin.197214260 |
0.594 |
|
| 1971 |
Heathcock CH, Ellis JE. Pentacyclic triterpene synthesis. Preparation of a useful intermediate Journal of the Chemical Society D: Chemical Communications. 1474-1475. DOI: 10.1039/C29710001474 |
0.342 |
|
| 1971 |
Heathcock CH, Ratcliffe R. Stereoselective total synthesis of the guaiazulenic sesquiterpenoids .alpha.-bulnesene and bulnesol Journal of the American Chemical Society. 93: 1746-1757. DOI: 10.1021/Ja00736A029 |
0.338 |
|
| 1971 |
Heathcock CH, Ellis JE, McMurry JE, Coppolino A. Acid-catalyzed Robinson Annelations Tetrahedron Letters. 12: 4995-4996. DOI: 10.1016/S0040-4039(01)97609-9 |
0.627 |
|
| 1970 |
Hassner A, Hoblitt RP, Heathcock C, Kropp JE, Lorber M. Stereochemistry. XLV. Electronic vs. steric effects in the addition of iodine isocyanate to olefins Journal of the American Chemical Society. 92: 1326-1331. DOI: 10.1021/Ja00708A036 |
0.454 |
|
| 1970 |
HASSNER A, HOBLITT RP, HEATHCOCK C, KROPP JE, LORBER M. ChemInform Abstract: ELEKTRONISCHE UND STERISCHE EINFLUESSE BEI DER ADDITION VON JODISOCYANAT AN OLEFINE Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197023122 |
0.519 |
|
| 1969 |
Heathcock CH, Poulter SR. Catalytic hydrogenation of cyclopropyl alkenes. III. On the mechanism of homogeneous hydrogenation in the presence of tris(triphenylphosphine)chlororhodium(I). Tetrahedron Letters. 10: 2755-2758. DOI: 10.1016/S0040-4039(01)88261-7 |
0.751 |
|
| 1969 |
Heathcock CH, Gulick LC, Dehlinger T. Reaction of furyllithium with carboxylic acids Journal of Heterocyclic Chemistry. 6: 141-142. DOI: 10.1002/Jhet.5570060130 |
0.381 |
|
| 1969 |
Heathcock CH, Ellis JE, Badger RA. Reaction of alkyllithium reagents with 2,2-dialkyi-l,3-dioxolanes Journal of Heterocyclic Chemistry. 6: 139-140. DOI: 10.1002/Jhet.5570060129 |
0.779 |
|
| 1969 |
Heathcock CH. A New Synthesis of Alkyl Azides Angewandte Chemie International Edition in English. 8: 134-135. DOI: 10.1002/Anie.196901341 |
0.421 |
|
| 1969 |
Heathcock CH. Neue Synthese für Alkylazide Angewandte Chemie. 81: 148-149. DOI: 10.1002/Ange.19690810405 |
0.348 |
|
| 1968 |
Heathcock CH, Kelly TR. Total synthesis of nor-ketoagarofuran Chemical Communications (London). DOI: 10.1039/C1968000267a |
0.55 |
|
| 1968 |
Heathcock CH, Badger RA. Synthesis and photocyclization of a cyclodecadienone Chemical Communications (London). 1510-1511. DOI: 10.1039/C19680001510 |
0.812 |
|
| 1968 |
Heathcock CH, Ratcliffe BE. Unusual cyclobutane pyrolysis The Journal of Organic Chemistry. 33: 3650-3651. DOI: 10.1021/Jo01273A071 |
0.767 |
|
| 1968 |
Heathcock CH, Poulter SR. The effect of cyclopropyl substitution on the .pi.->.pi.* transition of simple olefins Journal of the American Chemical Society. 90: 3766-3769. DOI: 10.1021/Ja01016A028 |
0.764 |
|
| 1968 |
Poulter SR, Heathcock CH. Catalytic hydrogenation of cyclopropyl alkenes. II. Nature of the intermediates in the heterogeneous hydrogenolysis reaction Tetrahedron Letters. 9: 5343-5347. DOI: 10.1016/S0040-4039(00)75380-9 |
0.784 |
|
| 1968 |
Poulter SR, Heathcock CH. Catalytic hydrogenation of cyclopropyl alkenes. I. Effect of alkyl substitution on the heterogeneous hydrogenolysis reaction Tetrahedron Letters. 9: 5339-5342. DOI: 10.1016/S0040-4039(00)75379-2 |
0.799 |
|
| 1968 |
Heathcock C, Kelly T. Sesquiterpenoids—IV Tetrahedron. 24: 3753-3765. DOI: 10.1016/S0040-4020(01)92007-1 |
0.434 |
|
| 1967 |
Hassner A, Lorber ME, Heathcock C. Addition of iodine isocyanate to olefins. Scope and synthetic utility. The Journal of Organic Chemistry. 32: 540-9. PMID 6042109 DOI: 10.1021/Jo01278A006 |
0.571 |
|
| 1967 |
Heathcock CH, Badger RA, Patterson JW. Total synthesis of (.+-.)-copaene and (.+-.)-ylangene. General method for the synthesis of tricyclo [4.4.0.02,7]decanes Journal of the American Chemical Society. 89: 4133-4145. DOI: 10.1021/Ja00992A032 |
0.804 |
|
| 1966 |
Heathcock CH. The synthesis of 1-methyltricyclo[4.4.0.02,7]decanes Tetrahedron Letters. 7: 2043-2047. DOI: 10.1016/S0040-4039(00)76293-9 |
0.431 |
|
| 1965 |
Hassner A, Heathcock C. Additions and Corrections-On the Mechanism of the Conversion of β-Iodo Carbamates to Aziridines The Journal of Organic Chemistry. 30: 4395-4395. DOI: 10.1021/Jo01023A611 |
0.458 |
|
| 1965 |
Hassner A, Heathcock C. Synthesis and Ring Opening of Fused Steroidal Aziridines*,1 The Journal of Organic Chemistry. 30: 1748-1752. DOI: 10.1021/Jo01017A010 |
0.561 |
|
| 1965 |
Jorgenson MJ, Heathcock CH. Photochemistry of Cyclopropylacrylic Esters Journal of the American Chemical Society. 87: 5264-5266. DOI: 10.1021/Ja00950A060 |
0.399 |
|
| 1964 |
Hassner A, Heathcock C. On the Mechanism of the Conversion of β-Iodo Carbamates to Aziridines1 The Journal of Organic Chemistry. 29: 3640-3645. DOI: 10.1021/Jo01035A052 |
0.445 |
|
| 1964 |
Hassner A, Heathcock C. Reaction of Nitrosyl Chloride with Steroid 5-Enes.1Nuclear Magnetic Resonance as a Stereochemical Tool in Steroids The Journal of Organic Chemistry. 29: 1350-1355. DOI: 10.1021/Jo01029A019 |
0.473 |
|
| 1964 |
Hassner A, Heathcock C. Synthesis of fused ethyleneimines from cyclic olefins Tetrahedron. 20: 1037-1042. DOI: 10.1016/S0040-4020(01)98439-X |
0.349 |
|
| 1963 |
Hassner A, Heathcock C. The stereochemistry of ethyleneimines fused to six-membered rings Tetrahedron Letters. 4: 393-395. DOI: 10.1016/S0040-4039(01)90644-6 |
0.425 |
|
| Show low-probability matches. |
